US20030104526A1

Movatterモバイル変換

Info

Publication number: US20030104526A1
Application number: US09/989,994
Authority: US
Inventors: Qiang Liu
Original assignee: Individual
Current assignee: Sangamo Therapeutics Inc
Priority date: 1999-03-24
Filing date: 2001-11-20
Publication date: 2003-06-05
Also published as: US8524874B2; US20060024726A1; US8383766B2; US7585849B2; US20080242847A1; US20130123484A1; US20060019349A1

Abstract

The specificity of binding of a zinc finger to a triplet or quadruplet nucleotide target subsite depends upon the location of the zinc finger in a multifinger protein and, hence, upon the location of its target subsite within a larger target sequence. The present disclosure provides zinc finger amino acid sequences for recognition of triplet target subsites having the nucleotide G in the 5′-most position of the subsite, that have been optimized with respect to the location of the subsite within the target site. Accordingly, the disclosure provides finger position-specific amino acid sequences for the recognition of GNN target subsites. This allows the construction of multi-finger zinc finger proteins with improved affinity and specificity for their target sequences, as well as enhanced biological activity.

Description

CROSS-REFERENCES TO RELATED APPLICATIONS

The present application is a continuation-in-part of copending U.S. patent application Ser. No. 09/535,008, filed Mar. 23, 2000, which application claims the benefit of U.S. provisional applications No. 60/126,238, filed Mar. 24, 1999, No. 60/126,239 filed Mar. 24, 1999, No. 60/146,595 filed Jul. 30, 1999 and No. 60/146,615 filed Jul. 30, 1999. The present application is also a continuation-in-part of copending U.S. patent application Ser. No. 09/716,637, filed Nov. 20, 2000. The disclosures of all of the aforementioned applications are hereby incorporated by reference in their entireties for all purposes.[0001]

BACKGROUND

Zinc finger proteins (ZFPs) are proteins that can bind to DNA in a sequence-specific manner. Zinc fingers were first identified in the transcription factor TFIIIA from the oocytes of the African clawed toad,[0002]Xenopus laevis. An exemplary motif characterizing one class of these protein (C₂H₂class) is -Cys-(X)_2-4-Cys-(X)₁₂-His-(X)_3-5-His (where X is any amino acid) (SEQ. ID. No:1). A single finger domain is about 30 amino acids in length, and several structural studies have demonstrated that it contains an alpha helix containing the two invariant histidine residues and two invariant cysteine residues in a beta turn co-ordinated through zinc. To date, over 10,000 zinc finger sequences have been identified in several thousand known or putative transcription factors. Zinc finger domains are involved not only in DNA-recognition, but also in RNA binding and in protein-protein binding. Current estimates are that this class of molecules will constitute about 2% of all human genes.

The x-ray crystal structure of Zif268, a three-finger domain from a murine transcription factor, has been solved in complex with a cognate DNA sequence and shows that each finger can be superimposed on the next by a periodic rotation. The structure suggests that each finger interacts independently with DNA over 3 base-pair intervals, with side-chains at positions −1, 2 , 3 and 6 on each recognition helix making contacts with their respective DNA triplet subsites. The amino terminus of Zif268 is situated at the 3′ end of the DNA strand with which it makes most contacts. Some zinc fingers can bind to a fourth base in a target segment. If the strand with which a zinc finger protein makes most contacts is designated the target strand, some zinc finger proteins bind to a three base triplet in the target strand and a fourth base on the nontarget strand. The fourth base is complementary to the base immediately 3′ of the three base subsite.[0003]

The structure of the Zif268-DNA complex also suggested that the DNA sequence specificity of a zinc finger protein might be altered by making amino acid substitutions at the four helix positions (−1, 2, 3 and 6) on each of the zinc finger recognition helices. Phage display experiments using zinc finger combinatorial libraries to test this observation were published in a series of papers in 1994 (Rebar et al.,[0004]Science263, 671-673 (1994); Jamieson et al.,Biochemistry33, 5689-5695 (1994); Choo et al,PNAS91, 11163-11167 (1994)). Combinatorial libraries were constructed with randomized side-chains in either the first or middle finger of Zif268 and then used to select for an altered Zif268 binding site in which the appropriate DNA sub-site was replaced by an altered DNA triplet. Further, correlation between the nature of introduced mutations and the resulting alteration in binding specificity gave rise to a partial set of substitution rules for design of ZFPs with altered binding specificity.

Greisman & Pabo,[0005]Science275, 657-661 (1997) discuss an elaboration of the phage display method in which each finger of a Zif268 was successively randomized and selected for binding to a new triplet sequence. This paper reported selection of ZFPs for a nuclear hormone response element, a p53 target site and a TATA box sequence.

A number of papers have reported attempts to produce ZFPs to modulate particular target sites. For example, Choo et al.,[0006]Nature372, 645 (1994), report an attempt to design a ZFP that would repress expression of a bcr-abl oncogene. The target segment to which the ZFPs would bind was a nine,base sequence 5′GCA GAA GCC3′ chosen to overlap the junction created by a specific oncogenic translocation fusing the genes encoding bcr and abl. The intention was that a ZFP specific to this target site would bind to the oncogene without binding to abl or bcr component genes. The authors used phage display to screen a mini-library of variant ZFPs for binding to this target segment. A variant ZFP thus isolated was then reported to repress expression of a stably transfected bcr-able construct in a cell line.

Pomerantz et al.,[0007]Science267, 93-96 (1995) reported an attempt to design a novel DNA binding protein by fusing two fingers from Zif268 with a homeodomain from Oct-1. The hybrid protein was then fused with a transcriptional activator for expression as a chimeric protein. The chimeric protein was reported to bind a target site representing a hybrid of the subsites of its two components. The authors then constructed a reporter vector containing a luciferase gene operably linked to a promoter and a hybrid site for the chimeric DNA binding protein in proximity to the promoter. The authors reported that their chimeric DNA binding protein could activate expression of the luciferase gene.

Liu et al.,[0008]PNAS94, 5525-5530 (1997) report forming a composite zinc finger protein by using a peptide spacer to link two component zinc finger proteins each having three fingers. The composite protein was then further linked to transcriptional activation domain. It was reported that the resulting chimeric protein bound to a target site formed from the target segments bound by the two component zinc finger proteins. It was further reported that the chimeric zinc finger protein could activate transcription of a reporter gene when its target site was inserted into a reporter plasmid in proximity to a promoter operably linked to the reporter.

Choo et al., WO 98/53058, WO98/53059, and WO 98/53060 (1998) discuss selection of zinc finger proteins to bind to a target site within the HIV Tat gene. Choo et al. also discuss selection of a zinc finger protein to bind to a target site encompassing a site of a common mutation in the oncogene ras. The target site within ras was thus constrained by the position of the mutation.[0009]

Previously-disclosed methods for the design of sequence-specific zinc finger proteins have often been based on modularity of individual zinc fingers; i.e., the ability of a zinc finger to recognize the same target subsite regardless of the location of the finger in a multi-finger protein. Although, in many instances, a zinc finger retains the same sequence specificity regardless of its location within a multi-finger protein; in certain cases, the sequence specificity of a zinc finger depends on its position. For example, it is possible for a finger to recognize a particular triplet sequence when it is present as[0010]finger 1 of a three-finger protein, but to recognize a different triplet sequence when present asfinger 2 of a three-finger protein.

Attempts to address situations in which a zinc finger behaves in a non-modular fashion (i.e., its sequence specificity depends upon its location in a multi-finger protein) have, to date, involved strategies employing randomization of key binding residues in multiple adjacent zinc fingers, followed by selection. See, for example, Isalan et al. (2001)[0011]Nature Biotechnol.19:656-660. However, methods for rational design of polypeptides containing non-modular zinc fingers have not heretofore been described.

SUMMARY

The present disclosure provides compositions comprising and methods involving position dependent recognition of GNN nucleotide triplets by zinc fingers.[0012]

thereby designing a zinc finger protein that binds to a target site.[0015]

Also provided are polypeptides comprising any of zinc finger proteins described herein. In certain embodiments, the polypeptide further comprises at least one functional domain. Also provided are polynucleotides encoding any of the polypeptides described herein. Thus, also provided are nucleic acid encoding zinc fingers, including all of the zinc fingers described above.[0017]

Also provided are segments of a zinc finger comprising a sequence of seven contiguous amino acids as shown herein. Also provided are nucleic acids encoding any of these segments and zinc fingers comprising the same.[0018]

Also provided are zinc finger proteins comprising first, second and third zinc fingers. The first, second and third zinc fingers comprise respectively first, second and third segments of seven contiguous amino acids as shown herein. Also provided are nucleic acids encoding such zinc finger proteins.[0019]

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows results of site selection analysis of two representative zinc finger proteins (leftmost 4 columns) and measurements of binding affinity for each of these proteins to their intended target sequences and to variant target sequences. (rightmost 3 columns). Analysis of ZFP1 is shown in the upper portion of the figure and analysis of ZFP2 is shown in the lower portion of the figure. For the site selection analyses, the amino acid sequences of residues −1 through +6 of the recognition helix of each of the three component zinc fingers (F3, F2 and F1) are shown across the top row; the intended target sequence (divided into finger-specific target subsites) is shown across the second row, and a summary of the sequences bound is shown in the third row. Data for F3 is shown in the second column, data for F2 is shown in the third column, and data for F1 is shown in the third column.[0020]

For the binding affinity analyses, the designed target sequence for each ZFP (“cognate”) and two related sequences (“Mt”) are shown (column 6), along with the K[0021]_dfor binding of the ZFP to each of these sequences (column 7).

FIG. 2 shows amino acid sequences of zinc finger recognition regions (amino acids −1 through +6 of the recognition helix) that bind to each of the 16 GNN triplet subsites. Three amino acid sequences are shown for each trinucleotide subsite; these correspond to optimal amino acid sequences for recognition of the subsite from each of the three positions ([0022]finger 1, F1;finger 2, F2; orfinger 3, F3) in a three-finger zinc finger protein. Amino acid sequences are from N-terminal to C-terminal; nucleotide sequences are from 5′ to 3′.

Also shown are site selection results for each of the 48 position-dependent GNN-recognizing zinc fingers. These show the number of times a particular nucleotide was present, at a given position, in a collection of oligonucleotide sequences bound by the finger. For example, out of 15 oligonucleotides bound by a zinc finger protein with the amino acid sequence QSGHLAR present at the finger 1 (F1) position, 15 contained a G in the 5′-most position of the subsite, 15 contained a G in the middle position of the subsite, while, at the 3′-most position of the subsite, 10 contained an A, 3 contained a G and 2 contained a T. Accordingly, this particular amino acid sequence is optimal for binding a GGA triplet from the F1 position.[0023]

FIGS. 3A, 3B and[0024]3C show site selection data indicating positional dependence of GCA-, GAT- and GGT-binding zinc fingers. The first and fourth (where applicable) rows of each figure show portions of the amino acid sequence of a designed zinc finger protein. Amino acid residues −1 through +6 of each α-helix are listed from left to right. The second and fifth (where applicable) rows show the target sequence, divided into three triplet subsites, one for each finger of the protein shown in the first and fourth (where applicable) rows, respectively. The third and sixth (where applicable) rows show the distribution of nucleotides in the oligonucleotides obtained by site selection with the proteins shown in the first and fourth (where applicable) rows, respectively. FIG. 3A shows data for fingers designed to bind GCA; FIG. 3B shows data for fingers designed to bind GAT; FIG. 3C shows data for fingers designed to bind GGT.

FIGS. 4A and 4B show properties of the engineered ZFP EP2C. FIG. 4A shows site selection data. The first row provides the amino acid sequences of residues −1 through +6 of the recognition helices for each of the three zinc fingers of the EP2C protein. The second row shows the target sequence (5′ to 3′); with the distribution of nucleotides in the oligonucleotides obtained by site selection indicated below the target sequence.[0025]

FIG. 4B shows in vitro and in vivo assays for the binding specificity of EP2C. The first three columns show in vitro measurements of binding affinity of EP2C to its intended target sequence and several related sequences. The first column gives the name of each sequence (2C0 is the intended target sequence, compare to FIG. 4A). The second column shows the nucleotide sequence of various target sequences, with differences from the intended target sequence (2C0) highlighted. The third column shows the K[0026]_d(in nM) for binding of EP2C to each of the target sequences. K_ds were determined by gel shift assays, using 2-fold dilution series of EP2C. The right side of the figure (fourth column and bar graph) shows relative luciferase activities (normalized to β-galactosidase levels) in stable cell lines in which expression of EP2C is inducible. Cells were co-transfected with a vector containing a luciferase coding region under the transcriptional control of the target sequence shown in the same row of the figure, and a control vector encoding β-galactosidase. Luciferase and β-galactosidase levels were measured after induction of EP2C expression. Triplicate samples were assayed and the standard deviations are shown in the bar graph. pGL3 is a luciferase-encoding vector lacking EP2C target sequences. 3B is another negative control, in which luciferase expression is under transcriptional control of sequences (3B) unrelated to the EP2C target sequence.

DEFINITIONS

A zinc finger DNA binding protein is a protein or segment within a larger protein that binds DNA in a sequence-specific manner as a result of stabilization of protein structure through coordination of a zinc ion. The term zinc finger DNA binding protein is often abbreviated as zinc finger protein or ZFP.[0027]

Zinc finger proteins can be engineered to recognize a selected target sequence in a nucleic acid. Any method known in the art or disclosed herein can be used to construct an engineered zinc finger protein or a nucleic acid encoding an engineered zinc finger protein. These include, but are not limited to, rational design, selection methods (e.g., phage display) random mutagenesis, combinatorial libraries, computer design, affinity selection, use of databases matching zinc finger amino acid sequences with target subsite nucleotide sequences, cloning from cDNA and/or genomic libraries, and synthetic constructions. An engineered zinc finger protein can comprise a new combination of naturally-occurring zinc finger sequences. Methods for engineering zinc finger proteins are disclosed in co-owned WO 00/41566 and WO 00/42219; as well as in WO 98/53057; WO 98/53058; WO 98/53059 and WO 98/53060; the disclosures of which are hereby incorporated by reference in their entireties. Methods for identifying preferred target sequences, and for engineering zinc finger proteins to bind to such preferred target sequences, are disclosed in co-owned WO 00/42219.[0028]

A designed zinc finger protein is a protein not occurring in nature whose design/composition results principally from rational criteria. Rational criteria for design include application of substitution rules and computerized algorithms for processing information in a database storing information of existing ZFP designs and binding data.[0029]

A selected zinc finger protein is a protein not found in nature whose production results primarily from an empirical process such as phage display.[0030]

The term naturally-occurring is used to describe an object that can be found in nature as distinct from being artificially produced by man. For example, a polypeptide or polynucleotide sequence that is present in an organism (including viruses) that can be isolated from a source in nature and which has not been intentionally modified by man in the laboratory is naturally-occurring. Generally, the term naturally-occurring refers to an object as present in a non-pathological (undiseased) individual, such as would be typical for the species.[0031]

A nucleic acid is operably linked when it is placed into a functional relationship with another nucleic acid sequence. For instance, a promoter or enhancer is operably linked to a coding sequence if it increases the transcription of the coding sequence. Operably linked means that the DNA sequences being linked are typically contiguous and, where necessary to join two protein coding regions, contiguous and in reading frame. However, since enhancers generally function when separated from the promoter by up to several kilobases or more and intronic sequences may be of variable lengths, some polynucleotide elements may be operably linked but not contiguous.[0032]

A specific binding affinity between, for example, a ZFP and a specific target site means a binding affinity of at least 1×10[0033]⁶M⁻¹.

The terms “modulating expression” “inhibiting expression” and “activating expression” of a gene refer to the ability of a zinc finger protein to activate or inhibit transcription of a gene. Activation includes prevention of subsequent transcriptional inhibition (i.e., prevention of repression of gene expression) and inhibition includes prevention of subsequent transcriptional activation (i.e., prevention of gene activation). Modulation can be assayed by determining any parameter that is indirectly or directly affected by the expression of the target gene. Such parameters include, e.g., changes in RNA or protein levels, changes in protein activity, changes in product levels, changes in downstream gene expression, changes in reporter gene transcription (luciferase, CAT, beta-galactosidase, GFP (see, e.g., Mistili & Spector,[0034]Nature Biotechnology15:961-964 (1997)); changes in signal transduction, phosphorylation and dephosphorylation, receptor-ligand interactions, second messenger concentrations (e.g., cGMP, cAMP, IP3, and Ca2+), cell growth, neovascularization, in vitro, in vivo, and ex vivo. Such functional effects can be measured by any means known to those skilled in the art, e.g., measurement of RNA or protein levels, measurement of RNA stability, identification of downstream or reporter gene expression, e.g., via chemiluminescence, fluorescence, calorimetric reactions, antibody binding, inducible markers, ligand binding assays; changes in intracellular second messengers such as cGMP and inositol triphosphate (IP3); changes in intracellular calcium levels; cytokine release, and the like.

A “regulatory domain” refers to a protein or a protein subsequence that has transcriptional modulation activity. Typically, a regulatory domain is covalently or non-covalently linked to a ZFP to modulate transcription. Alternatively, a ZFP can act alone, without a regulatory domain, or with multiple regulatory domains to modulate transcription.[0035]

A D-able subsite within a target site has the[0036]motif 5′NNGK3′. A target site containing one or more such motifs is sometimes described as a D-able target site. A zinc finger appropriately designed to bind to a D-able subsite is sometimes referred to as a D-able finger. Likewise a zinc finger protein containing at least one finger designed or selected to bind to a target site including at least one D-able subsite is sometimes referred to as a D-able zinc finger protein.

DETAILED DESCRIPTION

I. General[0037]

Tables 1-5 list a collection of nonnaturally occurring zinc finger protein sequences and their corresponding target sites. The first column of each table is an internal reference number. The second column lists a 9 or 10 base target site bound by a three-finger zinc finger protein, with the target sites listed in 5′ to 3′ orientation. The third column provides SEQ ID NOs for the target site sequences listed in[0038]column 2. The fourth, sixth and eighth columns list amino acid residues from the first, second and third fingers, respectively, of a zinc finger protein which recognizes the target sequence listed in the second column. For each finger, seven amino acids, occupying positions −1 to +6 of the finger, are listed. The numbering convention for zinc fingers is defined below.Columns 5, 7 and 9 provide SEQ ID NOs for the amino acid sequences listed incolumns 4, 6 and 8, respectively. The final column of each table lists the binding affinity (i.e., the K_din nM) of the zinc finger protein for its target site. Binding affinities are measured as described below.

Each finger binds to a triplet of bases within a corresponding target sequence. The first finger binds to the first triplet starting from the 3′ end of a target site, the second finger binds to the second triplet, and the third finger binds the third (i.e., the 5′-most) triplet of the target sequence. For example, the RSDSLTS finger (SEQ ID NO:646) of SBS# 201 (Table 2) binds to 5′TTG3′, the ERSTLTR finger (SEQ ID NO:851) binds to 5′GCC3′ and the QRADLRR finger (SEQ ID NO:1056) binds to 5′GCA3′.[0039]

Table 6 lists a collection of consensus sequences for zinc fingers and the target sites bound by such sequences. Conventional one letter amino acid codes are used to designate amino acids occupying consensus positions. The symbol “X” designates a nonconsensus position that can in principle be occupied by any amino acid. In most zinc fingers of the C[0040]₂H₂type, binding specificity is principally conferred by residues −1, +2, +3 and +6. Accordingly, consensus sequence determining binding specificity typically include at least these residues. Consensus sequences are useful for designing zinc fingers to bind to a given target sequence. Residues occupying other positions can be selected based on sequences in Tables 1-5, or other known zinc finger sequences. Alternatively, these positions can be randomized with a plurality of candidate amino acids and screened against one or more target sequences to refine binding specificity or improve binding specificity. In general, the same consensus sequence can be used for design of a zinc finger regardless of the relative position of that finger in a multi-finger zinc finger protein. For example, the sequence RXDNXXR can be used to design a N-terminal, central or C-terminal finger of three finger protein. However, some consensus sequences are most suitable for designing a zinc finger to occupy a particular position in a multi-finger protein. For example, the consensus sequence RXDHXXQ is most suitable for designing a C-terminal finger of a three-finger protein.

II. Characteristics of Zinc Finger Proteins[0041]

Zinc finger proteins are formed from zinc finger components. For example, zinc finger proteins can have one to thirty-seven fingers, commonly having 2, 3, 4, 5 or 6 fingers. A zinc finger protein recognizes and binds to a target site (sometimes referred to as a target segment) that represents a relatively small subsequence within a target gene. Each component finger of a zinc finger protein can bind to a subsite within the target site. The subsite includes a triplet of three contiguous bases all on the same strand (sometimes referred to as the target strand). The subsite may or may not also include a fourth base on the opposite strand that is the complement of the base immediately 3′ of the three contiguous bases on the target strand. In many zinc finger proteins, a zinc finger binds to its triplet subsite substantially independently of other fingers in the same zinc finger protein. Accordingly, the binding specificity of zinc finger protein containing multiple fingers is usually approximately the aggregate of the specificities of its component fingers. For example, if a zinc finger protein is formed from first, second and third fingers that individually bind to triplets XXX, YYY, and ZZZ, the binding specificity of the zinc finger protein is 3′XXX YYY ZZZ5′.[0042]

The relative order of fingers in a zinc finger protein from N-terminal to C-terminal determines the relative order of triplets in the 3′ to 5′ direction in the target. For example, if a zinc finger protein comprises from N-terminal to C-terminal first, second and third fingers that individualy bind, respectively, to[0043]triplets 5′ GAC3′, 5′GTA3′ and 5″GGC3′ then the zinc finger protein binds to thetarget segment 3′CAGATGCGG5′. If the zinc finger protein comprises the fingers in another order, for example, second finger, first finger, third finger, then the zinc finger protein binds to a target segment comprising a different permutation of triplets, in this example, 3′ATGCAGCGG5′ (see Berg & Shi,Science271, 1081-1086 (1996)). The assessment of binding properties of a zinc finger protein as the aggregate of its component fingers may, in some cases, be influenced by context-dependent interactions of multiple fingers binding in the same protein.

Two or more zinc finger proteins can be linked to have a target specificity that is the aggregate of that of the component zinc finger proteins (see e.g., Kim & Pabo,[0044]PNAS95, 2812-2817 (1998)). For example, a first zinc finger protein having first, second and third component fingers that respectively bind to XXX, YYY and ZZZ can be linked to a second zinc finger protein having first, second and third component fingers with binding specificities, AAA, BBB and CCC. The binding specificity of the combined first and second proteins is thus 3′XXXYYYZZZ_AAABBBCCC5′, where the underline indicates a short intervening region (typically 0-5 bases of any type). In this situation, the target site can be viewed as comprising two target segments separated by an intervening segment.

Linkage can be accomplished using any of the following peptide linkers. T G E K P: (SEQ. ID. No:2) (Liu et al., 1997, supra.); (G4S)[0045]_n(SEQ. ID. No:3) (Kim et al.,PNAS93, 1156-1160 (1996.); GGRRGGGS; (SEQ. ID. No:4) LRQRDGERP; (SEQ. ID. No:5) LRQKDGGGSERP; (SEQ. ID. No:6) LRQKD(G3S)₂ERP (SEQ. ID. No:7) Alternatively, flexible linkers can be rationally designed using computer programs capable of modeling both DNA-binding sites and the peptides themselves or by phage display methods . In a further variation, noncovalent linkage can be achieved by fusing two zinc finger proteins with domains promoting heterodimer formation of the two zinc finger proteins. For example, one zinc finger protein can be fused with fos and the other with jun (see Barbas et al., WO 95/119431).

Linkage of two zinc finger proteins is advantageous for conferring a unique binding specificity within a mammalian genome. A typical mammalian diploid genome consists of 3×10[0046]⁹bp. Assuming that the four nucleotides A, C, G, and T are randomly distributed, a given 9 bp sequence is present ˜23,000 times. Thus a ZFP recognizing a 9 bp target with absolute specificity would have the potential to bind to ˜23,000 sites within the genome. An 18 bp sequence is present once in 3.4×10¹⁰bp, or about once in a random DNA sequence whose complexity is ten times that of a mammalian genome.

A component finger of zinc finger protein typically contains about 30 amino acids and has the following motif (N—C):[0047]

Cys-(X)_2-4-Cys-X.X.X.X.X.X.X.X.X.X.X.X.-His-(x)_3-5-His (SEQ. ID. No. 8)

The two invariant histidine residues and two invariant cysteine residues in a single beta turn are co-ordinated through zinc (see, e.g., Berg & Shi,[0048]Science271, 1081-1085 (1996)). The above motif shows a numbering convention that is standard in the field for the region of a zinc finger conferring binding specificity. The amino acid on the left (N-terminal side) of the first invariant His residues is assigned the number +6, and other amino acids further to the left are assigned successively decreasing numbers. The alpha helix begins atresidue 1 and extends to the residue following the second conserved histidine. The entire helix is therefore of variable length, between 11 and 13 residues.

The process of designing or selecting a nonmaturally occurring or variant ZFP typically starts with a natural ZFP as a source of framework residues. The process of design or selection serves to define nonconserved positions (i.e., positions −1 to +6) so as to confer a desired binding specificity. One suitable ZFP is the DNA binding domain of the mouse transcription factor Zif268. The DNA binding domain of this protein has the amino acid sequence:[0049]

YACPVESCDRRFSRSDELTRHIRIHTGQKP (F1) (SEQ. ID No:9)[0050]

FQCRICMRNFSRSDHLTTHIRTHTGEKP (F2) (SEQ. ID. No:10)[0051]

FACDICGRKFARSDERKRHTKIHLRQK (F3) SEQ. ID. No:11)[0052]

and binds to a[0053]target 5′GCG TGG GCG 3′ (SEQ ID No:12).

Another suitable natural zinc finger protein as a source of framework residues is Sp-1. The Sp-1 sequence used for construction of zinc finger proteins corresponds to amino acids 531 to 624 in the Sp-1 transcription factor. This sequence is 94 amino acids in length. The amino acid sequence of Sp-1 is as follows:[0054]

PGKKKQHICHIQGCGKVYGKTSHLRAHLRWHTGERP[0055]

FMCTWSYCGKRFTRSDELQRHKRTHTGEKK[0056]

FACPECPKRFMRSDHLSKHIKTHQNKKG (SEQ. ID. No:13)[0057]

Sp-1 binds to a[0058]target site 5′GGG GCG GGG3′ (SEQ ID No:14).

An alternate form of Sp-1, an Sp-1 consensus sequence, has the following amino acid sequence:[0059]

meklngsgd[0060]

PGKKKQHACPECGKSFSKSSHLRAHQRTHTGERP[0061]

YKCPECGKSFSRSDELQRHQRTHTGEKP[0062]

YKCPECGKSFSRSDHLSKHQRTHQNKKG (SEQ. ID. No:15) (lower case letters are a leader sequence from Shi & Berg,[0063]Chemistry andBiology1, 83-89. (1995). The optimal binding sequence for the Sp-1 consensus sequence is 5′GGGGCGGGG3′ (SEQ ID No:16). Other suitable ZFPs are described below.

There are a number of substitution rules that assist rational design of some zinc finger proteins (see Desjarlais & Berg,[0064]PNAS90, 2256-2260 (1993); Choo & Klug,PNAS91, 11163-11167 (1994); Desjarlais & Berg,PNAS89, 7345-7349 (1992); Jamieson et al., supra; Choo et al., WO 98/53057, WO 98/53058; WO 98/53059; WO 98/53060). Many of these rules are supported by site-directed mutagenesis of the three-finger domain of the ubiquitous transcription factor, Sp-1 (Desjarlais and Berg, 1992; 1993). One of these rules is that a 5′ G in a DNA triplet can be bound by a zinc finger incorporating arginine at position 6 of the recognition helix. Another substitution rule is that a G in the middle of a subsite can be recognized by including a histidine residue atposition 3 of a zinc finger. A further substitution rule is that asparagine can be incorporated to recognize A in the middle of triplet, aspartic acid, glutamic acid, serine or threonine can be incorporated to recognize C in the middle of triplet, and amino acids with small side chains such as alanine can be incorporated to recognize T in the middle of triplet. A further substitution rule is that the 3′ base of triplet subsite can be recognized by incorporating the following amino acids at position −1 of the recognition helix: arginine to recognize G, glutamine to recognize A, glutamic acid (or aspartic acid) to recognize C, and threonine to recognize T. Although these substitution rules are useful in designing zinc finger proteins they do not take into account all possible target sites. Furthermore, the assumption underlying the rules, namely that a particular amino acid in a zinc finger is responsible for binding to a particular base in a subsite is only approximate. Context-dependent interactions between proximate amino acids in a finger or binding of multiple amino acids to a single base or vice versa can cause variation of the binding specificities predicted by the existing substitution rules.

The technique of phage display provides a largely empirical means of generating zinc finger proteins with a desired target specificity (see e.g., Rebar, U.S. Pat. No. 5,789,538; Choo et al., WO 96/06166; Barbas et al., WO 95/19431 and WO 98/543111; Jamieson et al., supra). The method can be used in conjunction with, or as an alternative to rational design. The method involves the generation of diverse libraries of mutagenized zinc finger proteins, followed by the isolation of proteins with desired DNA-binding properties using affinity selection methods. To use this method, the experimenter typically proceeds as follows. First, a gene for a zinc finger protein is mutagenized to introduce diversity into regions important for binding specificity and/or affinity. In a typical application, this is accomplished via randomization of a single finger at positions −1, +2, +3, and +6, and sometimes accessory positions such as +1, +5, +8 and +10. Next, the mutagenized gene is cloned into a phage or phagemid vector as a fusion with gene III of a filamentous phage, which encodes the coat protein pIII. The zinc finger gene is inserted between segments of gene III encoding the membrane export signal peptide and the remainder of pIII, so that the zinc finger protein is expressed as an amino-terminal fusion with pIII or in the mature, processed protein. When using phagemid vectors, the mutagenized zinc finger gene may also be fused to a truncated version of gene III encoding, minimally, the C-terminal region required for assembly of pill into the phage particle. The resultant vector library is transformed into[0065]E. coliand used to produce filamentous phage which express variant zinc finger proteins on their surface as fusions with the coat protein pIII. If a phagemid vector is used, then the this step requires superinfection with helper phage. The phage library is then incubated with target DNA site, and affinity selection methods are used to isolate phage which bind target with high affinity from bulk phage. Typically, the DNA target is immobilized on a solid support, which is then washed under conditions sufficient to remove all but the tightest binding phage. After washing, any phage remaining on the support are recovered via elution under conditions which disrupt zinc finger—DNA binding. Recovered phage are used to infect freshE. coli., which is then amplified and used to produce a new batch of phage particles. Selection and amplification are then repeated as many times as is necessary to enrich the phage pool for tight binders such that these may be identified using sequencing and/or screening methods. Although the method is illustrated for pIII fusions, analogous principles can be used to screen ZFP variants as pVIII fusions.

In certain embodiments, the sequence bound by a particular zinc finger protein is determined by conducting binding reactions (see, e.g., conditions for determination of K[0066]_d, infra) between the protein and a pool of randomized double-stranded oligonucleotide sequences. The binding reaction is analyzed by an electrophoretic mobility shift assay (EMSA), in which protein-DNA complexes undergo retarded migration in a gel and can be separated from unbound nucleic acid. Oligonucleotides which have bound the finger are purified from the gel and amplified, for example, by a polymerase chain reaction. The selection (i.e. binding reaction and EMSA analysis) is then repeated as many times as desired, with the selected oligonucleotide sequences. In this way, the binding specificity of a zinc finger protein having a particular amino acid sequence is determined.

Zinc finger proteins are often expressed with a heterologous domain as fusion proteins. Common domains for addition to the ZFP include, e.g., transcription factor domains (activators, repressors, co-activators, co-repressors), silencers, oncogenes (e.g., myc, jun, fos, myb, max, mad, rel, ets, bcl, myb, mos family members etc.); DNA repair enzymes and their associated factors and modifiers; DNA rearrangement enzymes and their associated factors and modifiers; chromatin associated proteins and their modifiers (e.g. kinases, acetylases and deacetylases); and DNA modifying enzymes (e.g., methyltransferases, topoisomerases, helicases, ligases, kinases, phosphatases, polymerases, endonucleases) and their associated factors and modifiers. A preferred domain for fusing with a ZFP when the ZFP is to be used for represssing expression of a target gene is a KRAB repression domain from the human KOX-1 protein (Thiesen et al.,[0067]New Biologist2, 363-374 (1990); Margolin et al.,Proc. Natl. Acad. Sci. USA91, 4509-4513 (1994); Pengue et al.,Nucl. Acids Res.22:2908-2914 (1994); Witzgall et al.,Proc. Natl. Acad. Sci. USA91, 4514-4518 (1994). Preferred domains for achieving activation include the HSV VP16 activation domain (see, e.g., Hagmann et al.,J. Virol.71, 5952-5962 (1997)) nuclear hormone receptors (see, e.g., Torchia et al.,Curr. Opin. Cell. Biol.10:373-383 (1998)); the p65 subunit of nuclear factor kappa B (Bitko & Barik,J. Virol.72:5610-5618 (1998)and Doyle & Hunt,Neuroreport8:2937-2942 (1997)); Liu et al.,Cancer Gene Ther.5:3-28 (1998)), or artificial chimeric functional domains such as VP64 (Seifpal et al.,EMBO J.11, 4961-4968 (1992)).

An important factor in the administration of polypeptide compounds, such as the ZFPs, is ensuring that the polypeptide has the ability to traverse the plasma membrane of a cell, or the membrane of an intra-cellular compartment such as the nucleus. Cellular membranes are composed of lipid-protein bilayers that are freely permeable to small, nonionic lipophilic compounds and are inherently impermeable to polar compounds, macromolecules, and therapeutic or diagnostic agents. However, proteins and other compounds such as liposomes have been described, which have the ability to translocate polypeptides such as ZFPs across a cell membrane.[0068]

For example, “membrane translocation polypeptides” have amphiphilic or hydrophobic amino acid subsequences that have the ability to act as membrane-translocating carriers. In one embodiment, homeodomain proteins have the ability to translocate across cell membranes. The shortest internalizable peptide of a homeodomain protein, Antennapedia, was found to be the third helix of the protein, from amino acid position 43 to 58 (see, e.g., Prochiantz,[0069]Current Opinion in Neurobiology6:629-634 (1996)). Another subsequence, the h (hydrophobic) domain of signal peptides, was found to have similar cell membrane translocation characteristics (see, e.g., Lin et al.,J. Biol. Chem.270:14255-14258 (1995)).

Examples of peptide sequences which can be linked to a ZFP, for facilitating uptake of ZFP into cells, include, but are not limited to: an 11 amino acid peptide of the tat protein of HIV; a 20 residue peptide sequence which corresponds to amino acids 84-103 of the p16 protein (see Fahraeus et al.,[0070]Current Biology6:84 (1996)); the third helix of the 60-amino acid long homeodomain of Antennapedia (Derossi et al.,J. Biol. Chem.269:10444 (1994)); the h region of a signal peptide such as the Kaposi fibroblast growth factor (K-FGF) h region (Lin et al., supra); or the VP22 translocation domain from HSV (Elliot & O'Hare,Cell88:223-233 (1997)). Other suitable chemical moieties that provide enhanced cellular uptake may also be chemically linked to ZFPs.

Toxin molecules also have the ability to transport polypeptides across cell membranes. Often, such molecules are composed of at least two parts (called “binary toxins”): a translocation or binding domain or polypeptide and a separate toxin domain or polypeptide. Typically, the translocation domain or polypeptide binds to a cellular receptor, and then the toxin is transported into the cell. Several bacterial toxins, including[0071]Clostridium perfringensiota toxin, diphtheria toxin (DT), Pseudomonas exotoxin A (PE), pertussis toxin (PT),Bacillus anthracistoxin, and pertussis adenylate cyclase (CYA), have been used in attempts to deliver peptides to the cell cytosol as internal or amino-terminal fusions (Arora et al.,J. Biol. Chem.,268:3334-3341 (1993); Perelle et al.,Infect. Immun.,61:5147-5156 (1993); Stenmark et al.,J. Cell Biol.113:1025-1032 (1991); Donnelly et al.,PNAS90:3530-3534 (1993); Carbonetti et al.,Abstr. Annu. Meet. Am. Soc. Microbiol.95:295 (1995); Sebo et al.,Infect. Immun.63:3851-3857 (1995); Klimpel et al.,PNAS U.S.A.89:10277-10281 (1992); and Novak et al.,J. Biol. Chem.267:17186-17193 1992)).

Such subsequences can be used to translocate ZFPs across a cell membrane. ZFPs can be conveniently fused to or derivatized with such sequences. Typically, the translocation sequence is provided as part of a fusion protein. Optionally, a linker can be used to link the ZFP and the translocation sequence. Any suitable linker can be used, e.g., a peptide linker.[0072]

III. Position Dependence of Subsite Recognition by Zinc Fingers[0073]

A number of the polypeptides disclosed herein have been characterized using the methods disclosed in parent application Ser. No. 09/716,637 (the disclosure of which is hereby incorporated by reference in its entirety); in particular with respect to the effect of their position, within a multi-finger protein, on their sequence specificity. The results of these investigations provide a set of zinc finger sequences that are optimized for recognition of certain triplet target subsites whose 5′-most nucleotide is a G (i.e., GNN triplet subsites). Thus, particular zinc finger sequences which recognize each of the GNN triplet subsites, from each position of a three-finger zinc finger protein, are provided. See FIG. 2. It will be clear to those of skill in the art that the optimized, position-specific zinc finger sequences disclosed herein for recognition of GNN target subsites are not limited to use in three-finger proteins. For example, they are also useful in six-finger proteins, which can be made by linkage of two three-finger proteins.[0074]

A number of zinc finger amino acid sequences which are reported to bind to target subsites in which the 5′-most nucleotide residue is G (i.e., GNN subsites) have recently been disclosed. Segal et al. (1999)[0075]Proc. Natl. Acad. Sci. USA96:2758-2763; Drier et al. (2000)J. Mol. Biol.303:489-502; U.S. Pat. No. 6,140,081. These GNN-binding zinc fingers were obtained by selection offinger 2 sequences from phage display libraries of three-finger proteins, in which certain amino acid residues offinger 2 had been randomized. Due to the manner in which they were selected, it is not clear whether these sequences would have the same target subsite specificity if they were present in the F1 and/or F3 positions.

Use of the methods and compositions disclosed herein has now allowed identification of specific zinc finger sequences that bind each of the 16 GNN triplet subsites, and for the first time, provides zinc finger sequences that are optimized for recognition of these triplet subsites in a position-dependent fashion. Moreover, in vivo studies of these optimized designs reveal that the functionality of a ZFP is correlated with its binding affinity to its target sequence. See Example 6, infra.[0076]

As a result of the discovery, disclosed herein, that sequence recognition by zinc fingers is position-dependent, it is clear that existing design rules will not, in and of themselves, be applicable to every situation in which it is necessary to construct a sequence-specific ZFP. The results disclosed herein show that many zinc fingers that are constructed based on design rules exhibit the sequence specificity predicted by those design rules only at certain finger positions. The position-specific zinc fingers disclosed herein are likely to function more efficiently in vivo and in cultured cells, with fewer nonspecific effects. Highly specific ZFPs, made using position-specific zinc fingers, will be useful tools in studying gene function and will find broad applications in areas as diverse as human therapeutics and plant engineering.[0077]

IV. Production of Zinc Finger Proteins[0078]

ZFP polypeptides and nucleic acids encoding the same can be made using routine techniques in the field of recombinant genetics. Basic texts disclosing the general methods include Sambrook et al.,[0079]Molecular Cloning, A Laboratory Manual(2nd ed. 1989); Kriegler,Gene Transfer and Expression: A Laboratory Manual(1990); andCurrent Protocols in Molecular Biology(Ausubel et al., eds., 1994)). In addition, nucleic acids less than about 100 bases can be custom ordered from any of a variety of commercial sources, such as The Midland Certified Reagent Company (mcrc@oligos.com), The Great American Gene Company (http://www.genco.com), ExpressGen Inc. (www.expressgen.com), Operon Technologies Inc. (Alameda, Calif.). Similarly, peptides can be custom ordered from any of a variety of sources, such as PeptidoGenic (pkim@ccnet.com), HTI Bio-products, inc. (http://www.htibio.com), BMA Biomedicals Ltd (U.K.), Bio.Synthesis, Inc.

Oligonucleotides can be chemically synthesized according to the solid phase phosphoramidite triester method first described by Beaucage & Caruthers,[0080]Tetrahedron Letts.22:1859-1862 (1981), using an automated synthesizer, as described in Van Devanter et al.,Nucleic Acids Res.12:6159-6168 (1984). Purification of oligonucleotides is by either denaturing polyacrylamide gel electrophoresis or by reverse phase HPLC. The sequence of the cloned genes and synthetic oligonucleotides can be verified after cloning using, e.g., the chain termination method for sequencing double-stranded templates of Wallace et al.,Gene16:21-26 (1981).

Two alternative methods are typically used to create the coding sequences required to express newly designed DNA-binding peptides. One protocol is a PCR-based assembly procedure that utilizes six overlapping oligonucleotides (FIG. 1). Three oligonucleotides ([0081]

oligos

1, 3, and 5 in FIG. 1) correspond to “universal” sequences that encode portions of the DNA-binding domain between the recognition helices. These oligonucleotides typically remain constant for all zinc finger constructs. The other three “specific” oligonucleotides (

oligos

2, 4, and 6 in FIG. 1) are designed to encode the recognition helices. These oligonucleotides contain substitutions primarily at positions -1, 2, 3 and 6 on the recognition helices making them specific for each of the different DNA-binding domains.

The PCR synthesis is carried out in two steps. First, a double stranded DNA template is created by combining the six oligonucleotides (three universal, three specific) in a four cycle PCR reaction with a low temperature annealing step, thereby annealing the oligonucleotides to form a DNA “scaffold.” The gaps in the scaffold are filled in by high-fidelity thermostable polymerase, the combination of Taq and Pfu polymerases also suffices. In the second phase of construction, the zinc finger template is amplified by external primers designed to incorporate restriction sites at either end for cloning into a shuttle vector or directly into an expression vector.[0082]

An alternative method of cloning the newly designed DNA-binding proteins relies on annealing complementary oligonucleotides encoding the specific regions of the desired ZFP. This particular application requires that the oligonucleotides be phosphorylated prior to the final ligation step. This is usually performed before setting up the annealing reactions. In brief, the “universal” oligonucleotides encoding the constant regions of the proteins ([0083]

oligos

1, 2 and 3 of above) are annealed with their complementary oligonucleotides. Additionally, the “specific” oligonucleotides encoding the finger recognition helices are annealed with their respective complementary oligonucleotides. These complementary oligos are designed to fill in the region which was previously filled in by polymerase in the above-mentioned protocol. The complementary oligos to thecommon oligos 1 andfinger 3 are engineered to leave overhanging sequences specific for the restriction sites used in cloning into the vector of choice in the following step. The second assembly protocol differs from the initial protocol in the following aspects: the “scaffold” encoding the newly designed ZFP is composed entirely of synthetic DNA thereby eliminating the polymerase fill-in step, additionally the fragment to be cloned into the vector does not require amplification. Lastly, the design of leaving sequence-specific overhangs eliminates the need for restriction enzyme digests of the inserting fragment. Alternatively, changes to ZFP recognition helices can be created using conventional site-directed mutagenesis methods.

Both assembly methods require that the resulting fragment encoding the newly designed ZFP be ligated into a vector. Ultimately, the ZFP-encoding sequence is cloned into an expression vector. Expression vectors that are commonly utilized include, but are not limited to, a modified pMAL-c2 bacterial expression vector (New England BioLabs or an eukaryotic expression vector, pcDNA (Promega). The final constructs are verified by sequence analysis.[0084]

Any suitable method of protein purification known to those of skill in the art can be used to purify ZFPs (see, Ausubel, supra, Sambrook, supra). In addition, any suitable host can be used for expression, e.g., bacterial cells, insect cells, yeast cells, mammalian cells, and the like.[0085]

Expression of a zinc finger protein fused to a maltose binding protein (MBP-ZFP) in bacterial strain JM109 allows for straightforward purification through an amylose column (NEB). High expression levels of the zinc finger chimeric protein can be obtained by induction with IPTG since the MBP-ZFP fusion in the pMal-c2 expression plasmid is under the control of the tac promoter (NEB). Bacteria containing the MBP-ZFP fusion plasmids are inoculated into 2×YT medium containing 10 μM ZnCl2, 0.02% glucose, plus 50 μg/ml ampicillin and shaken at 37° C. At mid-exponential growth IPTG is added to 0.3 mM and the cultures are allowed to shake. After 3 hours the bacteria are harvested by centrifugation, disrupted by sonication or by passage through a french pressure cell or through the use of lysozyme, and insoluble material is removed by centrifugation. The MBP-ZFP proteins are captured on an amylose-bound resin, washed extensively with buffer containing 20 mM Tris-HCl (pH 7.5), 200 mM NaCl, 5 mM DTT and 50 μM ZnC12, then eluted with maltose in essentially the same buffer (purification is based on a standard protocol from NEB). Purified proteins are quantitated and stored for biochemical analysis.[0086]

The dissociation constants of the purified proteins, e.g., Kd, are typically characterized via electrophoretic mobility shift assays (EMSA) (Buratowski & Chodosh, in[0087]Current Protocols in Molecular Biologypp. 12.2.1-12.2.7 (Ausubel ed., 1996)). Affinity is measured by titrating purified protein against a fixed amount of labeled double-stranded oligonucleotide target. The target typically comprises the natural binding site sequence flanked by the 3 bp found in the natural sequence and additional, constant flanking sequences. The natural binding site is typically 9 bp for a three-finger protein and 2×9 bp+intervening bases for a six finger ZFP. The annealed oligonucleotide targets possess a 1base 5′ overhang which allows for efficient labeling of the target with T4 phage polynucleotide kinase. For the assay the target is added at a concentration of 1 nM or lower (the actual concentration is kept at least 10-fold lower than the expected dissociation constant), purified ZFPs are added at various concentrations, and the reaction is allowed to equilibrate for at least 45 min. In addition the reaction mixture also contains 10 mM Tris (pH 7.5), 100 mM KCl, 1 mM MgCl2, 0.1 mM ZnCl2, 5 mM DTT, 10% glycerol, 0.02% BSA. B: in earlier assays poly d(IC) was also added at 10-100 μg/μl.)

The equilibrated reactions are loaded onto a 10% polyacrylamide gel, which has been pre-run for 45 min in Tris/glycine buffer, then bound and unbound labeled target is resolved by electrophoresis at 150V. (alternatively, 10-20% gradient Tris-HCl gels, containing a 4% polyacrylamide stacker, can be used) The dried gels are visualized by autoradiography or phosphorimaging and the apparent Kd is determined by calculating the protein concentration that gives half-maximal binding.[0088]

The assays can also include determining active fractions in the protein preparations. Active fractions are determined by stoichiometric gel shifts where proteins are titrated against a high concentration of target DNA. Titrations are done at 100, 50, and 25% of target (usually at micromolar levels).[0089]

V. Applications of Engineered Zinc Finger Proteins[0090]

ZPFs that bind to a particular target gene, and the nucleic acids encoding them, can be used for a variety of applications. These applications include therapeutic methods in which a ZFP or a nucleic acid encoding it is administered to a subject and used to modulate the expression of a target gene within the subject. See, for example, co-owned WO 00/41566. The modulation can be in the form of repression, for example, when the target gene resides in a pathological infecting microrganisms, or in an endogenous gene of the patient, such as an oncogene or viral receptor, that is contributing to a disease state. Alternatively, the modulation can be in the form of activation when activation of expression or increased expression of an endogenous cellular gene can ameliorate a diseased state. For such applications, ZFPs, or more typically, nucleic acids encoding them are formulated with a pharmaceutically acceptable carrier as a pharmaceutical composition.[0091]

Pharmaceutically acceptable carriers are determined in part by the particular composition being administered, as well as by the particular method used to administer the composition. (see, e.g.,[0092]Remington's Pharmaceutical Sciences,17^thed. 1985)). The ZFPs, alone or in combination with other suitable components, can be made into aerosol formulations (i.e., they can be “nebulized”) to be administered via inhalation. Aerosol formulations can be placed into pressurized acceptable propellants, such as dichlorodifluoromethane, propane, nitrogen, and the like. Formulations suitable for parenteral administration, such as, for example, by intravenous, intramuscular, intradermal, and subcutaneous routes, include aqueous and non-aqueous, isotonic sterile injection solutions, which can contain antioxidants, buffers, bacteriostats, and solutes that render the formulation isotonic with the blood of the intended recipient, and aqueous and non-aqueous sterile suspensions that can include suspending agents, solubilizers, thickening agents, stabilizers, and preservatives. Compositions can be administered, for example, by intravenous infusion, orally, topically, intraperitoneally, intravesically or intrathecally. The formulations of compounds can be presented in unit-dose or multi-dose sealed containers, such as ampules and vials. Injection solutions and suspensions can be prepared from sterile powders, granules, and tablets of the kind previously described.

The dose administered to a patient should be sufficient to effect a beneficial therapeutic response in the patient over time. The dose is determined by the efficacy and K[0093]_dof the particular ZFP employed, the target cell, and the condition of the patient, as well as the body weight or surface area of the patient to be treated. The size of the dose also is determined by the existence, nature, and extent of any adverse side-effects that accompany the administration of a particular compound or vector in a particular patient

In other applications, ZFPs are used in diagnostic methods for sequence specific detection of target nucleic acid in a sample. For example, ZFPs can be used to detect variant alleles associated with a disease or phenotype in patient samples. As an example, ZFPs can be used to detect the presence of particular mRNA species or cDNA in a complex mixtures of mRNAs or cDNAs. As a further example, ZFPs can be used to quantify copy number of a gene in a sample. For example, detection of loss of one copy of a p53 gene in a clinical sample is an indicator of susceptibility to cancer. In a further example, ZFPs are used to detect the presence of pathological microorganisms in clinical samples. This is achieved by using one or more ZFPs specific to genes within the microorganism to be detected. A suitable format for performing diagnostic assays employs ZFPs linked to a domain that allows immobilization of the ZFP on an ELISA plate. The immobilized ZFP is contacted with a sample suspected of containing a target nucleic acid under conditions in which binding can occur. Typically, nucleic acids in the sample are labeled (e.g., in the course of PCR amplification). Alternatively, unlabelled probes can be detected using a second labelled probe. After washing, bound-labelled nucleic acids are detected.[0094]

ZFPs also can be used for assays to determine the phenotype and function of gene expression. Current methodologies for determination of gene function rely primarily upon either overexpression or removing (knocking out completely) the gene of interest from its natural biological setting and observing the effects. The phenotypic effects observed indicate the role of the gene in the biological system.[0095]

One advantage of ZFP-mediated regulation of a gene relative to conventional knockout analysis is that expression of the ZFP can be placed under small molecule control. By controlling expression levels of the ZFPs, one can in turn control the expression levels of a gene regulated by the ZFP to determine what degree of repression or stimulation of expression is required to achieve a given phenotypic or biochemical effect. This approach has particular value for drug development. By putting the ZFP under small molecule control, problems of embryonic lethality and developmental compensation can be avoided by switching on the ZFP repressor at a later stage in mouse development and observing the effects in the adult animal. Transgenic mice having target genes regulated by a ZFP can be produced by integration of the nucleic acid encoding the ZFP at any site in trans to the target gene. Accordingly, homologous recombination is not required for integration of the nucleic acid. Further, because the ZFP is trans-dominant, only one chromosomal copy is needed and therefore functional knock-out animals can be produced without backcrossing.[0096]

All references cited above are hereby incorporated by reference in their entirety for all purposes.[0097]

EXAMPLESExample 1Initial Design of Zinc Finger Proteins and Determination of Binding Affinity

Initial ZFP designs were based on existing design rules, correspondence regimes and ZFP directories, including those disclosed herein (see Tables 1-5) and also in WO 98/53058; WO 98/530059; WO 98/53060 and co-owned U.S. patent application Ser. No. 09/444,241. See also WO 00/42219. Amino acid sequences were conceptually designed using amino acids 532-624 of the human transcription factor Sp1 as a backbone. Polynucleotides encoding designed ZFPs were assembled using a Polymerase Chain Reaction (PCR)-based procedure that utilizes six overlapping oligonucleotides. PCR products were directly cloned cloning into the Tac promoter vector, pMal-c2 (New England Biolabs, Beverly, Mass.) using the KpnI and BamHI restriction sites. The encoded maltose binding protein-ZFP fusion polypeptides were purified according to the manufacturer's procedures (New England Biolabs, Beverly, Mass.). Binding affinity was measured by gel mobility-shift analysis. All of these procedures are described in detail in co-owned WO 00/41566 and WO 00/42219, as well as in Zhang et al. (2000)[0098]J. Biol. Chem.275:33,850-33,860 and Liu et al. (2001)J. Biol. Chem.276:11,323-11,334; the disclosures of which are hereby incorporated by reference in their entireties.

Example 2Optimization of Binding Specificity by Site Selection

Designed ZFPs were tested for binding specificity using site selection methods disclosed in parent application U.S. Ser. No. 09/716,637. Briefly, designed proteins were incubated with a population of labeled, double-stranded oligonucleotides comprising a library of all possible 9- or 10-nucleotide target sequences. Five nanomoles of labeled oligonucleotides were incubated with protein, at a protein concentration 4-fold above its K[0099]_dfor its target sequence. The mixture was subjected to gel electrophoresis, and bound oligonucleotides were identified by mobility shift, and extracted from the gel. The purified bound oligonucleotides were amplified, and the amplification products were used for a subsequent round of selection. At each round of selection, the protein concentration was decreased by 2 fold. After 3-5 rounds of selection, amplification products were cloned into the TOPO TA cloning vector (Invitrogen, Carlsbad, Calif.), and the nucleotide sequences of approximately 20 clones were determined. The identities of the target sites bound by a designed protein were determined from the sequences and expressed as a compilation of subsite binding sequences.

Example 3Comparison of Site Selection Results With Binding Affinity

To test the correlation between site selection results and the affinity of binding of a ZFP to various related targets, site selection experiments were conducted on 2 three-finger ZFPs, denoted ZFP1 and ZFP2, and the site selection results were compared with K[0100]_dmeasurements obtained from quantitative gel-mobility shift assays using the same ZFPs and target sites. Each ZFP was constructed, based on design rules, to bind to a particular nine-nucleotide target sequence (comprising 3 three-nucleotide subsites), as shown in FIG. 1. Site selection results and affinity measurements are also shown in FIG. 1. The site selection results showed that

fingers

1 and 3 of both the ZFP1 and ZFP2 proteins preferentially selected their intended target sequences. However, the second finger of each ZFP preferentially selected subsites other than those to which they were designed to bind (e.g., F2 of ZFP1 was designed to bind TCG, but preferentially selected GTG; F2 of ZFP2 was designed to bind GGT, but preferentially selected GGA).

To confirm the site selection results, binding affinities of ZFP1 and ZFP2 were measured (see Example 1, supra), both to their original target sequences and to new target sequences reflecting the site selection results. For example, the Mt-1 sequence contains two base changes (compared to the original target sequence for ZFP1) which result in a change in the sequence of the[0101]finger 2 subsite to GTG, reflecting thepreferred finger 2 subsite sequence obtained by site selection. In agreement with the site selection results, binding of ZFP1 to the Mt-1 sequence is approximately 4-fold stronger than its binding to the original target sequence (K_dof 12.5 nM compared to a K_dof 50 nM, see FIG. 1).

For ZFP2, the specificity of[0102]finger 2 for the 3′ base of its target subsite was tested, since, although this finger was designed to bind GGT, site selection indicated that it bound preferentially to GGA. Moreover, the site selection results predicted thatfinger 2 of ZFP2 would bind with approximately equal affinity to GGT and GGC. Accordingly, target sequences containing GGA (Mt-3) and GGC (Mt-4) at thefinger 2 subsite were constructed, and binding affinities of ZFP2 to these target sequences, and to its original target sequence (containing GGT at thefinger 2 subsite), were compared. In complete agreement with the site selection results, ZFP2 exhibited the strongest binding affinity for the target sequence containing GGA at thefinger 2 subsite (K_dof 0.5 nM, FIG. 1), and its affinity for target sequences containing either GGT or GGC at thefinger 2 subsite was approximately equal (K_dof 1 nM for both targets, FIG. 1). Accordingly, the site selection method, in addition to being useful for iterative optimization of binding specificity, can also be used as a useful indicator of binding affinity.

Example 4Use of Site Selection to Identify Position-Dependent, GNN-Binding Zinc Fingers

A large number of engineered ZFPs have been evaluated, by site selection, to identify zinc fingers that bind to GNN target subsites. In the course of these studies, it became apparent that the binding specificity of a particular zinc finger sequence is, in some instances, dependent upon the position of the zinc finger in the protein, and hence upon the location of the target subsite within the target sequence. For example, if one wishes to design a three-finger zinc finger protein to bind to a target sequence containing the triplet subsite GAT, it is necessary to know whether this subsite is the first, second or third subsite in the target sequence (i.e., whether the GAT subsite will be bound by the first, second or third finger of the protein). Accordingly, over 110 three-finger zinc finger proteins, containing potential GNN-recognizing zinc fingers in various locations, have been evaluated by site selection experiments. Generally, several zinc finger sequences were designed to recognize each GNN triplet, and each design was tested in each of the F1, F2 and F3 positions through 4 to 6 rounds of selection.[0103]

The results of these analyses, shown in FIG. 2, provide optimal position-dependent zinc finger sequences (the sequences shown represent amino acid residues −1 through +6 of the recognition helix portion of the finger) for recognition of the 16 GNN target subsites, as well as site selection results for these GNN-specific zinc fingers. Optimal amino acid sequences for recognition of each GNN subsite from each of three positions ([0104]finger 1,finger 2 or finger 3) are thereby provided.

GNG-Binding Finger Designs[0105]

The amino acid sequence RSDXLXR (position −1 to +6 of the recognition helix) was found to be optimal for binding to the four GNG triplets, with Asn[0106]⁺³specifying A as the middle nucleotide; His⁺³specifying G as the middle nucleotide; Ala⁺³specifying T as the middle nucleotide; and Asp⁺³specifying cytosine as the middle nucleotide. At the +5 position, Ala, Thr, Ser, and Gln, were tested, and all showed similar specificity profiles by site selection. Interestingly, and in contrast to a previous report (Swirnoff et al. (1995)Mol. Cell. Biol.15:2275-2287), site selection results indicated that three naturally-occurring GCG-binding fingers from zif268 and Sp1, having the amino acid sequences RSDELTR, RSDELQR, and RSDERKR, were not GCG-specific. Rather, each of these fingers selected almost equal numbers of GCG and GTG sequences. Analysis of binding affinity by gel-shift experiments confirmed thatfinger 3 of zif268, having the sequence RSDERKR, binds GCG and GTG with approximately equal affinity.

Position Dependence of GCA-, GAT-, GGT-, GAA- and GCC-Binding Fingers[0107]

Based on existing design rules, the amino acid sequence QSGDLTR (−1 through +6) was tested for its ability to bind the GCA triplet from three positions (F1, F2, and F3) within a three-finger ZFP. FIG. 3A shows that the QSGDLTR sequence bound preferentially to the GCA triplet subsite from the F2 and F3 positions, but not from F1. In fact, the presence of QSGDLTR at the F1 position of three different three-finger ZFPs resulted predominantly in selection of GCT. Accordingly, an attempt was made to redesign this sequence to obtain specificity for GCA from the F1 position. Since the sequence Q[0108]⁻¹G⁺²S⁺³R⁺⁶had previously been selected from a randomized F1 library using GCA as target (Rebar et al. (1994)Science263:671-673), a D (asp) to S (ser) change was made at the +3 residue of this finger. The resulting sequence, QSGSLTR, was tested for its binding specificity by site selection and found to preferentially bind GCA, from the F1 position, in three different ZFPs (see FIG. 2).

The QSGSLTR zinc finger, optimized for recognition of the GCA subsite from the F1 position, was tested for its selectivity when located at the F2 position. Accordingly, two ZFPs, one containing QSGSLTR at[0109]finger 2 and one containing QSGDLTR at finger 2 (both having identical F1 sequences and identical F3 sequences) were tested by site selection. The results indicated that, when used at the F2 position, QSGSLTR bound preferentially to GTA, rather than GCA. Thus, for optimal binding of a GCA triplet subsite from the F1 position, the amino acid sequence QSGSLTR is required; while, for optimal binding of the same subsite sequence from F2 or F3, QSGDLTR should be used. Accordingly, different zinc finger amino acid sequences may be needed to specify a particular triplet subsite sequence, depending upon the location of the subsite within the target sequence and, hence, upon the position of the finger in the protein.

Positional effects were also observed for zinc fingers recognizing GAT and GGT subsites. The zinc finger amino acid sequence QSSNLAR (−1 through +6) is expected to bind to GAT, based on design rules. However, this sequence selected GAT only from the F1 position, and not from the F2 and F3 positions, from which the sequence GAA was preferentially bound (FIG. 3B). Similarly, the amino acid sequence QSSHLTR which, based on design rules, should bind GGT, selected GGT at the F1 position, but not at the F2 and F3 positions, from which it preferentially bound GGA (FIG. 3C). Conversely, the amino acid sequence TSGHLVR has previously been disclosed to recognize the triplet GGT, based on its selection from a randomized library of[0110]zif268 finger 2. U.S. Pat. No. 6,140,081. However, TSGHLVR was not specific for the GGT subsite when located at the F1 position (FIG. 3C). These results indicate that the binding specificity of many fingers is position dependent, and particularly point out that the sequence specificity of a zinc finger selected from a F2 library may be positionally limited.

The results shown in FIG. 2 indicate that recognition of at least GAA and GCC triplets by zinc fingers is also position dependent.[0111]

These positional dependences stand in contrast to earlier published work, which suggested that zinc fingers behaved as independent modules with respect to the sequence specificity of their binding to DNA. Desjarlais et al. (1993)[0112]Proc. Natl. Acad. Sci. USA90:2256-2260.

Example 5Characterization of EP2C

The engineered zinc finger protein EP2C binds to a target sequence, GCGGTGGCT with a dissociation constant (K[0113]_d) of 2 nM. Site selection results indicated that

fingers

1 and 2 are highly specific for their target subsites, whilefinger 3 selects GCG (its intended target subsite) and GTG at approximately equal frequencies (FIG. 4A). To confirm these observations, the binding affinities of EP2C to its cognate target sequence, and to variant target sequences, was measured by standard gel-shift analyses (see Example 1, supra). As standards for comparison, the binding affinities of Sp1 and zif268 to their respective targets were also measured under the same conditions, and were determined to be 40 nM for SP1 (target sequence GGGGCGGGG) and 2 nM for zif268 (target sequence GCGTGGGCG). Measurements of binding affinities confirmed that F3 of EP2C bound GTG and GCG equally well (K_ds of 2 nM), but bound GAG with a two-fold lower affinity (FIG. 4B).Finger 2 was very specific for the GTG triplet, binding 15-fold less tightly to a GGG triplet (compare 2C0 and 2C3 in FIG. 4B).Finger 1 was also very specific for the GCT triplet, it bound with 4-fold lower affinity to a GAT triplet (2C4) and with 2-fold lower affinity to a GCG triplet (2C5). This example shows, once again, the high degree of correlation between site selection results and binding affinities.

Example 6Evaluation of Engineered ZFPs by in vivo Functional Assays

To determine whether a correlation exists between the binding affinity of a engineered ZFP to its target sequence and its functionality in vivo, cell-based reporter gene assays were used to analyze the functional properties of the engineered ZFP EP2C (see Example 5, supra). For these assays, a plasmid encoding the EP2C ZFP, fused to a VP16 transcriptional activation domain, was used to construct a stable cell line (T-Rex-293™, Invitrogen, Carlsbad, Calif.) in which expression of EP2C-VP16 is inducible, as described in Zhang et al., supra. To generate reporter constructs, three tandem copies of the EP2C target site, or its variants (see FIG. 4B, column 2), were inserted between the Mlu I and BglII sites of the pGL3 luciferase-encoding vector (Promega, Madison, Wis.), upstream of the SV40 promoter. Structures of all reporter constructs were confirmed by DNA sequencing.[0114]

Luciferase reporter assays were performed by co-transfection of luciferase reporter construct (200 ng) and pCMV-βgal (100 ng, used as an internal control) into the EP2C cells seeded in 6-well plates. Expression of the EP2C-VP16 transcriptional activator was induced with doxycycline (0.05 ug/ml) 24 h after transfection of reporter constructs. Cell lysates were harvested 40 hours post-transfection, luciferase and β-galactosidase activities were measured by the Dual-Light Reporter Assay System (Tropix, Bedford, Mass.), and luciferase activities were normalized to the co-transfected β-galactosidase activities. The results, shown on the right side of FIG. 4B, showed that the normalized luciferase activity for each reporter construct was well correlated with the in vitro binding affinity of EP2C to the target sequence present in the construct. For example, the target sequences to which EP2C bound with greatest affinity (2C0 and 2C2, K[0115]_dof 2 nM for each) both stimulated the highest levels of luciferase activity, when used to drive luciferase expression in the reporter construct (FIG. 4B). Target sequences to which EP2C bound with 2-fold lower affinity, 2C1 and 2C5 (K_dof 4 nM for each), stimulated roughly half the luciferase activity of the 2C0 and 2C2 targets. The 2C3 and 2C4 sequences, for which EP2C showed the lowest in vitro binding affinities, also yielded the lowest levels of in vivo activity when used to drive luciferase expression.Target 3B, a sequence to which EP2C does not bind, yielded background levels of luciferase activity, similar to those obtained with a luciferase-encoding vector lacking EP2C target sequences (pGL3). Thus there exist good correlations between binding affinity (as determined by K_dmeasurement), binding specificity (as determined by site selection) and in vivo functionality for engineered zinc finger proteins.

TABLE 1


		SEQ		SEQ		SEQ		SEQ	Kd
SBS#	TARGET	ID	F1	ID	F2	ID	F3	ID	(nM)

249	GCGGGGGCG	17	RSDELTR	123	RSDHLSR	229	RSDELRR	335	20

250	GCGGGGGCG	18	RSDELTR	124	RSDHLSR	230	RSDTLKK	336	70

251	GCGGAGGCG	19	RSDELTR	125	RSDNLTR	231	RSDELRR	337	27.5

252	GCGGCCGCG	20	RSDELTR	126	DRSSLTR	232	RSDELRR	338	100

253	GGATGGGGG	21	RSDHLAR	127	RSDHLTT	233	QRAHLAR	339	0.75

256	GCGGGGTCC	22	ERGDLTT	128	RSDHLSR	234	RSDELRR	340	800

258	GCGGGCGGG	23	RSDHLTR	129	ERGHLTR	235	RSDELRR	341	15

259	GCAGAGGAG	24	RSDNLAR	130	RSDNLAR	236	QSGSLTR	342	250

261	GAGGTGGCC	25	ERGTLAR	131	RSDALSR	237	RSDNLSR	343	0.5

262	GCGGGGGCT	26	QSSDLQR	132	RSDHLSR	238	RSDELRR	344	20

263	GCGGGGGCT	27	QSSDLQR	133	RSDHLSR	239	RSDTLKK	345	1

264	GTGGCTGCC	28	DRSSLTR	134	QSSDLQR	240	RSDALAR	346	27

265	GTGGCTGCC	29	ERGTLAR	135	QSSDLQR	241	RSDALAR	347	600

269	GGGGCCGGG	30	RSDHLTR	136	DRSSLTR	242	RSDHLTR	348	5

270	GGGGCCGGG	31	RSDHLTR	137	ERGTLAR	243	RSDHLTR	349	52.5

272	GCAGGGGCC	32	DRSSLTR	138	RSDHLSR	244	QSGSLTR	350	20

337	TGCGGGGCAA	33	RSADLTR	139	RSDHLTR	245	ERQHLAT	351	24

338	TGCGGGGCAA	34	RSADLTR	140	RSDHLTR	246	ERDHLRT	352	8

339	TGCGGGGCAA	35	RSADLTR	141	RSDHLTT	247	ERQHLAT	353	64

340	TGCGGGGCAA	36	RSADLTR	142	RSDHLTT	248	ERDHLRT	354	48

341	TGCGGGGCAA	37	RSADLTR	143	RGDHLKD	249	ERQHLAT	355	1000

342	TGCGGGGCAA	38	RSADLTR	144	RGDHLKD	250	ERDHLRT	356	1000

343	TGCGGGGCAA	39	QSGSLTR	145	RSDHLTR	251	ERQHLAT	357	8

344	TGCGGGGCAA	40	QSGSLTR	146	RSDHLTR	252	ERDHLRT	358	6

345	TGCGGGGCAA	41	QSGSLTR	147	RSDHLTT	253	ERQHLAT	359	96

346	TGCGGGGCAA	42	QSGSLTR	148	RSDHLTT	254	ERDHLRT	360	64

347	TGCGGGGCAA	43	QSGSLTR	149	RGDHLKD	255	ERQHLAT	361	1000

348	TGCGGGGCAA	44	QSGSLTR	150	RGDHLKD	256	ERDHLRT	362	1000

367	GGGGGCGGG	45	RSDHLTR	151	DSGHLTR	257	RSDHLQR	363	60

368	GAGGGGGCG	46	RSDELTR	152	RSDHLTR	258	RSDNLTR	364	3.5

369	GTAGTTGTG	47	RSDALTR	153	TGGSLAR	259	QSGSLTR	365	95

370	GTAGTTGTG	48	RSDALTR	154	NRATLAR	260	QSASLTR	366	300

371	GTAGTTGTG	49	RSDALTR	155	NRATLAR	261	QSGSLTR	367	175

372	GTAGTTGTG	50	RSDSLLR	156	TGGSLAR	262	QSASLTR	368	112.5

373	GTAGTTGTG	51	RSDSLLR	157	NRATLAR	263	QSASLTR	369	320

374	GCTGAGGAA	52	QRSNLVR	158	RSDNLTR	264	TSSELQR	370	3.3

375	GAGGAAGAT	53	QQSNLAR	159	QSGNLQR	265	RSDNLTR	371	85

401	GTAGTTGTG	54	RSDALTR	160	TGGSLAR	266	QSASLTR	372	80

403	GTAGTTGTG	55	RSDSLLR	161	NRATLAR	267	QSGSLTR	373	750

421	GTAGTTGTG	56	DSDSLLR	162	TGGSLAR	268	QSGSLTR	374	500

422	GTAGTTGTG	57	RSDSLLR	163	TGGSLTR	269	QSGSLTR	375	200

423	GTAGTTGTG	58	RSDALTR	164	TGGSLAR	270	QRSALAR	376	1000

424	GATGCTGAG	59	RSDNLTR	165	TSSELQR	271	TSANLSR	377	100

425	GATGCTGAG	60	RSDNLTR	166	QSSDLQR	272	QQSNLAR	378	25

426	GATGCTGAG	61	RSDNLTR	167	QSSDLQR	273	TSANLSR	379	5.5

427	GCTGAGGAA	62	QRSNLVR	168	RSDNLTR	274	QSSDLQR	380	1

428	GAAGATGAC	63	DSSNLTR	169	QQSNLAR	275	QRSNLVR	381	120

429	GAAGATGAC	64	DSSNLTR	170	TSANLSR	276	QRSNLVR	382	50

430	GATGACGAC	65	EKANLTR	171	DSSNLTR	277	QQSNLAR	383	250

431	GACGACGGC	66	DSGHLTR	172	DRSNLER	278	DSSNLTR	384	100

432	GACGACGGC	67	DSGHLTR	173	DHANLAR	279	DSSNLTR	385	1000

433	GACGACGGC	68	DSGNLTR	174	DHANLAR	280	DSSNLTR	386	1000

434	GACGGCGTA	69	QSASLTR	175	DSGHLTR	281	EKANLTR	387	152.5

435	GACGGCGTA	70	QSASLTR	176	DSGHLTR	282	ERGNLTR	388	150

436	GACGGCGTA	71	QRSALAR	177	DSGHLTR	283	EKANLTR	389	95

437	GACGGCGTA	72	QRSALAR	178	DSGHLTR	284	ERGNLTR	390	117.5

438	GAGGGGGCG	73	RSDELTR	179	RSDHLTT	285	RSDNLTR	391	62.5

440	GCCGAGGTGC	74	RSDSLLR	180	RSKNLQR	286	ERGTLAR	392	40

441	GGTGGAGTCA	75	DSGSLTR	181	QSGHLQR	287	TSGHLTR	393	250

445	GTCGCAGTGA	76	RSDSLRR	182	QSSDLQK	288	DSGSLTR	394	1000

450	GACTTGGTGC	77	RSDTLAR	183	RGDALTS	289	DRSNLTR	395	130

453	GGTGGAGTCA	78	DRSALAR	184	QSGHLQR	290	DSSKLSR	396	150

461	GAGTACTGTA	79	QRSHLTT	185	DRSNLRT	291	RSDNLAR	397	120

463	GTGGAGGAGA	80	RSDNLTR	186	RSDNLAR	292	RSDALAR	398	0.5

464	GTGGAGGAGA	81	RSDNLTR	187	RSDNLAR	293	RSDSLAR	399	0.4

466	CAGGCTGCGC	82	RSDDLTR	188	QSSDLQR	294	RSDNLRE	400	65

467	CAGGCTGCGC	83	RSDELTR	189	QSSDLQR	295	RGDHLKD	401	800

468	CAGGCTGCGC	84	RSDDLTR	190	QSSDLQR	296	RGDHLKD	402	42

469	GAAGAGGTCT	85	DRSALAR	191	RSDNLAR	297	QSGNLTR	403	13.5

472	GAGGTCTGGA	86	RSSHLTT	192	DRSALAR	298	RSDNLAR	404	80

476	GGAGAGGATG	87	TTSNLRR	193	RSDNLAR	299	QSDHLTR	405	80

477	GGAGAGGATG	88	TTSNLRR	194	RSDNLAR	300	QRAHLAR	406	100

478	GGAGAGGATG	89	TTSNLRR	195	RSDNLAR	301	QSGHLRR	407	60

479	GTGGCGGACC	90	DSSNLTR	196	RSDELQR	302	RSDALAR	408	8.5

480	GTGGCGGACC	91	DSSNLTR	197	RADTLRR	303	RSDALAR	409	5

483	GAGGGCGAAG	92	QSANLAR	198	ESSKLKR	304	RSDNLAR	410	130

484	GAGGGCGAAG	93	QSDNLAR	199	ESSKLKR	305	RSDNLAR	411	1000

485	GGAGAGGTTT	94	QSSALAR	200	RSDNLAR	306	QRAHLAR	412	110

487	GGAGAGGTTT	95	NRATLAR	201	RSDNLAR	307	QSGHLAR	413	76.9

488	TGGTAGGGGG	96	RSDHLAR	202	RSDNLTT	308	RSDHLTT	414	35

490	TAGGGGGTGG	97	RSDSLLR	203	RSDHLTR	309	RSDNLTT	415	1.5

503	GCCGAGGTGC	98	RSDSLLR	204	RSDNLAR	310	ERGTLAR	416	50

504	GCCGAGGTGC	99	RSDSLLR	205	RSDNLAR	311	DRSDLTR	417	25

505	GCCGAGGTGC	100	RSDSLLR	206	RSDNLAR	312	DCRDLAR	418	65

526	GCGGGCGGGC	101	RSDHLTR	207	ERGHLTR	313	RSDTLKK	419	8

543	GAGTGTGTGA	102	RSDLLQR	208	MSHHLKE	314	RSDHLSR	420	50

544	GAGTGTGTGA	103	RSDSLLR	209	MSHHLKE	315	RSDNLAR	421	125

545	GAGTGTGTGA	104	RKDSLVR	210	TSDHLAS	316	RSDNLTR	422	32

546	GAGTGTGTGA	105	RSDLLQR	211	MSHHLKT	317	RLDGLRT	423	500

547	GAGTGTGTGA	106	RKDSLVR	212	TSGHLTS	318	RSDNLTR	424	500

548	GAGTGTGTGA	107	RSSLLQR	213	MSHHLKT	319	RSDHLSR	425	500

549	GAGTGTGTGA	108	RSSLLQR	214	MSHHLKE	320	RSDHLSR	426	500

550	GAGTGTGTGA	109	RKDSLVR	215	TKDHLAS	321	RSDNKLTR	427	20

551	GAGTGTGTGA	110	RSDLLQR	216	MSHHLKT	322	RSDHLSR	428	50

552	GAGTGTGTGA	111	RKDSLVR	217	MSHHLKT	323	RSDNLTR	429	31

553	GAGTGTGTGA	112	RSDSLLR	218	MSHHLKE	324	RSDNLTR	430	125

554	GAGTGTGTGA	113	RKDSLVR	219	TSDHLAS	325	RSDNLAR	431	62.5

558	TGCGGGGCA	114	QSGDLTR	220	RSDHLTR	326	DSGHLAS	432	21

559	GAGTGTGTGA	115	RSDSLLR	221	TSDHLAS	327	RSDNLAR	433	1000

560	GAGTGTGTGA	116	RSSLLQR	222	MSHHLKT	328	RSDHLSR	434	500

561	GAGTGTGTGA	117	RKDSLVR	223	MSHHLKE	329	RSDNLAR	435	1000

562	GAGTGTGTGA	118	RSDSLLR	224	TSGHLTS	330	RSDNLAR	436	1000

565	GATGCTGAG	119	RSDNLTR	225	TSSELQR	331	QQSNLAR	437	100

567	GAAGATGAC	120	EKANLTR	226	TSANLSR	332	QRSNLVR	438	47.5

568	GATGACGAC	121	EKANLTR	227	DSSNLTR	333	TSANLSR	439	300

569	GTAGTTGTG	122	RSDSLLR	228	TGGSLAR	334	QRSALTR	440	52

[0116]

TABLE 2


		SEQ		SEQ		SEQ		SEQ	Kd
SBS#	TARGET	ID	F1	ID	F2	ID	F3	ID	(nM)

201	GCAGCCTTG	441	RSDSLTS	646	ERSTLTR	851	QRADLRR	1056	1000

202	GCAGCCTTG	442	RSDSLTS	647	ERSTLTR	852	QRADLAR	1057	1000

203	GCAGCCTTG	443	RSDSLTS	648	ERSTLTR	853	QRATLRR	1058	1000

204	GCAGCCTTG	444	RSDSLTS	649	ERSTLTR	854	QRATLAR	1059	1000

205	GAGGTAGAA	445	QSANLAR	650	QSATLAR	855	RSDNLSR	1060	80

206	GAGGTAGAA	446	QSANLAR	651	QSAVLAR	856	RSDNLSR	1061	1000

207	GAGTGGTTA	447	QRASLAS	652	RSDHLTT	857	RSDNLAR	1062	70

208	TAGGTCTTA	448	QRASLAS	653	DRSALAR	858	RSDNLAS	1063	1000

209	GGAGTGGTT	449	QSSALAR	654	RSDALAR	859	QRAHLAR	1064	35

210	GGAGTGGTT	450	NRDTLAR	655	RSDALAR	860	QRAHLAR	1065	65

211	GGAGTGGTT	451	QSSALAR	656	RSDALAS	861	QRAHLAR	1066	140

212	GGAGTGGTT	452	NRDTLAR	657	RSDALAS	862	QRAHLAR	1067	400

213	GTTGCTGGA	453	QRAHLAR	658	QSSTLAR	863	QSSALAR	1068	1000

214	GTTGCTGGA	454	QRAHLAR	659	QSSTLAR	864	NRDTLAR	1069	1000

215	GAAGTCTGT	455	NRDHLMV	660	DRSALAR	865	QSANLSR	1070	1000

216	GAAGTCTGT	456	NRDHLTT	661	DRSALAR	866	QSANLSR	1071	1000

217	GAGGTCGTA	457	QRSALAR	662	DRSALAR	867	RSDNLAR	1072	40

219	GATGTTGAT	458	QQSNLAR	663	NRDTLAR	868	NRDNLSR	1073	1000

220	GATGTTGAT	459	QQSNLAR	664	NRDTLAR	869	QQSNLSR	1074	1000

221	GATGAGTAC	460	DRSNLRT	665	RSDNLAR	870	NRDNLAR	1075	1000

222	GATGAGTAC	461	ERSNLRT	666	RSDNLAR	871	NRDNLAR	1076	1000

223	GATGAGTAC	462	DRSNLRT	667	RSDNLAR	872	QQSNLAR	1077	105

224	GATGAGTAC	463	ERSNLRT	668	RSDNLAR	873	QQSNLAR	1078	1000

225	TGGGAGGTC	464	DRSALAR	669	RSDNLAR	874	RSDHLTT	1079	6

226	GCAGCCTTG	465	RGDALTS	670	ERGTLAR	875	QSGSLTR	1080	1000

227	GCAGCCTTG	466	RGDALTV	671	ERGTLAR	876	QSGSLTR	1081	1000

228	GCAGCCTTG	467	RGDALTM	672	ERGTLAR	877	QSGSLTR	1082	1000

229	GCAGCCTTG	468	RGDALTS	673	ERGTLAR	878	RSDELTR	1083	1000

230	GCAGCCTTG	469	RGDALTV	674	ERGTLAR	879	RSDELTR	1084	1000

231	GCAGCCTTG	470	RGDALTM	675	ERGTLAR	880	RSDELTR	1085	1000

232	GGTGTGGTG	471	RSDALTR	676	RSDALAR	881	NRSHLAR	1086	50

233	GGTGTGGTG	472	RSDALTR	677	RSDALAR	882	QASHLAR	1087	100

235	GTAGAGGTG	473	RSDALTR	678	RSDNLAR	883	QRGALAR	1088	80

236	GGGGAGGGG	474	RSDHLAR	679	RSDNLAR	884	RSDHLSR	1089	0.3

237	GGGGAGGCC	475	ERGTLAR	680	RSDNLAR	885	RSDHLSR	1090	0.3

238	GGGGAGGCC	476	ERGTLAR	681	RSDNLQR	886	RSDHLSR	1091	0.8

239	GGCGGGGAG	477	RSDNLTR	682	RSDHLTR	887	DRSHLAR	1092	0.4

240	GCAGGGGAG	478	RSDNLTR	683	RSDHLSR	888	QSGSLTR	1093	1

242	GGGGGTGCT	479	QSSDLRR	684	QSSHLAR	889	RSDHLSR	1094	1

243	GTGGGCGCT	480	QSSDLRR	685	DRSHLAR	890	RSDALAR	1095	75

244	TAAGAAGGG	481	RSDHLAR	686	QSGNLTR	891	QSGNLRT	1096	100

245	TAAGAAGGG	482	RSDHLAR	687	QSANLTR	892	QSGNLRT	1097	235

246	GAAGGGGAG	483	RSDNLAR	688	RSDHLAR	893	QSGNLTR	1098	2

247	GAAGGGGAG	484	RSDNLAR	689	RSDHLAR	894	QSGNLRR	1099	2

276	GCGGCCGCG	485	RSDELTR	690	ERGTLAR	895	RSDERKR	1100	90

277	GCGGCCGCG	486	RSDELTR	691	DRSSLTR	896	RSDERKR	1101	107

278	GCGGCCGCG	487	QSWELTR	692	ERGTLAR	897	RSDERKR	1102	190

279	GCGGCCGCG	488	QSWELTR	693	DRSSLTR	898	RSDERKR	1103	260

280	GCGGCCGCG	489	QSGSLTR	694	ERGTLAR	899	RSDERKR	1104	160

281	GCGGCCGCG	490	QSGSLTR	695	DRSSLTR	900	RSDERKR	1105	225

282	GCAGAAGTG	491	RGDALTR	696	QSANLTR	901	QSADLAR	1106	1000

283	GCAGAAGTG	492	RSDALTR	697	QSGNLTR	902	QSGSLTR	1107	2

284	GCGGCCGCG	493	QSGSLTR	698	RSDHLTT	903	RSDERKR	1108	1000

285	TGTGCGGCC	494	ERGTLRG	699	RSDELTR	904	SRDHLQS	1109	1000

287	GCAGAAGCG	495	RGPDLAR	700	QSANLTR	905	QSGSLTR	1110	1000

288	GCAGAAGCG	496	RGPDLAR	701	QSANLTR	906	QSGSLTR	1111	1000

289	GCAGAAGCG	497	RGPDLAR	702	QSGNLQR	907	QSGSLTR	1112	800

290	GCAGAAGCG	498	RSDELAR	703	QSANLTR	908	QSADLAR	1113	1000

292	GCAGAAGCG	499	RSDELTR	704	QSANLQR	909	QSGSLTR	1114	1000

293	GTGTGCGGC	500	DRSHLTR	705	ERHSLQT	910	RSDALTR	1115	320

296	TGCGCGGCC	501	ERGTLAR	706	RSDELTR	911	DRDHLQS	1116	1000

297	TGCGCGGCC	502	ERGTLAR	707	RSDELRR	912	DRSHLQT	1117	500

298	GCTTAGGCA	503	QTGELRR	708	RSDNLQK	913	TSGDLSR	1118	4000

299	GCTTAGGCA	504	QTSDLRR	709	RSDNLQK	914	QSSDLQR	1119	4000

300	GCTTAGGCA	505	QTADLRR	710	RSDNLQR	915	QSSDLSR	1120	400

301	GCTTAGGCA	506	QSADLRR	711	RSDNLQT	916	QSSDLSR	1121	350

302	GCTTAGGCA	507	QSGSLTR	712	RSDNLQT	917	QSSDLSR	1122	75

303	GCTTAGGCA	508	QTGSLTR	713	RSDNLQT	918	QSSDLSR	1123	135

304	GCTTAGGCA	509	QTADLTR	714	RSDNLQT	919	QSSDLSR	1124	230

305	GCTTAGGCA	510	QTGDLTR	715	RSDNLQT	920	QSSDLSR	1125	230

306	GCTTAGGCA	511	QTASLTR	716	RSDNLQT	921	QSSDLSR	1126	280

307	GAAGAAGCG	512	RSDELRR	717	QSGNLQR	922	QSGNLSR	1127	50.5

308	GAAGAAGCG	513	RSDELRR	718	QSANLQR	923	QSANLQR	1128	1000

309	GGAGATGCC	514	ERSDLRR	719	QSSNLQR	924	QSGHLSR	1129	4000

310	GGAGATGCC	515	DRSDTTR	720	NRDNLQT	925	QSGHLSR	1130	1000

311	GGAGATGCC	516	DRSTLTR	721	NRDNLQR	926	QSGHLSR	1131	170

312	GGAGATGCC	517	ERGTLAR	722	NRDNLQR	927	QSGHLSR	1132	2000

313	GGAGATGCC	518	DRSDLTR	723	QRSNLQR	928	QSGHLSR	1133	1000

314	GGAGATGCC	519	DRSSLTR	724	QSSNLQR	929	QSGHLSR	1134	117.5

315	GGAGATGCC	520	ERGTLAR	725	QSSNLQR	930	QSGHLSR	1135	265

316	GGAGATGCC	521	ERGTLAR	726	QRDNLQR	931	QSGHLSR	1136	3000

318	TAGGAGATGC	522	RSDALTS	727	RSDNLAR	932	RSDNLAS	1137	100

319	GGGGAAGGG	523	KTSHLRA	728	QSGNLSR	933	RSDHLSR	1138	125

320	GGGGAAGGG	524	RSDHLTR	729	QSGNLSR	934	RSDHLSR	1139	5

321	GGCGGAGAT	525	TTSNLRR	730	QSGHLQR	93S	DRSHLTR	1140	200

323	GGCGGAGAT	526	TTSNLRR	731	QSGHLQR	936	DRDHLTR	1141	600

324	GGCGGAGAT	527	TTSNLRR	732	QSGHLQR	937	DRDHLTR	1142	200

325	GTATCTGCT	528	NSSDLTR	733	NSDVLTS	938	QSDVLTR	1143 1000

326	GTATCTGTT	529	NSDALTR	734	NSDVLTS	939	QSDVLTR	1144	1000

327	TCTGCTGGG	530	RSDHLTR	735	NSADLTR	940	NSDDLTR	1145	1000

328	TCTGTTGGG	531	RSDHLTR	736	NSSALTS	941	NSDDLTR	1146	1000

349	GGTGTCGCC	532	DCRDLAR	737	DSGSLTR	942	TSGHLTR	1147	1000

350	TCCGAGGGT	533	TSGHLTR	738	RSDNLTR	943	DCRDLTT	1148	332

351	GCTGGTGTC	534	DSGSLTR	739	TSGHLTR	944	TLHTLTR	1149	1000

352	GGAGGGGTG	535	RSDSLLR	740	RSDHLTR	945	QSDHLTR	1150	26

353	GTTGGAGCC	536	DCRDLAR	741	QSDHLTR	946	TSGALTR	1151	1000

354	GAAGAGGAC	537	DSSNLTR	742	RSDNLTR	947	QRSNLVR	1152	28

355	GAAGAGGAC	538	EKANLTR	743	RSDNLTR	948	QRSNLVR	1153	20

356	GGCTGGGCG	539	RSDELRR	744	RSDHLTK	949	DSDHLSR	1154	1000

357	GGCTGGGCG	540	RSDELRR	745	RSDHLTK	950	DSDHLSR	1155	1000

358	GGCTGGGCG	541	RSDELRR	746	RSDHLTK	951	DSSHLSR	1156	225

361	GGGTTTGGG	542	RSDHLTR	747	QSSALTR	952	RSDHLTR	1157	130

363	GGGTTTGGG	543	RSDHLTR	748	QSSVLTR	953	RSDHLTR	1158	200

364	GTGTCCGAAG	544	RSDNLTR	749	DSAVLTT	954	RSDSLTR	1159	1000

365	GGTGCTGGT	545	QASHLTR	750	QASVLTR	955	QASHLTR	1160	600

366	GAGGGTGCT	546	QASVLTR	751	QASHLTR	956	RSDNLTR	1161	1000

367	GGGGGCGGG	547	RSDHLTR	752	DSGHLTR	957	RSDHLQR	1162	60

368	GAGGGGGCG	548	RSDELTR	753	RSDHLTR	958	RSDNLTR	1163	3.5

369	GTAGTTGTG	549	RSDALTR	754	TGGSLAR	959	QSGSLTR	1164	95

370	GTAGTTGTG	550	RSDALTR	755	NRATLAR	960	QSASLTR	1165	300

371	GTAGTTGTG	551	RSDALTR	756	NRATLAR	961	QSGSLTR	1166	175

372	GTAGTTGTG	552	RSDSLLR	757	TGGSLAR	962	QSASLTR	1167	112.5

373	GTAGTTGTG	553	RSDSLLR	758	NRATLAR	963	QSASLTR	1168	320

374	GCTGAGGAA	554	QRSNLVR	759	RSDNLTR	964	TSSELQR	1169	3.3

375	GAGGAAGAT	555	QQSNLAR	760	QSGNLQR	965	RSDNLTR	1170	85

377	GTGTTGGCAG	556	QSGSLTR	761	RGDALTS	966	RSDALTR	1171	89

378	GCCGAGGAGA	557	RSDNLTR	762	RSDNLTR	967	DRSSLTR	1172	31

379	GCCGAGGAGA	558	RSDNLTR	763	RSDNLTR	968	ERGTLAR	1173	3

380	GAGTCGCAAG	559	QSANLAR	764	RSDELTT	969	RSDNLAR	1174 1000

381	GCAGCTGCGC	560	RSDELTR	765	QSSDLQR	970	QSGDLTR	1175	1.5

383	TGGTTGGTAT	561	QSATLAR	766	RGDALTS	971	RSDHLTT	1176	1000

384	GTGGGCTTCA	562	DRSALTT	767	DRSHLAR	972	RSDALAR	1177	60

385	GGGGCGGAGC	563	RSDNLTR	768	RSDTLKK	973	RSDHLSR	1178	1.2

386	GGGGCGGAGC	564	RSDNLTR	769	RSDELQR	974	RSDHLSR	1179	0.4

387	GGCGAGGCAA	565	QSGSLTR	770	RSDNLAR	975	DRSHLAR	1180	2.5

388	GGCGAGGCAA	566	QSGDLTR	771	RSDNLAR	976	DRSHLAR	1181	28

390	GTGGCAGCGG	567	RSDTLKK	772	QSSDLQK	977	RSDALAR	1182	20

392	GTGGCAGCGG	568	RSDELTR	773	QSSDLQK	978	RSDALAR	1183	1000

396	GCGGGAGCAG	569	QSGSLTR	774	QSGHLQR	979	RSDTLKK	1184	18.8

397	GCGGGAGCAG	570	QSGDLTR	775	QSGHLQR	980	RSDTLKK	118	525

400	TCAGTGGTGG	571	RSDALAR	776	RSDSLAR	981	QSGDLRT	1186	40

405	GCGGCCGCA	572	RSDELTR	777	ERGTLAR	982	RSDERKR	1187	110

406	GCGGCCGCA	573	RSDELTR	778	DRSSLTR	983	RSDERKR	1188	110

407	GCGGCCGCA	574	QSWELTR	779	ERGTLAR	984	RSDERKR	1189	410

408	GCGGCCGCA	575	QSWELTR	780	DRSSLTR	985	RSDERKR	1190	380

409	GCGGCCGCA	576	QSGSLTR	781	ERGTLAR	986	RSDERKR	1191	50

410	GCAGAAGTC	577	RSDALTR	782	QSGNLTR	987	QSGSLTR	1192 3

411	GCGGCCGCA	578	QSGSLTR	783	RSDHLTT	988	RSDERKR	1193	1000

412	GCGTGGGCG	579	QSGSLTR	784	RSDHLTT	989	RSDERKR	1194	5

413	GCGTGGGCA	580	QSGSLTR	785	RSDHLTT	990	RSDERKR	1195	5

414	GCAGAAGCA	581	RSDELTR	786	QSANLQR	991	QSGSLTR	1196	1000

415	GTGTGCGGA	582	DRSHLTR	787	ERHSLQT	992	RSDALTR	1197	1000

416	TGTGCGGCC	583	ERGTLAR	788	RSDELRR	993	DRSHLQT	1198	1000

493	GGGGTGGCGG	584	RSDTLKK	789	RSDSLAR	994	RSDHLSR	1199	300

494	GCCGAGGAGA	585	RSDNLTR	790	RSDNLTR	995	DRSSLTR	1200	90

496	GGTGGTGGC	586	DTSHLRR	791	TSGHLQR	996	TSGHLSR	1201	1000

497	GTTTGCGTC	587	ETASLRR	792	DSAHLQR	997	TSSALSR	1202	1000

498	GAAGAGGCA	588	QTGELRR	793	RSDNLQR	998	QSGNLSR	1203	30

499	GCTTGTGAG	589	RTSNLRR	794	TSSHLQK	999	DTDHLRR	1204	1000

500	GCTTGTGAG	590	RSDNLTR	795	QSSNLQT	1000	DRSHLAR	1205	1000

501	GTGGGGGTT	591	NRATLAR	796	RSDHLSR	1001	RSDALAR	1206	8

502	GGGGTGGGA	592	QSAHLAR	797	RSDALAR	1002	RSDHLSR	1207	60

507	GAGGTAGAGG	593	RSDNLAR	798	QRSALAR	1003	RSDNLAR	1208	10

508	GAGGTAGAGG	594	RSDNLAR	799	QSATLR	1004	RSDNLAR	1209	10

509	GTCGTGTGGC	595	RSDHLTT	800	RSDALAR	1005	DRSALAR	1210	100

510	GTTGAGGAAG	596	QSGNLAR	801	RSDNLAR	1006	NRATLAR	1211	100

511	GTTGAGGAAG	597	QSGNLAR	802	RSDNLAR	1007	QSSALAR	1212	100

512	GAGGTGGAAG	598	QSGNLAR	803	RSDALAR	1008	RSDNLAR	1213	10

513	GAGGTGGAAG	599	QSANLAR	804	RSDALAR	1009	RSDNLAR	1214	1.5

514	TAGGTGGTGG	600	RSDALTR	805	RSDALAR	1010	RSDNLTT	1215	10

515	TGGGAGGAGT	601	RSDNLTR	806	RSDNLTR	1011	RSDHLTT	1216	0.5

516	GGAGGAGCT	602	TTSELRR	807	QSGHLQR	1012	QSGHLSR	1217	700

517	GGAGCTGGGG	603	RTDHLRR	808	TSSELQR	1013 QSGHLSR	1218	50

518	GGGGGAGGAG	604	QTGHLRR	809	QSGHLQR	1014	RSDHLSR	1219	30

519	GGGGAGGAGA	605	RSDNLAR	810	RSDNLSR	1015	RSDHLSR	1220	0.3

520	GGAGGAGAT	606	TTANLRR	811	QSGHLQR	1016	QSGHLSR	1221	300

521	GCAGCAGGA	607	QTGHLRR	812	QSGELQR	1017	QSGELSR	1222	1000

522	GATGAGGCA	608	QTGELRR	813	RSDNLQR	1018	TSANLSR	1223	200

527	GGGGAGGATC	609	TTSNLRR	814	RSSNLQR	1019	RSDHLSR	1224	2

528	GGGGAGGATC	610	TTSNLRR	815	RSSNLQR	1020	RSDHLSR	1225	10

529	GAGGCTTGGG	611	RTDHLRK	816	TSAELQR	1021	RSSNLSR	1226	1000

531	GCGGAGGCTT	612	TTGELRR	817	RSSNLQR	1022	RSDELSR	1227	160

532	GCGGAGGCTT	613	QSSDLQR	818	RSSNLQR	1023	RSDELSR	1228	100

533	GCGGAGGCTT	614	QSSDLQR	819	RSDNLAR	1024	RSADLSR	1229	7

534	GCGGAGGCTT	615	QSSDLQR	820	RSDNLAR	1025	RSDDLRR	1230	10

535	GCAGCCGGG	616	RTDHLRR	821	ESSDLQR	1026	QSGELSR	1231	1000

538	GCAGAGGCTT	617	QSSDLQR	822	RSDNLAR	1027	QSGSLTR	1232	70

540	TGGGCAGGCC	618	DRSHLTR	823	QSGSLTR	1028	RSDHLTT	1233	55

541	GGGGAGGAT	619	TTSNLRR	824	RSSNLQR	1029	RSDHLSR	1234	3

570	GGGGAAGGCT	620	DSGHLTR	825	QRSNLVR	1030	RSDHLTR	1235	20

571	GTGTGTGTGT	621	RSDSLTR	826	QRSNLVR	1031	RSDSLLR	1236	1000

572	GCATACGTGG	622	RSDSLLR	827	DKGNLQS	1032	QSDDLTR	1237	1000

573	GCATACGTG	623	RSDSLLR	828	DKGNLQS	1033	QSGDLTR	1238	1000

574	TACGTGGGGT	624	RSDHLTR	829	RSDHLTR	1034	DKGNLQT	1239	25

575	TACGTGGGCT	625	DFSHLTR	830	RSDHLTR	1035	DKGNLQT	1240	472

576	GAGGGTGTTG	626	NSDTLAR	831	TSGHLTR	1036	RSDNLTR	1241	200

577	GGAGCGGGGA	627	RSDHLSR	832	RSDELQR	1037	QSDHLTR	1242	200

579	GGGGTTGAGG	628	RSDNLTR	833	NRDTLAR	1038	TSGHLTR	1243	200

580	GGTGTTGGAG	629	QRAHLAR	834	NRDTLAR	1039	TSGHLTR	1244	1000

581	TACGTGGGTT	630	QSSHLTR	835	RSDSLLR	1040	DKGNLQT	1245	382

583	GTAGGGGTTG	631	NSSALTR	836	RSDHLTR	1041	QSASLTR	1246	46

584	GAAGGCGGAG	632	QAGHLTR	837	DKSHLTR	1042	QSGNLTR	1247	1000

585	GAAGGCGGAG	633	QAGHLTR	838	DSGHLTR	1043	QSGNLTR	1248	1000

587	GGGGGTTACG	634	DKGNLQT	839	TSGHLTR	1044	RSDHLSK	1249	500

588	GGGGGGGGGG	635	RSDHLSR	840	RSDHLTR	1045	RSDHLSK	1250	30

589	GGAGTATGCT	636	DSGHLAS	841	QSATLAR	1046	QSDHLTR	1251	1000

595	TGGTTGGTAT	637	QRGSLAR	842	RGDALTR	1047	RSDHLTT	1252	73.3

597	TGGTTGGTA	638	QNSAMRK	843	RGDALTS	1048	RSDHLTT	1253	1000

598	TGGTTGGTA	639	QRGSLAR	844	RDGSLTS	1049	RSDHLTT	1254	1000

599	TGGTTGGTA	640	QNSAMRK	845	RDGSLTS	1050	RSDHLTT	1255	1000

600	GAGTCGGAA	641	QSANLAR	846	RSDELRT	1051	RSDNLAR	1256	206.7

601	GAGTCGGAA	642	RSANLTR	847	RLDGLRT	1052	RSDNLAR	1257	606.7

602	GAGTCGGAA	643	RSANLTR	848	RQDTLVG	1053	RSDNLAR	1258	616.7

603	GAGTCGGAA	644	QSGNLAR	849	RSDELRT	1054	RSDNLAR	1259	166.7

606	GGGGAGGATC	645	TTSNLRR	850	RSDNLQR	1055	RSDHLSR	1260	0.2

[0117]

TABLE 3


		SEQ		SEQ		SEQ		SEQ	Kd
SBS#	TARGET	ID	F1	ID	F2	ID	F3	ID	(nM)

897	GAGGAGGTGA	1261	RSDALAR	1347	RSDNLAR	1433	RSDNLVR	1519	0.07

828	GCGGAGGACC	1262	EKANLTR	1348	RSDNLAR	1434	RSDERKR	1520	0.1

884	GAGGAGGTGA	1263	RSDSLTR	1349	RSDNLAR	1435	RSDNLVR	1521	0.15

817	GAGGAGGTGA	1264	RSDSLTR	1350	RSDNLAR	1436	RSDNLAR	1522	0.31

666	GCGGAGGCGC	1265	RSDDLTR	1351	RSDNLTR	1437	RSDTLKK	1523	0.5

829	GCGGAGGACC	1266	EKANLTR	1352	RSDNLAR	1438	RSDTLKK	1524	0.52

670	GACGTGGAGG	1267	RSDNLAR	1353	RSDALAR	1439	DRSNLTR	1525	0.57

801	AAGGAGTCGC	1268	RSADLRT	1354	RSDNLAR	1440	RSDNLTQ	1526	0.85

668	GTGGAGGCCA	1269	ERGTLAR	13S5	RSDNLAR	1441	RSDALAR	1527	1.13

895	ATGGATTCAG	1270	QSHDLTK	1356	TSGNLVR	1442	RSDALTQ	1528	1.4

799	GGGGGAGCTG	1271	QSSDLQR	1357	QRAHLER	1443	RSDHLSR	1529	1.85

798	GGGGGAGCTG	1272	QSSDLQR	1358	QSGHLER	1444	RSDHLSR	1530	3

842	GAGGTGGGCT	1273	DRSHLTR	1359	RSDALAR	1445	RSDNLAR	1531	5.4

894	TCAGTGGTAT	1274	QRSALAR	1360	RSDALSR	1446	QSHDLTK	1532	6.15

892	ATGGATTCAG	1275	QSHDLTK	1361	QQSNLVR	1447	RSDALTQ	1533	6.2

888	TCAGTGGTAT	1276	QSSSLVR	1362	RSDALSR	1448	QSHDLTK	1534	14

739	GCGGGCGGGC	1277	RSDHLTR	1363	ERGHLTR	1449	RSDDLRR	1535	16.5

850	CAGGCTGTGG	1278	RSDALTR	1364	QSSDLTR	1450	RSDNLRE	1536	17

797	GCAGAGGCTG	1279	QSSDLQR	1365	RSDNLAR	1451	QSGDLTR	1537	17.5

891	TCAGTGGTAT	1280	QSSSLVR	1366	RSDALSR	1452	QSGSLRT	1538	18.5

887	TCAGTGGTAT	1281	QRSALAR	1367	RSDALSR	1453	QSGDLRT	1539	23.75

672	TCGGACGTGG	1282	RSDALAR	1368	DRSNLTR	1454	RSDELRT	1540	24

836	GGGGAGGCCC	1283	ERGTLAR	1369	RSDNLAR	1455	RSDHLSR	1541	24.25

674	GCGGCGTCGG	1284	RSDELRT	1370	RADTLRR	1456	RSDTLKK	1542	27.5

849	GGGGCCCTGG	1285	RSDALRE	1371	DRSSLTR	1457	RSDHLTQ	1543	29.05

825	GAATGGGCAG	1286	QSGSLTR	1372	RSDHLTT	1458	QSGNLTR	1544	37.3

673	GCGGGTGTCT	1287	DRSALAR	1373	QSSHLAR	1459	RSDTLKK	1545	48.33

848	GGGGAGGCCC	1288	DRSSLTR	1374	RSDNLAR	1460	RSDHLSR	1546	49.5

662	AGAGCGGCAC	1289	QTGSLTR	1375	RSDELQR	1461	QSGHLNQ	1547	50

667	GAGTCGGACG	1290	DRSNLTR	1376	RSDELRT	1462	RSDNLAR	1548	50

803	GCAGCGGCTC	1291	QSSDLQR	1377	RSDELQR	1463	QSGSLTR	1549	57.5

671	TCGGACGAGT	1292	RSDNLAR	1378	DRSNLTR	1464	RSDELRT	1550	64

851	GAGATGGATC	1293	QSSNLQR	1379	RRDVLMN	1465	RLHNLQR	1551	74

804	GCAGCGGCTC	1294	QSSDLQR	1380	RSDDLNR	1466	QSGSLTR	1552	82.5

669	GACGAGTCGG	1295	RSDELRT	1381	RSDNLAR	1467	DRSNLTR	1553	90

682	GCTGCAGGAG	1296	RSDHLAR	1382	QSGDLTR	1468	QSSDLSR	1554	90

845	GAGATGGATC	1297	QSSNLQR	1383	RSDALRQ	1469	RLHNLQR	1S5S	112.5

663	AGAGCGGCAC	1298	QTGSLTR	1384	RSDELQR	1470	KNWKLQA	1556	115

738	GCGGGGTCCG	1299	ERGTLTT	1385	RSDHLSR	1471	RSDDLRR	1557	120

664	AGAGCGGCAC	1300	QTGSLTR	1386	RADTLRR	1472	ASSRLAT	1558	125

833	GACTAGGACC	1301	EKANLTR	1387	RSDNLTK	1473	DRSNLTR	1559	136

685	GCTGCAGGAG	1302	RSDHLAR	1388	QSGSLTR	1474	QSSDLSR	1560	150

835	TAGGGAGCGT	1303	RADTLRR	1389	QSGHLTR	1475	RSDNLTT	1561	150

847	TAGGGAGCGT	1304	RSDDLTR	1390	QSGHLTR	1476	RSDNLTT	1562	150

818	GAATGGGCAG	1305	QSGSLTR	1391	RSDHLTT	1477	QSSNLVR	1563	167

834	GACTAGGACC	1306	EKANLTR	1392	RSDHLTT	1478	DRSNLTR	1564	186

837	GGGGCCCTGG	1307	RSDALRE	1393	DRSSLTR	1479	RSDHLSR	1565	222

764	GCAGAGGCTG	1308	TSGELVR	1394	RSDNLAR	1480	QSGDLTR	1566	255

774	GCAGCGGTAG	1309	QRSALAR	1395	RSDELQR	1481	QSGDLTR	1567	258

765	GCCGAGGCCG	1310	ERGTLAR	1396	RSDNLAR	1482	ERGTLAR	1568	262.5

766	GCCGAGGCCG	1311	ERGTLAR	1397	RSDNLAR	1483	DRSDLTR	1569	262.5

775	GCAGCGGTAG	1312	QSGALTR	1398	RSDELQR	1484	QSGDLTR	1570	265

763	GCAGAGGCTG	1313	TSGELVR	1399	RSDNLAR	1485	QSGSLTR	1571	275

838	GGGGCCCTGG	1314	RSDALRE	1400	DRSSLTR	1486	RSDHLTA	1572	300

841	GAGTGTGAGG	1315	RSDNLAR	1401	QSSHLAS	1487	RSDNLAR	1573	300

770	TTGGCAGCCT	1316	DRSSLTR	1402	QSGSLTR	1488	RSDSLTK	1574	325

767	GGGGGAGCTG	1317	QSSDLAR	1403	QSGHLQR	1489	RSDHLSR	1575	335

800	TTGGCAGCCT	1318	ERGTLAR	1404	QSGSLTR	1490	RSDSLTK	1576	400

832	GACTAGGACC	1319	EKANLTR	1405	RSDNLTT	1491	DRSNLTR	1577	408

844	GAGATGGATC	1320	QSSNLQR	1406	RSDALRQ	1492	RSDNLQR	1578	444

683	GCTGCAGGAG	1321	QSGHLAR	1407	QSGSLTR	1493	QSSDLSR	1579	500

805	GCAGCGGTAG	1322	QRSALAR	1408	RSDELQR	1494	QSGSLTR	1580	500

839	GAGTGTGAGG	1323	RSDNLAR	1409	TSDHLAS	1495	RSDNLAR	1581	625

840	GAGTGTGAGG	1324	RSDNLAR	1410	MSHHLKT	1496	RSDNLAR	1582	625

830	GGAGAGTCGG	1325	RSDELRT	1411	RSDNLAR	1497	QRAHLAR	1583	683

831	GGAGAGTCGG	1326	RSDDLTK	1412	RSDNLAR	1498	QRAHLAR	1584	700

684	GCTGCAGGAG	1327	RSAHLAR	1413	QSGSLTR	1499	QSSDLSR	1585	850

846	GAGATGGATC	1328	QSSNLQR	1414	RRDVLMN	1500	RSDNLQR	1586	889.5

819	AAGTAGGGTG	1329	QSSHLTR	1415	RSDNLTT	1501	RSDNLTQ	1587	1000

820	ACGGTAGTTA	1330	QSSALTR	1416	QRSALAR	1502	RSDTLTQ	1588	1000

821	ACGGTAGTTA	1331	NRATLAR	1417	QRSALAR	1503	RSDTLTQ	1589	1000

822	GTGTGCTGGT	1332	RSDHLTT	1418	ERQHLAT	1504	RSDALAR	1590	1000

823	GTGTGCTGGT	1333	RSDHLTK	1419	ERQHLAT	1505	RSDALAR	1591	1000

824	GTGTGCTGGT	1334	RSDHLTT	1420	DRSHLRT	1506	RSDALAR	1592	1000

885	GTGTGCTGGT	1335	RSDHLTK	1421	DRSHLRT	1507	RSDALAR	1593	1000

886	TCAGTGGTAT	1336	QSSSLVR	1422	RSDALSR	1508	QSGDLRT	1594	1000

889	ATGGATTCAG	1337	QSGSLTT	1423	QQSNLVR	1509	RSDALTQ	1595	1000

890	CTGGTATGTC	1338	QRSHLTT	1424	QRSALAR	1510	RSDALRE	1596	1000

896	AAGTAGGGTG	1339	TSGHLVR	1425	RSDNLTT	1511	RSDNLTQ	1597	1000

898	ACGGTAGTTA	1340	NRATLAR	1426	QSSSLVR	1512	RSDTLTQ	1598	1000

899	CTGGTATGTC	1341	QRSHLTT	1427	QSSSLVR	1513	RSDALRE	1599	1000

900	CTGGTATGTC	1342	MSHHLKE	1428	QSSSLVR	1514	RSDALRE	1600	1000

901	CTGGTATGTC	1343	MSHHLKE	1429	QRSALAR	1515	RSDALRE	1601	1000

773	GCAGCGGTAG	1344	QSQALTR	1430	RSDELQR	1516	QSGSLTR	1602	1250

768	GGGGGAGCTG	1345	QSSDLAR	1431	QRAHLER	1517	RSDHLSR	1603	2000

681	GCTGCAGGAG	1346	RSAHLAR	1432	QSGDLTR	1518	QSSDLSR	1604	3000

[0118]

TABLE 4


		SEQ	F1	SEQ	F2	SEQ	F3	SEQ	Kd
SBS#	TARGET	ID		ID		ID		ID	(nM)

607	AAGGTGGCAG	1605	QSGDLTR	1707	RSDSLAR	1809	RLDNRTA	1911	6.5

608	TTGGCTGGGC	1606	GSWHLTR	1708	QSSDLQR	1810	RSDSLTK	1912	8

611	GTGGCTGCAG	1607	QSGDLTR	1709	QSSDLQR	1811	RSDALAR	1913	11.5

612	GTGGCTGCAG	1608	QSGTLTR	1710	QSSDLQR	1812	RSDALAR	1914	0.38

613	TTGGCTGGGC	1609	RSDHLAR	1711	QSSDLQR	1813	RGDALTS	1915	1.45

614	TTGGCTGGGC	1610	RSDHLAR	1712	QSSDLQR	1814	RSDSLTK	1916	2

616	GAGGAGGATG	1611	QSSNLQR	1713	RSDNLAR	1815	RSDNLQR	1917	0.08

617	AAGGGGGGG	1612	RSDHLSR	1714	RSDHLTR	1816	RKDNMTA	1918	1

618	AAGGGGGGG	1613	RSDHLSR	1715	RSDHLTR	1817	RKDNMTQ	1919	0.55

619	AAGGGGGGG	1614	RSDHLSR	1716	RSDHLTR	1818	RKDNMTN	1920	1.34

620	AAGGGGGGG	1615	RSDHLSR	1717	RSDHLTR	1819	RLDNRTA	1921	0.54

621	AAGGGGGGG	1616	RSDHLSR	1718	RSDHLTR	1820	RLDNRTQ	1922	0.75

624	ACGGATGTCT	1617	DRSALAR	1719	TSANLAR	1821	RSDTLRS	1923	7

628	TTGTAGGGGA	1618	RSDHLTR	1720	RSDNLTT	1822	RGDALTS	1924	130

629	TTGTAGGGGA	1619	RSSHLTR	1721	RSDNLTT	1823	RGDALTS	1925	150

630	CGGGGAGAGT	1620	RSDNLAR	1722	QSGHLQR	1824	RSDHLRE	1926	37.5

646	TTGGTGGAAG	1621	QSGNLAR	1723	RSDALAR	1825	RGDALTS	1927	35

647	TTGGTGGAAG	1622	QSANLAR	1724	RSDALAR	1826	RGDALTS	1928	40

651	GTTGTGGAAT	1623	QSGNLSR	1725	RSDALAR	1827	NRATLAR	1929	67.5

652	TAGGAGGCTG	1624	QSSDLQR	1726	RSDNLAR	1828	RSDNLTT	1930	1.5

653	TAGGAGGCTG	1625	TTSDLTR	1727	RSDNLAR	1829	RSDNLTT	1931	5.5

654	TAGGCATAAA	1626	QSGNLRT	1728	QSGSLTR	1830	RSDNLTT	1932	105

655	TAGGCATAAA	1627	QSGNLRT	1729	QSSTLRR	1831	RSDNLTT	1933	1000

656	TAGGCATAAA	1628	QSGNLRT	1730	QSGSLTR	1832	RSDNLTS	1934	540

657	TAGGCATAAA	1629	QSGNLRT	1731	QSSTLRR	1833	RSDNLTS	1935	300

660	GAGGGAGTTC	1630	NRATLAR	1732	QSGHLTR	1834	RSDNLAR	1936	8.25

661	GAGGGAGTTC	1631	TTSALTR	1733	QSGHLTR	1835	RSDNLAR	1937	1.73

665	GCGGAGGCGC	1632	RSDDVTR	1734	RSDNLTR	1836	RSDDLRR	1938	12.5

689	AAGGCGGAGA	1633	RSDNLTR	1735	RSDELQR	1837	RLDNRTA	1939	82.5

692	AAGGCGGAGA	1634	RSDNLTR	1736	RSDELQR	1838	RSDNLTQ	1940	51

693	AAGGCGGAGA	1635	RSDNLTR	1737	RADTLRR	1839	RLDNRTA	1941	95

694	AAGGCGGAGA	1636	RSDNLTR	1738	RADTLRR	1840	RSDNLTQ	1942	28.5

695	GGGGGCGAGC	1637	RSSNLTR	1739	DRSHLAR	1841	RSDHLTR	1943	850

697	TGAGCGGCGG	1638	RSDELTR	1740	RSDELSR	1842	QSGHLTK	1944	200

698	TGAGCGGCGG	1639	RSDELTR	1741	RSDELSR	1843	QSHGLTS	1945	300

699	GCGGCGGCAG	1640	QSGSLTR	1742	RSDDLQR	1844	RSDERKR	1946	21.5

700	GCGGCGGCAG	1641	QSGDLTR	1743	RSDDLQR	1845	RSDERKR	1947	45

701	GCAGCGGAGC	1642	RSDNLAR	1744	RSDELQR	1846	QSGSLTR	1948	50.5

702	GCAGCGGAGC	1643	RSDNLAR	1745	RSDELQR	1847	QSGDLTR	1949	73.5

704	AAGGTGGCAG	1644	QSGDLTR	1746	RSDSLAR	1848	RSDNLTQ	1950	5

705	GGGGTGGGGC	1645	RSDHLAR	1747	RSDSLAR	1849	RSDHLSR	1951	0.01

706	GGGGTGGGGC	1646	RSDHLAR	1748	RSDSLLR	1850	RSDHLSR	1952	0.05

708	GAGTCGGAA	1647	QSANLAR	1749	RQDTLVG	1851	RSDNLAR	1953	300

709	GAGTCGGAA	1648	QSANLAR	1750	RKDVLVS	1852	RSDNLAR	1954	400

710	GAGTCGGAA	1649	QSGNLAR	1751	RLDGLRT	1853	RSDNLAR	1955	400

711	GAGTCGGAA	1650	QSGNLAR	1752	RQDTLVG	1854	RSDNLAR	1956	400

712	GGTGAGGAGT	1651	RSDNLAR	1753	RSDNLAR	1855	MSDHLSR	1957	9.5

713	GGTGAGGAGT	1652	RSDNLAR	1754	RSDNLAR	1856	MSHHLSR	1958	0.15

714	TGGGTCGCGG	1653	RSDELRR	1755	DRSALAR	1857	RSDHLTT	1959	200

715	TGGGTCGCGG	1654	RADTLRR	1756	DRSALAR	1858	RSDHLTT	1960	0.46

716	TTGGGAGCAC	1655	QSGSLTR	1757	QSGHLQR	1859	RGDALTS	1961	200

717	TTGGGAGCAC	1656	QSGSLTR	1758	QSGHLQR	1860	RSDALTK	1962	150

718	TTGGGAGCAC	1657	QSGSLTR	1759	QSGHLQR	1861	RSDALTR	1963	107.5

719	GGCATGGTGG	1658	RSDALTR	1760	RSDALTS	1862	DRSHLAR	1964	20

720	GAAGAGGATG	1659	TTSNLAR	1761	RSDNLAR	1863	QSGNLTR	1965	1.6

722	ATGGGGGTGG	1660	RSDALTR	1762	RSDHLTR	1864	RSDALRQ	1966	0.7

724	GGCATGGTGG	1661	RSDALTR	1763	RSDALRQ	1865	DRSHLAR	1967	2.5

725	GCTTGAGTTA	1662	QSSALAR	1764	QSGHLQK	1866	QSSDLQR	1968	3000

726	GAAGAGGATG	1663	QSSNLAR	1765	RSDNLAR	1867	QSGNLTR	1969	1.5

727	GCGGTGGCTC	1664	QSSDLTR	1766	RSDALSR	1868	RSDTLKK	1970	0.1

728	GGTGAGGAGT	1665	RSDNLAR	1767	RSDNLAR	1869	DSSKLSR	1971	15

729	GGAGGGGAGT	1666	RSDNLAR	1768	RSDHLSR	1870	QSGHLAR	1972	1000

730	TGGGTCGCGG	1667	RSDDLTR	1769	DRSALAR	1871	RSDHLTT	1973	1000

731	GTGGGGGAGA	1668	RSDNLAR	1770	RSDHLSR	1872	RSDALAR	1974	12

732	GCGGGTGGGG	1669	RSDHLAR	1771	QSSHLAR	1873	RSDDLTR	1975	22.5

733	GCGGGTGGGG	1670	RSDHLAR	1772	QSSHLAR	1874	RSDTLKK	1976	0.32

734	GGGGCTGGGT	1671	RSDHLAR	1773	QSSDLSR	1875	RSDHLSR	1977	0.25

735	GCGGTGGCTC	1672	QSSDLTR	1774	RSDALSR	1876	RSDERKR	1978	0.05

736	GAGGTGGGGA	1673	RSDHLAR	1775	RSDALSR	1877	RSDNLSR	1979	0.47

737	GGAGGGGAGT	1674	RSDNLAR	1776	RSDHLSR	1878	QRGHLSR	1980	1000

740	AAGGTGGCAG	1675	QSGSLTR	1777	RSDALAR	1879	RSDNRTA	1981	12.5

741	AAGGCTGAGA	1676	RSDNLTR	1778	QSSDLQR	1880	RSDNLTQ	1982	15

742	ACGGGGTTAT	1677	QRGALAS	1779	RSDHLSR	1881	RSDTLKQ	1983	29

743	ACGGGGTTAT	1678	QRGALAS	1780	RSDHLSR	1882	RSDTLTQ	1984	10

744	ACGGGGTTAT	1679	QRSALAS	1781	RSDHLSR	1883	RSDTLKQ	1985	8.33

745	ACGGGGTTAT	1680	QRSALAS	1782	RSDHLSR	1884	RSDTLTQ	1986	12.5

746	CTGGAAGCAT	1681	QSGSLTR	1783	QSGNLAR	1885	RSDALRE	1987	2.07

747	CTATTTTGGG	1682	RSDHLTT	1784	QSSALRT	1886	QSGALRE	1988	2000

748	TTGGACGGCG	1683	DSGHLTR	1785	DRSNLER	1887	RGDALTS	1989	112.3

749	TTGGACGGCG	1684	DRSHLTR	1786	DSSNLTR	1888	RGDALTS	1990	11.33

750	GAGGGAGCGA	1685	RSDELTR	1787	QSAHLAR	1889	RSDNLAR	1991	52

751	GGTGAGGAGT	1686	RSDNLAR	1788	RSDNLAR	1890	NRSHTAR	1992	7

752	GAGGTGGGGA	1687	RSHHLAR	1789	RSDALSR	1891	RSDNLSR	1993	31

757	CGGGCGGCTG	1688	QSSDLRR	1790	RSDELQR	1892	RSDHLRE	1994	14.5

758	CGGGCGGCTG	1689	QSSDLRR	1791	RADTLRR	1893	RSDHLRE	1995	16.5

759	TTGGACGGCG	1690	DSGHLTR	1792	DSSNLTR	1894	RGDALTS	1996	37

760	TTGGACGGCG	1691	DRSHLTR	1793	DRSNLER	1895	RGDALTS	1997	148.5

761	GCGGTGGCTC	1692	QSSDLQR	1794	RSDALSR	1896	RSDERKR	1998	6

762	GCGGTGGCTC	1693	QSSDLQR	1795	RSDALSR	1897	RSDTLKK	1999	18

776	ATGGACGGGT	1694	RSDHLAR	1796	DRSNLER	1898	RSDSLNQ	2000	0.4

777	ATGGACGGGT	1695	RSDHLAR	1797	DRSNLTR	1899	RSDALSA	2001	3.4

779	CGGGGAGCAG	1696	QSGSLTR	1798	QSGHLTR	1900	RSDHLAE	2002	0.5

780	CGGGGAGCAG	1697	QSGSLTR	1799	QSGHLTR	1901	RSDHLRA	2003	0.5

781	GGGGAGCAGC	1698	RSSNLRE	1800	RSDNLAR	1902	RSDHLTR	2004	4.25

783	TTGGGAGCGG	1699	RSDELTR	1801	QSGHLQR	1903	RGDALTS	2005	2000

785	TTGGGAGCGG	1700	RSDTLKK	1802	QSGHLQR	1904	RSDALTS	2006	50

786	TTGGGAGCGG	1701	RSDTLKK	1803	QSGHLQR	1905	RGDALRS	2007	2000

787	AGGGAGGATG	1702	QSDNLAR	1804	RSDNLAR	1906	RSDHLTQ	2008	4

826	GAGGGAGCGA	1703	RSDELTR	1805	QSGHLAR	1907	RSDNLAR	2009	2.75

827	GAGGGAGCGA	1704	RADTLRR	1806	QSGHLAR	1908	RSDNLAR	2010	1.2

882	GCGTGGGCGT	1705	RSDELTR	1807	RSDHLTT	1909	RSDERKR	2011	0.01

883	GCGTGGGCGT	1706	RSDELTR 1808	RSDHLTT	1910	RSDERKR	2012	1

[0119]

TABLE 5


		SEQ		SEQ		SEQ		SEQ	Kd
SBS#	TARGET	ID	F1	ID	F2	ID	F3	ID	(nM)

903	ATGGAAGGG	2013	RSDHLAR	2513	QSGNLAR	3013	RSDALRQ	3513	1.027

904	AAGGGTGAC	2014	DSSNLTR	2514	QSSHLAR	3014	RSDNLTQ	3514	1

905	GTGGTGGTG	2015	RSSALTR	2515	RSDSLAR	3015	RSDSLAR	3515	1.15

908	AAGGTCTCA	2016	QSGDLRT	2516	DRSALAR	3016	RSDNLRQ	3516	50

909	GTGGAAGAA	2017	QSGNLSR	2517	QSGNLQR	3017	RSDALAR	3517	16.4

910	ATGGAAGAT	2018	QSSNLAR	2518	QSGNLQR	3018	RSDALAQ	3518	0.03

911	ATGGGTGCA	2019	QSGSLTR	2519	QSSHLAR	3019	RSDALAQ	3519	0.91

912	TCAGAGGTG	2020	RSDSLAR	2520	RSDNLTR	3020	QSGDLRT	3520	0.135

914	CAGGAAAAG	2021	RSDNLTQ	2521	QSGNLAR	3021	RSDNLRE	3521	1.26

915	CAGGAAAAG	2022	RSDNLRQ	2522	QSGNLAR	3022	RSDNLRE	3522	45.15

916	GAGGAAGGA	2023	QSGHLAR	2523	QSGNLAR	3023	RSDNLQR	3523	1.3

919	TCATAGTAG	2024	RSDNLTT	2524	RSDNLRT	3024	QSGDLRT	3524	250

920	GATGTGGTA	2025	QSSSLVR	2525	RSDSLAR	3025	TSANLSR	3525	4

921	AAGGTCTCA	2026	QSGDLRT	2526	DPGALVR	3026	RSDNLRQ	3526	11

922	AAGGTCTCA	2027	QSHDLTK	2527	DRSALAR	3027	RSDNLRQ	3527	4

923	AAGGTCTCA	2028	QSHDLTK	2528	DPGALVR	3028	RSDNLRQ	3528	2

926	GTGGTGGTG	2029	RSDALTR	2529	RSDSLAR	3029	RSDSLAR	3529	7.502

927	CAGGTTGAG	2030	RSDNLAR	2530	TSGSLTR	3030	RSDNLRE	3530	3.61

928	CAGGTTGAG	2031	RSDNLAR	2531	QSSALTR	3031	RSDNLRE	3531	25

929	CAGGTAGAT	2032	QSSNLAR	2532	QSATLAR	3032	RSDNLRE	3532	1.3

931	GAGGAAGAG	2033	RSDNLAR	2533	QSSNLVR	3033	RSDNLAR	3533	2

932	ATGGAAGGG	2034	RSDHLAR	2534	QSSNLVR	3034	RSDALRQ	3534	797

933	GACGAGGAA	2035	QSANLAR	2535	RSDNLAR	3035	DRSNLTR	3535	500

934	ATGGAAGAT	2036	QSSNLAR	2536	QSGNLQR	3036	RSDALTS	3536	0.07

935	ATGGGTGCA	2037	QSGSLTR	2537	QSSHLAR	3037	RSDALTS	3537	0.91

937	GTGGGGGCT	2038	QSSDLTR	2538	RSDHLTR	3038	RSDSLAR	3538	0.03

938	GTGGGGGCT	2039	QSSDLRR	2539	RSDHLTR	3039	RSDSLAR	3539	0.049

939	GGGGGCTGG	2040	RSDHLTT	2540	DRSHLAR	3040	RSDHLSK	3540	0.352

940	GGGGGCTGG	2041	RSDHLTK	2541	DRSHLAR	3041	RSDHLSK	3541	1.5

941	GGGGCTGGG	2042	RSDHLAR	2542	QSSDLRR	3042	RSDKLSR	3542	0.077

942	GGGGCTGGG	2043	RSDHLAR	2543	QSSDLRR	3043	RSDHLSK	3543	0.13

943	GGGGCTGGG	2044	RSDHLAR	2544	TSGELVR	3044	RSDKLSR	3544	0.067

944	GGGGCTGGG	2045	RSDHLAR	2545	TSGELVR	3045	RSDHLSK	3545	0.027

945	GGTGCGGTG	2046	RSDSLTR	2546	RADTLRR	3046	MSHHLSR	3546	0.027

946	GGTGCGGTG	2047	RSDSLTR	2547	RSDVLQR	3047	MSHHLSR	3547	0.027

947	GGTGCGGTG	2048	RSDSLTR	2548	RSDELQR	3048	QSSHLAR	3548	0.013

948	GGTGCGGTG	2049	RSDSLTR	2549	RSDVLQR	3049	QSSHLAR	3549	0.017

962	GAGGCGGCA	2050	QSGSLTR	2550	RSDELQR	3050	RSDNLAR	3550	0.015

963	GAGGCGGCA	2051	QSGSLTR	2551	RSDDLQR	3051	RSDNLAR	3551	0.015

964	GCGGCGGTG	2052	RSDALAR	2552	RSDELQR	3050	RSDERKR	3552 0.041

965	GCGGCGGCC	2053	ERGDLTR	2553	RSDELQR	3053	RSDERKR	3553	3.1

966	GAGGAGGCC	2054	ERGTLAR	2554	RSDNLSR	3054	RSDNLAR	3554	0.028

967	GAGGAGGCC	2055	DRSSLTR	2555	RSDNLSR	3055	RSDNLAR	3555	0.055

968	GAGGCCGCA	2056	QSGSLTR	2556	DRSSLTR	3056	RSDNLAR	3556	1.4

969	GAGGCCGCA	2057	QSGSLTR	2557	DRSDLTR	3057	RSDNLAR	3557	0.275

970	GTGGGCGCC	2058	ERGTLAR	2558	DRSHLAR	3058	RSDALAR	3558	1.859

971	GTGGGCGCC	2059	DRSSLTR	2559	DRSHLAR	3059	RSDALAR	3559	0.144

972	GTGGGCGCC	2060	ERGDLTR	2560	DRSHLAR	3060	RSDALAR	3560	1.748

973	GCCGCGGTC	2061	DRSALTR	2561	RSDELQR	3061	ERGTLAR	3561	0.6

974	GCCGCGGTC	2062	DRSALTR	2562	RSDELQR	3062	DRSDLTR	3562	0.038

975	CAGGCCGCT	2063	QSSDLTR	2563	DRSSLTR	3063	RSDNLRE	3563	1.1

976	CAGGCCGCT	2064	QSSDLTR	2564	DRSDLTR	3064	RSDNLRE	3564	4.12

977	CTGGCAGTG	2065	RSDSLTR	2565	QSGSLTR	3065	RSDALRE	3565	0.017

978	CTGGCAGTG	2066	RSDSLTR	2566	QSGDLTR	3066	RSDALRE	3566	1.576

979	CTGGCGGCG	2067	RSSDLTR	2567	RSDELQR	3067	RSDALRE	3567	1.59

980	CTGGCGGCG	2068	RSDDLTR	2568	RSDELQR	3068	RSDALRE	3568	2.2

981	CAGGCGGCG	2069	RSDDLTR	2569	RSDELQR	3069	RSDNLRE	3569	0.375

982	CCGGGCTGG	2070	RSDHLTT	2570	DRSHLAR	3070	RSDELRE	3570	0.03

983	CCGGGCTGG	2071	RSDHLTK	2571	DRSHLAR	3071	RSDELRE	3571	1.385

984	GACGGCGAG	2072	RSDNLAR	2572	DRSHLAR	3072	DRSNLTR	3572	1.6

985	GACGGCGAG	2073	RSDNLAR	2573	DRSHLAR	3073	EKANLTR	3573	0.965

986	GGTGCTGAT	2074	QSSNLQR	2574	QSSDLQR	3074	MSHHLSR	3574	1.6

987	GGTGCTGAT	2075	QSSNLQR	2575	QSSDLQR	3075	TSGHLVR	3575	33.55

988	GGTGCTGAT	2076	TSGNLVR	2576	QSSDLQR	3076	MSHHLSR	3576	0.15

989	GGTGAGGGG	2077	RSDHLAR	2577	RSDNLAR	3077	MSHHLSR	3577	1.9

990	AAGGTGGGC	2078	DRSHLTR	2578	RSDSLAR	3078	RSDNLTQ	3578	5.35

991	AAGGTGGGC	2079	DRSHLTR	2579	SSGSLVR	3079	RSDNLTQ	3579	0.06

993	GGGGCTGGG	2080	RSDHLAR	2580	TSGELVR	3080	RSDHLSR	3580	3.1

994	GGGGGCTGG	2081	RSDHLTK	2581	DRSHLAR	3081	RSDHLSR	3581	0.03

995	GGGGAGGAA	2082	QSANLAR	2582	RSDNLAR	3082	RSDHLSK	3582	0.08

996	CAGTTGGTC	2083	DRSALAR	2583	RSDALTS	3083	RSDNLRE	3583	9.6

997	AGAGAGGCT	2084	QSSDLTR	2584	RSDNLAR	3084	QSGHLNQ	584	1.65

998	ACGTAGTAG	2085	RSANLRT	2585	RSDNLTK	3085	RSDTLKQ	3585	0.23

999	AGAGAGGCT	2086	QSSDLTR	2586	RSDNLAR	3086	QSGKLTQ	3586	0.6

1000	CAGTTGGTC	2087	DRSALAR	2587	RSDALTR	3087	RSDNLRE	3587	11.15

1001	GGAGCTGAC	2088	EKANLTR	2588	QSSDLSR	3088	QRAHLAR	3588	1.8

1002	GCGGAGGAG	2089	RSDNLVR	2589	RSDNLAR	3089	RSDERKR	3589	0.028

1003	ACGTAGTAG	2090	RSANLRT	2590	RSDNLTK	3090	RSDTLRS	3590	0.118

1004	ACGTAGTAG	2091	RSDNLTT	2591	RSDNLTK	3091	RSDTLRS	3591	1.4

1006	GTAGGGGCG	2092	RSDDLTR	2592	RSDHLTR	3092	QRASLTR	3592	0.898

1007	GAGAGAGAT	2093	QSSNLQR	2593	QSGHLTR	3093	RLHNLAR	3593	167

1008	GAGATGGAG	2094	RSDNLSR	2594	RSDSLTQ	3094	RLHNLAR	3594	0.4

1009	GAGATGGAG	2095	RSDNLSR	2595	RSDSLTQ	3095	RSDNLSR	3595	1.9

1010	GAGAGAGAT	2096	QSSNLQR	2596	QSGHLTR	3096	RSDNLAR	3596	8.2

1011	TTGGTGGCG	2097	RSADLTR	2597	RSDSLAR	3097	RSDSLTK	3597	0.03

1012	GACGTAGGG	2098	RSDHLTR	2598	QSSSLVR	3098	DRSNLTR	3598	0.032

1013	GAGAGAGAT	2099	QSSNLQR	2599	QSGHLNQ	3099	RSDNLAR	3599	0.15

1014	GACGTAGGG	2100	RSDHLTR	2600	QSGSLTR	3100	DRSNLTR	3600	0.01

1015	GCGGAGGAG	2101	RSDNLVR	2601	RSDNLAR	3101	RSDTLKK	3601	0.008

1016	CAGTTGGTC	2102	DRSALAR	2602	RSDSLTK	3102	RSDNLRE	3602	0.09

1017	CTGGATGAC	2103	EKANLTR	2603	TSGNLVR	3103	RSDALRE	3603	0.233

1018	GTAGTAGAA	2104	QSANLAR	2604	QSSSLVR	3104	QRASLAR	3604	7.2

1019	AGGGAGGAG	2105	RSDNLAR	2605	RSDNLAR	3105	RSDHLTQ	3605	0.022

1020	ACGTAGTAG	2106	RSDNLTT	2606	RSDNLTK	3106	RSDTLKQ	3606	0.69

1022	GAGGAGGTG	2107	RSDALAR	2607	RSDNLAR	3107	RSDNLAR	3607	0.01

1024	GGGGAGGAA	2108	QSANLAR	2608	RSDNLAR	3108	RSDHLSR	3608	0.08

1025	GAGGAGGTG	2109	QSSALTR	2609	QSSSLVR	3109	RSDTLTQ	3609	0.115

1026	GTGGCTTGT	2110	MSHHLKE	2610	QSSDLSR	3110	RSDALAR	3610	0.076

1027	GCGGCGGTG	2111	RSDALAR	2611	RSDELQR	3111	RSDELQR	3611	0.054

1032	GGTGCTGAT	2112	TSGNLVR	2612	QSSDLQR	3112	TSGHLVR	3612	0.52

1033	GTGTTCGTG	2113	RSDALAR	2613	DRSALTT	3113	RSDALAR	3613	685.2

1034	GTGTTCGTG	2114	RSDALAR	2614	DRSALTK	3114	RSDALAR	3614	14.55

1035	GTGTTCGTG	2115	RSDALAR	2615	DRSALRT	3115	RSDALAR	3615	56

1037	GTAGGGGCA	2116	QSGSLTR	2616	RSDHLSR	3116	QRASLAR	3616	0.05

1038	GTAGGGGCA	2117	QTGELRR	2617	RSDHLSR	3117	QRASLAR	3617	0.152

1039	GGGGCTGGG	2118	RSDHLSR	2618	TSGELVR	3118	RSDHLTR	3618	1.37

1040	GGGGCTGGG	2119	RSDHLSR	2619	QSSDLQR	3119	RSDHLSK	3619	0.05

1041	TCATAGTAG	2120	RSDNLTT	2620	RSDNLRT	3120	QSHDLTK	3620	2.06

1043	CAGGGAGAG	2121	RSDNLAR	2621	QSGHLTR	3121	RSDNLRE	3621	0.16

1044	CAGGGAGAG	2122	RSDNLAR	2622	QRAHLER	3122	RSDNLRE	3622	1.07

1045	GGGGCAGGA	2123	QSGHLAR	2623	QSGSLTR	3123	RSDHLSR	3623	0.15

1046	GGGGCAGGA	2124	QSGHLAR	2624	QSGDLRR	3124	RSDHLSR	3624	0.09

1047	GGGGCAGGA	2125	QRAHLER	2625	QSGSLTR	3125	RSDHLSR	3625	24.7

1048	CAGGCTGTA	2126	QSGALTR	2626	QSSDLQR	3126	RSDNLRE	3626	1.387

1049	CAGGCTGTA	2127	QRASLAR	2627	QSSDLQR	3127	RSDNLRE	3627	55.6

1050	CAGGCTGTA	2128	QSSSLVR	2628	QSSDLQR	3128	RSDNLRE	3628	0.125

1051	GAGGCTGAG	2129	RSDNLTR	2629	QSSDLQR	3129	RSDNLVR	3629	0.02

1052	TAGGACGGG	2130	RSDHLAR	2630	EKANLTR	3130	RSDNLTT	3630	0.28

1053	TAGGACGGG	2131	RSDHLAR	2631	DRSNLTR	3131	RSDNLTT	3631	0.025

1054	GCTGCAGGG	2132	RSDHLAR	2632	QSGSLTR	3132	QSSDLQR	3632	0.033

1055	GCTGCAGGG	2133	RSDHLAR	2633	QSGSLTR	3133	TSGDLTR	3633	18.73

1056	GCTGCAGGG	2134	RSDHLAR	2634	QSGSLTR	3134	QSSDLQR	3634	0.045

1057	GCTGCAGGG	2135	RSDHLAR	2635	QSGDLTR	3135	TSGDLTR	3635	0.483

1058	GGGGCCGCG	2136	RSDELTR	2636	DRSSLTR	3136	RSDHLSR	3636	6.277

1059	GGGGCCGCG	2137	RSDELTR	2637	DRSDLTR	3137	RSDHLSR	3637	0.152

1060	GCGGAGGCC	2138	ERGTLAR	2638	RSDNLAR	3138	RSDERKR	3638	0.69

1061	GTTGCGGGG	2139	RSDHLAR	2639	RSDELQR	3139	QSSALTR	3639	0.165

1062	GTTGCGGGG	2140	RSDHLAR	2640	RSDELQR	3140	TSGSLTR	3640	0.068

1063	GTTGCGGGG	2141	RSDHLAR	2641	RSDELQR	3141	MSHALSR	3641	0.96

1064	GCGGCAGTG	2142	RSDALTR	2642	QSGSLTR	3142	RSDERKR	3642	0.453

1065	TGGGGCGGG	2143	RSDHLAR	2643	DRSHLAR	3143	RSDHLTT	3643	1.37

1066	GAGGGCGGT	2144	QSSHLTR	2644	DRSHLAR	3144	RSDNLVR	3644	0.15

1067	GAGGGCGGT	2145	TSGHLVR	2645	DRSHLAR	3145	RSDNLVR	3645	1.37

1068	GCAGGGGGC	2146	DRSHLTR	2646	RSDHLTR	3146	QSGDLTR	3646	2.05

1069	GCAGGCGGT	2147	DRSHLTR	2647	RSDHLTR	3147	QSGSLTR	3647	0.1

1070	GGGGCAGGC	2148	DRSHLTR	2648	QSGSLTR	3148	RSDHLSR	3648	0.456

1071	GGGGCAGGC	2149	DRSHLTR	2649	QSGDLTR	3149	RSDHLSR	3649	0.2

1072	GGATTGGCT	2150	QSSDLTR	2650	RSDALTT	3150	QRAHLAR	3650	0.46

1073	GGATTGGCT	2151	QSSDLTR	2651	RSDALTK	3151	QRAHLAR	3651	1.37

1075	GTGTTGGCG	2152	RSDELTR	2652	RSDALTK	3152	RSDALTR	3652	0.915

1076	GCGGCAGCG	2153	RSDELTR	2653	QSGSLTR	3153	RSDERKR	3653	4.1

1077	GCGGCAGCG	2154	RSDELTR	2654	QSGDLRR	3154	RSDERKR	3654	6.2

1078	GGGGGGGCC	2155	ERGTLAR	2655	RSDHLSR	3155	RSDHLSR	3655	0.2

1079	GGGGGGGCC	2156	ERGDLTR	2656	RSDHLSR	3156	RSDHLSR	3656	4.1

1080	CTGGAGGCG	2157	RSDELTR	2657	RSDNLAR	3157	RSDALRE	3657	1.37

1081	GGGGAGGTG	2158	RSDALTR	2658	RSDNLTR	3158	RSDHLSR	3658	0.05

1082	CTGGCGGCG	2159	RSDELTR	2659	RSDELTR	3159	RSDALRE	3659	0.152

1083	CTGGTGGCA	2160	QSGDLTR	2660	RSDALSR	3160	RSDALRE	3660	0.152

1084	GGTGAGGCG	2161	RSDELTR	2661	RSDNLAR	3161	MSHHLSR	3661	0.5

1085	GGTGAGGCG	2162	RSDELTR	2662	RSDNLAR	3162	QSSHLAR	3662	0.46

1086	GGGGCTGGG	2163	RSDHLSR	2663	QSSDLQR	3163	RSDHLTR	3663	0.1

1087	CGGGCGGCC	2164	ERGDLTR	2664	RSDELQR	3164	RSDHLAE	3664	1.24

1088	CGGGCGGCC	2165	ERGDLTR	2665	RSDELQR	3165	RSDHLRE	3665	0.905

1089	GACGAGGCT	2166	QSSDLRR	2666	RSDNLAR	3166	DRSNLTR	3666	0.171

1090	AAGGCGCTG	2167	RSDALRE	2667	RSDELQR	3167	RSDNLTQ	3667	30.3

1091	GTAGAGGAC	2168	DRSNLTR	2668	RSDNLAR	3168	QRASLAR	3668	0.085

1092	GCCTTGGCT	2169	QSSDLRR	2669	RGDALTS	3169	DRSDLTR	3669	2.735

1093	GCGGAGTCG	2170	RSADLRT	2670	RSDNLAR	3170	RSDERKR	3670	0.046

1094	GCGGTTGGT	2171	TSGHLVR	2671	QSSALTR	3171	RSDERKR	3671	12.34

1095	GGGGGAGCC	2172	ERGDLTR	2672	QRAHLER	3172	RSDHLSR	3672	0.395

1096	GGGGGAGCC	2173	DRSSLTR	2673	QRAHLER	3173	RSDHLSR	3673	0.019

1097	GAGGCCGAA	2174	QSANLAR	2674	DCRDLAR	3174	RSDNLAR	3674	0.77

1098	GCCGGGGAG	2175	RSDNLTR	2675	RSDHLTR	3175	DRSDLTR	3675	0.055

1099	GCGGAGTCG	2176	TSGHLVR	2676	TSGSLTR	3176	RSDERKR	3676	0.45

1100	GTGTTGGTA	2177	QSGALTR	2677	RGDALTS	3177	RSDALTR	3677	1.4

1101	ATGGGAGTT	2178	TTSALTR	2678	QPAHLER	3178	RSDALRQ	3678	0.065

1102	AAGGCAGAA	2179	QSANLAR	2679	QSGSLTR	3179	RSDNLTQ	3679	8.15

1103	AAGGCAGAA	2180	QSANLAR	2680	QSGDLTR	3180	RSDNLTQ	3680	1.4

1104	CGGGCAGCT	2181	QSSDLRR	2681	QSGSLTR	3181	RSDHLRE	3681	0.08

1105	CTGGCAGCC	2182	ERGDLTR	2682	QSGDLTR	3182	RSDALRE	3682	2.45

1106	CTGGCAGCC	2183	DRSSLTR	2683	QSGDLTR	3183	RSDALRE	3683	0.19

1107	GCGGGAGTT	2184	QSSALAR	2684	QRAHLER	3184	RSDERKR	3684	0.06

1108	CAGGCTGGA	2185	QSGHLAR	2685	TSGELVR	3185	RSDNLRE	3685	0.007

1109	AGGGGAGCC	2186	ERGDLTR	2686	QRAHLER	3186	RSDHLTQ	3686	0.347

1110	AGGGGAGCC	2187	DRSSLTR	2687	QRAHLER	3187	RSDHLTQ	3687	0.095

1111	CTGGTAGGG	2188	RSDHLAR	2688	QSSSLVR	3188	RSDALRE	3688	0.095

1112	CTGGTAGGG	2189	RSDHLAR	2689	QSATLAR	3189	RSDALRE	3689	0.125

1113	CTGGGGGCA	2190	QSGDLTR	2690	RSDHLTR	3190	RSDALRE	3690	0.06

1114	CAGGTTGAT	2191	QSSNLAR	2691	TSGSLTR	3191	RSDNLRE	3691	2.75

1115	CAGGTTGAT	2192	QSSNLAR	2692	QSSALTR	3192	RSDNLRE	3692	0.7

1116	CCGGAAGCG	2193	RSDELTR	2693	QSSNLVR	3193	RSDELRE	3693	12.3

1117	GCAGCGCAG	2194	RSSNLRE	2694	RSDELTR	3194	QSGSLTR	3694	2.85

1118	TAGGGAGTC	2195	DRSALTR	2695	QRAHLER	3195	RSDNLTT	3695	1.4

1119	TGGGAGGGT	2196	TSGHLVR	2696	RSDNLAR	3196	RSDHLTT	3696	0.1

1120	AGGGACGCG	2197	RSDELTR	2697	DRSNLTR	3197	RSDHLTQ	3697	2.735

1121	CTGGTGGCC	2198	ERGDLTR	2698	RSDALTR	3198	RSDALRE	3698	2.76

1122	CTGGTGGCC	2199	DRSSLTR	2699	RSDALTR	3199	RSDALRE	3699	0.101

1123	TAGGAAGCA	2200	QSGSLTR	2700	QSGNLAR	3200	RSDNLTT	3700	0.065

1124	GTGGATGGA	2201	QSGHLAR	2701	TSGNLVR	3201	RSDALTR	3701	0.101

1126	TTGGCTATG	2202	RSDALTS	2702	TSGELVR	3202	RGDALTS	3702	0.46

1127	CAGGGGGTT	2203	QSSALAR	2703	RSDHLTR	3203	RSDNLRE	3703	0.1

1128	AAGGTCGCC	2204	ERGDLTR	2704	DPGALVR	3204	RSDNLTQ	3704	5.45

1130	GGTGCAGAC	2205	DRSNLTR	2705	QSGDLTR	3205	MSHHLSR	3705	0.1

1131	GTGGGAGCC	2206	ERGDLTR	2706	QRAHLER	3206	RSDALTR	3706	0.95

1132	GGGGCTGGA	2207	QSGHLAR	2707	TSGELVR	3207	RSDHLSR	3707	0.055

1133	GGGGCTGGA	2208	QRAHLER	2708	TSGELVR	3208	RSDHLSR	3708	0.5

1134	TGGGGGTGG	2209	RSDHLTT	2709	RSDHLTR	3209	RSDHLTT	3709	0.067

1135	GCGGCGGGG	2210	RSDHLAR	2710	RSDELQR	3210	RSDERKR	3710	0.025

1136	CCGGGAGTG	2211	RSDALTR	2711	QRAHLER	3211	RSDTLRE	3711	0.225

1137	CCGGGAGTG	2212	RSSALTR	2712	QRAHLER	3212	RSDTLRE	3712	0.085

1138	CAGGGGGTA	2213	QSGALTR	2713	RSDHLTR	3213	RSDNLRE	3713	0.027

1139	ACGGCCGAG	2214	RSDNLAR	2714	DRSDLTR	3214	RSDTLTQ	3714	0.535

1140	AAGGGTGCG	2215	RSDELTR	2715	QSSHLAR	3215	RSDNLTQ	3715	0.3

1141	ATGGACTTG	2216	RGDALTS	2716	DRSNLTR	3216	RSDALTQ	3716	1.7

1148	TTGGAGGAG	2217	RSDNLTR	2717	RSDNLTR	3217	RGDALTS	3717	0.006

1149	TTGGAGGAG	2218	RSDNLTR	2718	RSDNLTR	3218	RSDALTK	3718	0.004

1150	GAAGAGGCA	2219	QSGSLTR	2719	RSDNLTR	3219	QSGNLTR	3719	0.004

1151	GTAGTATGG	2220	RSDHLTT	2720	QRSALAR	3220	QRASLAR	3720	1.63

1152	AAGGCTGGA	2221	QSGHLAR	2721	TSGELVR	3221	RSDNLTQ	3721	1.605

1153	AAGGCTGGA	2222	QRAHLAR	2722	TSGELVR	3222	RSDNLTQ	3722	8.2

1154	CTGGCGTAG	2223	RSDNLTT	2723	RSDELQR	3223	RSDALRE	3723	1.04

1156	ATGGTTGAA	2224	QSANLAR	2724	QSSALTR	3224	RSDALRQ	3724	7.2

1157	ATGGTTGAA	2225	QSANLAR	2725	TSGSLTR	3225	RSDALRQ	3725	0.885

1158	AGGGGAGAA	2226	QSANLAR	2726	QSGHLTR	3226	RSDHLTQ	3726	0.1

1159	AGGGGAGAA	2227	QSANLAR	2727	QRAHLER	3227	RSDHLTQ	3727	0.555

1160	TGGGAAGGC	2228	DRSHLAR	2728	QSSNLVR	3228	RSDHLTT	3728	0.415

1161	GAGGCCGGC	2229	DRSHLAR	2729	DRSDLTR	3229	RSDNLAR	3729	0.45

1162	GTGTTGGTA	2230	QSGALTR	2730	RADALMV	3230	RSDALTR	3730	0.465

1163	GTGTGAGCC	2231	ERGDLTR	2731	QSGHLTT	3231	RSDALTR	3731	1.45

1164	GTGTGAGCC	2232	ERGDLTR	2732	QSVHLQS	3232	RSDALTR	3732	15.4

1165	GCGAAGGTG	2233	RSDALTR	2733	RSDNLTQ	3233	RSDERKR	3733	1.4

1166	GCGAAGGTG	2234	RSDALTR	2734	RSDNLTQ	3234	RSSDRKR	3734	0.195

1167	GCGAAGGTG	2235	RSDALTR	2735	RSDNLTQ	3235	RSHDRKR	3735	0.95

1168	AAGGCGCTG	2236	RSDALRE	2736	RSSDLTR	3236	RSDNLTQ	3736	2.8

1169	GTAGAGGAC	2237	DRSNLTR	2737	RSDNLAR	3237	QSSSLVR	3737	0.053

1170	GCCTTGGCT	2238	QSSDLRR	2738	RADALMV	3238	DRSDLTR	3738	2.75

1171	GCGGAGTCG	2239	RSDDLRT	2739	RSDNLAR	3239	RSDERKR	3739	0.18

1172	GCCGGGGAG	2240	RSDNLTR	2740	RSDHLTR	3240	ERGDLTR	3740	0.01

1173	GCTGAAGGG	2241	RSDHLSR	2741	QSGNLAR	3241	QSSDLRR	3741	0.008

1174	GCTGAAGGG	2242	RSDHLSR	2742	QSSNLVR	3242	QSSDLRR	3742	0.018

1175	AAGGTCGCC	2243	DRSDLTR	2743	DPGALVR	3243	RSDNLTQ	3743	8.9

1176	GTGGGAGCC	2244	DRSDLTR	2744	QPAHLER	3244	RSDALTR	3744	4.1

1177	CCGGGCGCA	2245	QSGSLTR	2745	DRSHLAR	3245	RSDTLRE	3745	4.1

1178	GAGGATGGC	2246	DRSHLAR	2746	TSGNLVR	3246	RSDNLAR	3746	0.085

1179	GCAGCGCAG	2247	RSSNLRE	2747	RSSDLTR	3247	QSGSLTR	3747	2.735

1180	AAGGAAAGA	2248	QSGHLNQ	2748	QSGNLAR	3248	RSDNLTQ	3748	4.825

1181	TTGGCTATG	2249	RSDALRQ	2749	TSGELVR	3249	RGDALTS	3749	8.2

1182	CAGGAAGGC	2250	DRSHLAR	2750	QSGNLAR	3250	RSDNLRE	3750	1.48

1183	CAGGAAGGC	2251	DRSHLAR	2751	QSSNLVR	3251	RSDNLRE	3751	1.935

1184	AAGGAAAGA	2252	KNWKLQA	2752	QSGNLAR	3252	RSDNLTQ	3752	2.785

1185	AAGGAAAGA	2253	KNWKLQA	2753	QSHNLAR	3253	RSDNLTQ	3753	5.25

1186	GCCGAGGTG	2254	RSDSLLR	2754	RSKNLQR	3254	ERGTLAR	3754	27.5

1187	CTGGTGGGC	2255	DRSHLAR	2755	RSDALTR	3255	RSDALRE	3755	0.006

1188	GTAGTATGG	2256	RSDHLTT	2756	QSSSLVR	3256	QRASLAR	3756	2.74

1189	ATGGTTGAA	2257	QSANLAR	2757	TSGALTR	3257	RSDALRQ	3757	1.51

1190	ATGGCAGTG	2258	RSDALTR	2758	QSGDLTR	3258	RSDSLNQ	3758	1.484

1191	ATGGCAGTG	2259	RSDALTR	2759	QSGSLTR	3259	RSDSLNQ	3759	5.325

1192	ATGGCAGTG	2260	RSDALTR	2760	QSGDLTR	3260	RSDALTQ	3760	2.364

1193	ATGGCAGTG	2261	RSDALTR	2761	QSGSLTR	3261	RSDALTQ	3761	3.125

1194	GAGAAGGTG	2262	RSDALTR	2762	RSDNRTA	3262	RSDNLTR	3762	2.19

1195	GAGAAGGTG	2263	RSDALTR	2763	RSDNRTA	3263	RSSNLTR	3763	2.8

1197	GAAGGTGCC	2264	ERGDLTR	2764	MSHHLSR	3264	QSGNLTR	3764	14.8

1199	ATGGAGAAG	2265	RSDNRTA	2765	RSDNLTR	3265	RSDALTQ	3765	3.428

1200	ATGGAGAAG	2266	RSDNRTA	2766	RSSNLTR	3266	RSDALTQ	3766	16.87

1201	ATGGAGAAG	2267	RSDNRTA	2767	RSHNLTR	3267	RSDALTQ	3767	14.8

1202	CTGGAGTAC	2268	DRSNLRT	2768	RSDNLTR	3268	RSDALRE	3768	2.834

1203	GGAGTACTG	2269	RSDALRE	2769	QRSALAR	3269	QRAHLAR	3769	2.945

1204	GGAGTACTG	2270	RSDALRE	2770	QSSSLVR	3270	QRAHLAR	3770	4.38

1205	CGGGCAGCT	2271	QSSDLRR	2771	QSGDLTR	3271	RSDHLRE	3771	0.9

1206	GCGGGAGTT	2272	TTSALTR	2772	QRAHLER	3272	RSDERKR	3772	0.034

1207	CAGGCTGGA	2273	QRAHLER	2773	TSGELVR	3273	RSDNLRE	3773	0.45

1209	CCGGAAGCG	2274	RSDELTR	2774	QSSNLVR	3274	RSDTLRE	3774	19.28

1211	GCAGCGCAG	2275	RSDNLRE	2775	RSDELTR	3275	QSGSLTR	3775	6.5

1212	CAGGGGGTT	2276	TTSALTR	2776	RSDHLTR	3276	RSDNLRE	3776	0.05

1213	GAAGAAGAG	2277	RSDNLTR	2777	QSSNLVR	3277	QSGNLTR	3777	12.3

1214	ATGGGAGTT	2278	TTSALTR	2778	QRAHLER	3278	RSDALTQ	3778	0.46

1215	GTGGGGGCT	2279	QSSDLRR	2779	RSDHLTR	3279	RSDALTR	3779	0.003

1217	GAAGAGGCA	2280	QSGSLTR	2780	RSDNLTR	3280	QSANLTR	3780	0.004

1218	GCGGTGAGG	2281	RSDHLTQ	2781	RSQALTR	3281	RSDERKR	3781	0.46

1219	AAGGAAAGG	2282	RSDHLTQ	2782	QSHNLAR	3282	RSDNLTQ	3782	0.68

1220	AAGGAAAGG	2283	RSDHLTQ	2783	QSGNLAR	3283	RSDNLTQ	3783	0.175

1221	AAGGAAAGG	2284	RSDHLTQ	2784	QSSNLVR	3284	RSDNLTQ	3784	1.4

1222	CAGGAGGGC	2285	DRSHLAR	2785	RSDNLAR	3285	RSDNLRE	3785	0.155

1223	ATGGACTTG	2286	RSDALTK	2786	DRSNLTR	3286	RSDALTQ	3786	7

1224	ATGGACTTG	2287	RADALMV	2787	DRSNLTR	3287	RSDALTQ	3787	12

1227	GAATAGGGG	2288	RSDHLSR	2788	RSDHLTK	3288	QSGNLAR	3788	25

1228	ACGGCCGAG	2289	RSDNLAR	2789	DRSDLTR	3289	RSDDLTQ	3789	12

1229	AAGGGTGCG	2290	RSDELTR	2790	MSHHLSR	3290	RSDNLTQ	3790	8.2

1230	AAGGGAGAC	2291	DRSNLTR	2791	QSGHLTR	3291	RSDNLTQ	3791	0.383

1231	AAGGGAGAC	2292	DRSNLTR	2792	QRAHLER	3292	RSDNLTQ	3792	0.213

1232	TGGGACCTG	2293	RSDALRE	2793	DRSNLTR	3293	RSDHLTT	3793	0.113

1233	TGGGACCTG	2294	RSDALRE	2794	DRSNLTR	3294	RSDHLTT	3794	0.635

1234	GAGTAGGCA	2295	QSGSLTR	2795	RSDNLTK	3295	RSDNLAR	3795	0.101

1236	GAGTAGGCA	2296	QSGSLTR	2796	RSDHLTT	3296	RSDNLAR	3796	0.065

1237	GAAGGAGAG	2297	RSDNLAR	2797	QRAHLER	3297	QSGNLAR	3797	0.065

1238	CTGGATGTT	2298	QSSALAR	2798	TSGNLVR	3298	RSDALRE	3798	0.313

1239	CAGGACGTG	2299	RSDALTR	2799	DPGNLVR	3299	RSDNLKD	3799	0.144

1240	GGGGAGGCA	2300	QSGSLTR	2800	RSDNLTR	3300	RSDHLSR	3800	0.056

1241	GAGGTGTCA	2301	QSHDLTK	2801	RSDALAR	3301	RSDNLAR	3801	0.027

1242	GGGGTTGAA	2302	QSANLAR	2802	TSGSLTR	3302	RSDHLSR	3802	0.02

1243	GGGGTTGAA	2303	QSANLAR	2803	QSSALTR	3303	RSDHLSR	3803	0.101

1244	GTCGCGGTG	2304	RSDALTR	2804	RSDELQR	3304	DRSALAR	3804	0.044

1245	GTCGCGGTG	2305	RSDALTR	2805	RSDELQR	3305	DSGSLTR	3805	0.102

1246	GTGGTTGCG	2306	RSDELTR	2806	TSGSLTR	3306	RSDALTR	3806	0.051

1247	GTGGTTGCG	2307	RSDELTR	2807	TSGALTR	3307	RSDALTR	3807	0.117

1248	GTCTAGGTA	2308	QSGALTR	2808	RSDNLTT	3308	DRSALAR	3808 5.14

1249	CCGGGAGCG	2309	RSDELTR	2809	QSGHLTR	3309	RSDTLRE	3809	0.26

1250	GAAGGAGAG	2310	RSDNLAR	2810	QSGHLTR	3310	QSGNLAR	3810	0.31

1252	CCGGCTGGA	2311	QRAHLER	2811	QSSDLTR	3311	RSDTLRE	3811	0.153

1253	CCGGGAGCG	2312	RSDELTR	2812	QRAHLER	3312	RSDTLRE	3812	0.228

1255	ACGTAGTAG	2313	RSDNLTT	2813	RSDNLTK	3313	RSDTLKQ	3813	0.69

1256	GGGGAGGAT	2314	QSSNLAR	2814	RSDNLQR	3314	RSDHLSR	3814	2

1257	GGGGAGGAT	2315	TTSNLAR	2815	RSDNLQR	3315	RSDHLSR	3815	1

1258	GGGGAGGAT	2316	QSSNLRR	2816	RSDNLQR	3316	RSDHLSR	3816	2

1259	GAGTGTGTG	2317	RSDSLLR	2817	DRDHLTR	3317	RSDNLAR	3817	1.5

1260	GAGTGTGTG	2318	RLDSLLR	2818	DRDHLTR	3318	RSDNLAR	3818	1.8

1261	TGCGGGGCA	2319	QSGDLTR	2819	RSDHLTR	3319	RRDTLHR	3819	0.2

1262	TGCGGGGCA	2320	QSGDLTR	2820	RSDHLTR	3320	RLDTLGR	3820	3

1263	TGCGGGGCA	2321	QSGDLTR	2821	RSDHLTR	3321	DSGHLAS	3821	21

1264	AAGTTGGTT	2322	TTSALTR	2822	RADALMV	3322	RSDNLTQ	3822	0.21

1265	AAGTTGGTT	2323	TTSALTR	2823	RSDALTT	3323	RSDNLTQ	3823	0.077

1266	CAGGGTGGC	2324	DRSHLTR	2824	QSSHLAR	3324	RSDNLRE	3824	6.1

1267	TAGGCAGTC	2325	DRSALTR	2825	QSGSLTR	3325	RSDNLTT	3825	6

1268	CTGTTGGCT	2326	QSSDLTR	2826	RAEDLMV	3326	RSDALRE	3826	1.52

1269	CTGTTGGCT	2327	QSSDLTR	2827	RSDALTT	3327	RSDALRE	3827	12.3

1270	TTGGATGGA	2328	QSGHLAR	2828	TSGNLVR	3328	RSDALTK	3828	0.4

1271	GTGGCACTG	2329	RSDALRE	2829	QSGSLTR	3329	RSDALTR	3829	0.915

1272	CAGGAGTCC	2330	DRSSLTT	2830	RSDNLAR	3330	RSDNLRE	3830	0.04

1273	CAGGAGTCC	2331	ERGDLTT	2831	RSDNLAR	3331	RSDNLRE	3831	0.1

1274	GCATGGGAA	2332	QSANLSR	2832	RSDHLTT	3332	QSGSLTR	3832	0.306

1275	GCATGGGAA	2333	QRSNLVR	2833	RSDHLTT	3333	QSGSLTR	3833	0.326

1276	TAGGAAGAG	2334	RSDNLAR	2834	QRSNLVR	3334	RSDNLTT	3834	0.685

1277	GAAGAGGGG	2335	RSDHLAR	2835	RSDNLAR	3335	QSGNLTR	3835	0.421

1278	GAGTAGGCA	2336	QSGSLTR	2836	RSDNLRT	3336	RSDNLAR	3836	0.019

1279	GAGGTGTCA	2337	QSGDLRT	2837	RSDALAR	3337	RSDNLAR	3837	0.025

1282	TCGGTCGCC	2338	ERGDLTR	2838	DPGALVR	3338	RSDELRT	3838	74.1

1287	GTGGTAGGA	2339	QSGHLAR	2839	QSGALAR	3339	RSDALTR	3839	0.152

1288	CAGGGTGGC	2340	DRSHLTR	2840	QSSHLAR	3340	RSDNLTE	3840	4.1

1289	TAGGCAGTC	2341	DRSALTR	2841	QSGSLTR	3341	RSDNLTK	3841	1.37

1290	GTGGTGATA	2342	QSGALTQ	2842	RSHALTR	3342	RSDALTR	3842	24.05

1291	GTGGTGATA	2343	QQASLNA	2843	RSHALTR	3343	RSDALTR	3843	20.55

1292	TTGGATGGA	2344	QSGHLAR	2844	TSGNLVR	3344	RSDALTT	3844	4.12

1293	AAGGTAGGT	2345	TSGHLVR	2845	QSGALAR	3345	RSDNLTQ	3845	0.457

1294	AAGGTAGGT	2346	MSHHLSR	2846	QSGALAR	3346	RSDNLTQ	3846	2.75

1295	CAGGAGTCC	2347	DRSSLTT	2847	RSDNLAR	3347	RSDNLTE	3847	0.116

1296	CAGGAGTCC	2348	ERGDLTT	2848	RSDNLAR	3348	RSDNLTE	3848	37

1297	TAGGAAGAG	2349	RSDNLAR	2849	QRSNLVR	3349	RSDNLTK	3849	0.05

1298	CAGGACGTG	2350	RSDLATR	2850	DPGNLVR	3350	RSDNLTE	3850	0.05

1300	GTCTAGGTA	2351	QSGALTR	2851	RSDNLTK	3351	DRSALAR	3851	0.46

1302	CCGGCTGGA	2352	QSGHLTR	2852	QSSDLTR	3352	RSDTLRE	3852	0.05

1303	TAGGAGTTT	2353	QRSALAS	2853	RSDNLAR	3353	RSDNLTT	3853	0.088

1306	CTGGCCTTG	2354	RSDALTT	2854	DCRDLAR	3354	RSDALRE	3854	2.285

1308	TGGGCAGCC	2355	ERGTLAR	2855	QSGSLTR	3355	RSDHLTT	3855	0.305

1309	TAGGAGTTT	2356	QSSALAS	2856	RSDNLAR	3356	RSDNLTT	3856	0.184

1310	TAGGAGTTT	2357	TTSALAS	2857	RSDNLAR	3357	RSDNLTT	3857	0.075

1311	TGGGCAGCC	2358	ERGDLAR	2858	QSGSLTR	3358	RSDHLTT	3858	0.91

1312	GGGGCGTGA	2359	QSGHLTK	2859	RSDELQR	3359	RSDHLSR	3859	0.23

1313	GGGGCGTGA	2360	QSGHLTT	2860	RSDELQR	3360	RSDHLSR	3860	0.09

1314	GTACAGTAG	2361	RSDNLTT	2861	RSDNLRE	3361	QSSSLVR	3861	3.09

1315	GTACAGTAG	2362	RSDNLTT	2862	RSDNLTE	3362	QSSSLVR	3862	9.27

1318	ATGGTGTGT	2363	TSSHLAS	2863	RSDALAR	3363	RSDALAQ	3863	0.048

1319	ATGGTGTGT	2364	MSHHLTT	2864	RSDALAR	3364	RSDALAQ	3864	0.228

1320	TTGGGAGAG	2365	RSDNLAR	2865	QRAHLER	3365	RSDALTT	3865	0.044

1321	TTGGGAGAG	2366	RSDNLAR	2866	QRAHLER	3366	RADALMV	3866	0.127

1322	GTGGGAATA	2367	QSGALTQ	2867	QSGHLTR	3367	RSDALTR	3867	0.799

1323	GTGGGAATA	2368	QLTGLNQ	2868	QSGHLTR	3368	RSDALTR	3868	0.744

1324	GTGGGAATA	2369	QQASLNA	2869	QSHHLTR	3369	RSDALTR	3869	18.52

1325	TTGGTTGGT	2370	TSGHLVR	2870	TSGSLTR	3370	RSDALTK	3870	0.306

1326	TTGGTTGGT	2371	TSGHLVR	2871	QSSALTR	3371	RSDALTK	3871	4.385

1327	TTGGTTGGT	2372	TSGHLVR	2872	TSGSLTR	3372	RSDALTT	3872	0.566

1328	TTGGTTGGT	2373	TSGHLVR	2873	QSSALTR	3373	RSDALTT	3873	7.95

1329	CTGGCCTGG	2374	RSDHLTT	2874	DRSDLTR	3374	RSDALRE	3874	0.68

1330	GAGGTGTGA	2375	QSGHLTT	2875	RSDALTR	3375	RSDNLAR	3875	0.175

1331	CTGGCCTGG	2376	RSDHLTT	2876	DCRDLAR	3376	RSDALRE	3876	0.388

1334	CCGGCGCTG	2377	RSDALRE	2877	RSSDLTR	3377	RSDDLRE	3877	0.31

1335	GACGCTGGC	2378	DRSHLTR	2878	QSSDLTR	3378	DSSNLTR	3878	1.4

1336	CGGGCTGGA	2379	QSGHLAR	2879	QSSDLTR	3379	RSDHLAE	3879	1.4

1337	CGGGCTGGA	2380	QSSHLAR	2880	QSSDLTR	3380	RSDHLAE	3880	0.235

1338	GGGATGGCG	2381	RSDELTR	2881	RSDALTQ	3381	RSDHLSR	3881	1.04

1339	GGGATGGCG	2382	RSDELTR	2882	RSDSLTQ	3382	RSDHLSR	3882	0.569

1340	GGGATGGCG	2383	RSDELTR	2883	RSDALTQ	3383	RSHHLSR	3883	0.751

1341	GGGATGGCG	2384	RSDELTR	2884	RSDSLTQ	3384	RSHHLSR	3884	4.1

1342	CAGGCGCAG	2385	RSDNLRE	2885	RSSDLTR	3385	RSDNLTE	3885	0.68

1343	CAGGCGCAG	2386	RSDNLTT	2886	RTSTLTR	3386	RSDNLTE	3886	37.04

1344	CCGGGCGAC	2387	DRSNLTR	2887	DRSHLAR	3387	RSDTLRE	3887	2.28

1346	GATGTGTGA	2388	QSGHLTT	2888	RSDALAR	3388	TSANLSR	3888	0.153

1347	CAGTGAATG	2389	RSDALTS	2889	QSHHLTT	3389	RSDNLTE	3889	8.23

1348	GGGTCACTG	2390	RSDALTA	2890	QAATLTT	3390	RSDHLSR	3890	2.58

1350	CAGTGAATG	2391	RSDALTQ	2891	QSGHLTT	3391	RSDNLTE	3891	74.1

1351	GGGTCACTG	2392	RSDALRE	2892	QSHDLTK	3392	RSDHLSR	3892	0.234

1352	GTGTGGGTC	2393	DRSALAR	2893	RSDHLTT	3393	RSDALTR	3893	0.023

1353	CTGGCGAGA	2394	QSGHLNQ	2894	RSDELQR	3394	RSDALRE	3894	56.53

1354	CTGGCGAGA	2395	KNWKLQA	2895	RSDELQR	3395	RSDALRE	3895	20.85

1355	GCTTTGGCA	2396	QSGSLTR	2896	RSDALTT	3396	QSSDLTR	3896	0.172

1356	GCTTTGGCA	2397	QSGSLTR	2897	RADALMV	3397	QSSDLTR	3897	0.034

1357	GACTTGGTA	2398	QSSSLVR	2898	RSDALTT	3398	DRSNLTR	3898	0.032

1358	GACTTGGTA	2399	QSSSLVR	2899	RADALMV	3399	DRSNLTR	3899	0.05

1360	CAGTTGTGA	2400	QSGHLTT	2900	RADALMV	3400	RSDNLTE	3900	41.7

1361	AAGGAAAAA	2401	QKTNLDT	2901	QSGNLQR	3401	RSDNLTQ	3901	0.835

1362	AAGGAAAAA	2402	QSGNLNQ	2902	QSGNLQR	3402	RSDNLTQ	3902	0.332

1363	AAGGAAAAA	2403	QKTNLDT	2903	QRSNLVR	3403	RSDNLTQ	3903	74.1

1364	ATGGGTGAA	2404	QSANLSR	2904	QSSHLAR	3404	RSDALAQ	3904	1.22

1365	ATGGGTGAA	2405	QRSNLVR	2905	QSSLLAR	3405	RSDALAQ	3905	0.152

1366	ATGGGTGAA	2406	QSANLSR	2906	TSGHLVR	3406	RSDALAQ	3906	22.63

1367	ATGGGTGAA	2407	QRSNLVR	2907	TSGHLVR	3407	RSDALAQ	3907	1.028

1368	CTGGGAGAT	2408	QSSNLAR	2908	QRAHLER	3408	RSDALRE	3908	0.051

1369	CTGGGAGAT	2409	QSSNLAR	2909	QSGHLTR	3409	RSDALRE	3909	0.227

1373	GTGGTGGGC	2410	DRSHLTR	2910	RSDALSR	3410	RSDALTR	3910	0.025

1374	CCGGCGGTG	2411	RSDALTR	2911	RSDELQR	3411	RSDELRE	3911	0.003

1375	CCGGCGGTG	2412	RSDALTR	2912	RSDDLQR	3412	RSDELRE	3912	0.008

1376	CCGGCGGTG	2413	RSDALTR	2913	RSDERKR	3413	RSDELRE	3913	0.858

1377	CCGGCGGTG	2414	RSDALTR	2914	RSDELQR	3414	RSDDLRE	3914	0.012

1378	CCGGCGGTG	2415	RSDALTR	2915	RSDDLQR	3415	RSDDLRE	3915	0.012

1379	CCGGCGGTG	2416	RSDALTR	2916	RSDERKR	3416	RSDDLRE	3916	0.25

1380	GCCGACGGT	2417	QSSHLTR	2917	DRSNLTR	3417	ERGDLTR	3917	0.076

1381	GCCGACGGT	2418	QSSHLTR	2918	DPGNLVR	3418	ERGDLTR	3918	0.23

1382	GCCGACGGT	2419	QSSHLTR	2919	DRSNLTR	3419	DCRDLAR	3919	3.1

1383	GCCGACGGT	2420	QSSHLTR	2920	DPGNLVR	3420	DCRDLAR	3920	1.74

1384	GGTGTGGGC	2421	DRSHLTR	2921	RSDALSR	3421	MSHHLSR	3921	0.013

1385	TGGGCAAGA	2422	QSGHLNQ	2922	QSGSLTR	3422	RSDHLTT	3922	0.229

1386	TGGGCAAGA	2423	ENWKLQA	2923	QSGSLTR	3423	RSDHLTT	3923	0.193

1389	CTGGCCTGG	2424	RSDHLTT	2924	DCRDLAR	3424	RSDALRE	3924	0.175

1393	TGGGAAGCT	2425	QSSDLRR	2925	QSGNLAR	3425	RSDHLTT	3925	0.1

1394	TGGGAAGCT	2426	QSSDLRR	2926	QSGNLAR	3426	RSDHLTK	3926	0.04

1395	GAAGAGGGA	2427	QSGHLQR	2927	RSDNLAR	3427	QSGNLAR	3927	0.025

1396	GAAGAGGGA	2428	QRAHLAR	2928	RSDNLAR	3428	QSGNLAR	3928	0.107

1397	GAAGAGGGA	2429	QSSHLAR	2929	RSDNLAR	3429	QSGNLAR	3929	0.14

1398	TAATGGGGG	2430	RSDHLSR	2930	RSDHLTT	3430	QSGNLRT	3930	0.065

1399	TGGGAGTGT	2431	TKQHLKT	2931	RSDNLAR	3431	RSDHLTT	3931	0.1

1400	CCGGGTGAG	2432	RSDNLAR	2932	QSSHLAR	3432	RSDDLRE	3932	0.371

1401	GAGTTGGCC	2433	ERGTLAR	2933	RADALMV	3433	RSDNLAR	3933	0.167

1402	CTGGAGTTG	2434	RGDALTS	2934	RSDNLAR	3434	RSDALRE	3934	0.15

1403	ATGGCAATG	2435	RSDALTQ	2935	QSGSLTR	3435	RSDALTQ	3935	0.07

1404	GAGGCAGGG	2436	RSDHLSR	2936	QSGSLTR	3436	RSDNLAR	3936	0.022

1405	GAGGCAGGG	2437	RSDHLSR	2937	QSGDLTR	3437	RSDNLAR	3937	0.045

1406	GAAGCGGAG	2438	RSDNLAR	2938	RSDELTR	3438	QSGNLAR	3938	0.025

1407	GCGGGCGCA	2439	QSGSLTR	2939	DRSHLAR	3439	RSDERKR	3939	0.585

1408	CCGGCAGGG	2440	RSDHLSR	2940	QSGSLTR	3440	RSDELRE	3940	0.305

1409	CCGGCAGGG	2441	RSDHLSR	2941	QSGSLTR	3441	RSDDLRE	3941	0.153

1410	CCGGCGGCG	2442	RSDELTR	2942	RSDELQR	3442	RSDELRE	3942	0.814

1411	TGAGGCGAG	2443	RSDNLAR	2943	DRSHLAR	3443	QSGHLTK	3943	0.282

1412	CTGGCCGTG	2444	RSDSLLR	2944	ERGTLAR	3444	RSDALRE	3944	0.172

1413	CTGGCCGCG	2445	RSDELTR	2945	DRSDLTR	3445	RSDALRE	3945	0.152

1414	CTGGCCGCG	2446	RSDELTR	2946	ERGTLAR	3446	RSDALRE	3946	0.914

1415	GCGGCCGAG	2447	RSDNLAR	2947	DRSDLTR	3447	RSDELQR	3947	0.102

1416	GCGGCCGAG	2448	RSDNLAR	2948	ERGTLAR	3448	RSDELQR	3948	0.153

1417	GAGTTGGCC	2449	ERGTLAR	2949	RGDALTS	3449	RSDNLAR	3949	1.397

1418	CTGGAGTTG	2450	RADALMV	2950	RSDNLAR	3450	RSDALRE	3950	0.241

1422	GGGTCGGCG	2451	RSDELTR	2951	RSDDLTT	3451	RSDHLSR	3951	0.064

1423	GGGTCGGCG	2452	RSDELTR	2952	RSDDLTK	3452	RSDHLSR	3952	0.034

1424	CAGGGCCCG	2453	RSDELRE	2953	DRSHLAR	3453	RSDNLRE	3953	1.37

1427	CAGGGCCCG	2454	RSDDLRE	2954	DRSHLAR	3454	RSDNLTE	3954	0.271

1428	TGAGGCGAG	2455	RSDNLAR	2955	DRSHLAR	3455	QSVHLQS	3955	0.102

1429	TGAGGCGAG	2456	RSDNLAR	2956	DRSHLAR	3456	QSGHLTT	3956	0.074

1430	TCGGCCGCC	2457	ERGTLAR	2957	DRSDLTR	3457	RSDDLTK	3957	0.352

1431	TCGGCCGCC	2458	ERGTLAR	2958	DRSDLTR	3458	RSDDLAS	3958	6.17

1432	TCGGCCGCC	2459	ERGTLAR	2959	ERGTLAR	3459	RSDDLTK	3959	1.778

1434	CTGGCCGTG	2460	RSDSLLR	2960	DRSDLTR	3460	RSDALRE	3960	0.051

1435	TAATGGGGG	2461	RSDHLSR	2961	RSDHLTT	3461	QSGNLTK	3961	0.057

1436	TGGGAGTGT	2462	TSDHLAS	2962	RSDNLAR	3462	RSDHLTT	3962	0.026

1439	GGAGTGTTA	2463	QRSALAS	2963	RSDALAR	3463	QSGHLQR	3963	0.075

1440	GGAGTGTTA	2464	QSGALTK	2964	RSDALAR	3464	QSGHLQR	3964	0.035

1441	ATAGCTGGG	2465	RSDHLSR	2965	QSSDLTR	3465	QSGALTQ	3965	0.262

1442	TGCTGGGCC	2466	ERGTLAR	2966	RSDHLTT	3466	DRSHLTK	3966	0.36

1443	TGGAAGGAA	2467	QSGNLAR	2967	RSDNLTQ	3467	RSHHLTT	3967	0.22

1444	TGGAAGGAA	2468	QSGNLAR	2968	RSDNLTQ	3468	RSSHLTT	3968	0.09

1445	TGGAAGGAA	2469	QSGNLAR	2969	RLDNLTA	3469	RSHHLTT	3969	0.182

1446	TGGAAGGAA	2470	QSGNLAR	2970	RLDNLTA	3470	RSSHLTT	3970	0.42

1454	GGAGAGGCT	2471	QSSDLRR	2971	RSDNLAR	3471	QSGHLQR	3971	0.01

1455	CGGGATGAA	2472	QSANLSR	2972	TSGNLVR	3472	RSDHLRE	3972	0.043

1456	GGAGAGGCT	2473	QSSDLRR	2973	RSDNLAR	3473	QRAHLAR	3973	0.016

1457	GCAGAGGAA	2474	QSANLSR	2974	RSDNTAR	3474	QSGSLTR	3974	0.014

1460	TTGGGGGAG	2475	RSDNLAR	2975	RSDHLTR	3475	RADALMV	3975	0.007

1461	GACGAGGAG	2476	RSANLAR	2976	RSDNLAR	3476	DRSNLTR	3976	0.014

1462	CGGGATGAA	2477	QSGNLAR	2977	TSGNLVR	3477	RSDHLRE	3977	0.05

1463	GAGGCTGTT	2478	TTSALTR	2978	QSSDLTR	3478	RSDNLAR	3978	0.003

1464	GACGAGGAG	2479	RSDNLAR	2979	RSDNLTR	3479	DRSNLTR	3979	0.002

1465	CTGGGAGTT	2480	TTSALTR	2980	QSGHLQR	3480	RSDALRE	3980	0.018

1466	CTGGGAGTT	2481	NRATLAR	2981	QSGHLQR	3481	RSDALRE	3981	0.017

1468	GGTGATGTC	2482	DRSALTR	2982	TSGNLVR	3482	MSHHLSR	3982	0.08

1469	GGTGATGTC	2483	DRSALTR	2983	TSGNLVR	3483	TSGHLVR	3983	0.28

1470	GGTGATGTC	2484	DRSALTR	2984	TSGNLVR	3484	QRAHLER	3984	0.156

1471	CTGGTTGGG	2485	RSDHLSR	2985	QSSALTR	3485	RSDALRE	3985	0.09

1472	TTGAAGGTT	2486	TTSALTR	2986	RSDNLTQ	3486	RADALMV	3986	3.22

1473	TTGAAGGTT	2487	TTSALTR	2987	RSDNLTQ	3487	RSDSLTT	3987	0.47

1474	TTGAAGGTT	2488	QSSALAR	2988	RSDNLTQ	3488	RADALMV	3988	1.39

1475	TTGAAGGTT	2489	QSSALAR	2989	RSDNLTQ	3489	RLHSLTT	3989	0.39

1476	TTGAAGGTT	2490	QSSALAR	2990	RSDNLTQ	3490	RSDSLTT	3990	0.305

1477	GCAGCCCGG	2491	RSDHLRE	2991	DRSDLTR	3491	QSGSLTR	3991	2.31

1479	GAAAGTTCA	2492	QSHDLTK	2992	MSHHLTQ	3492	QSGNLAR	3992	37.04

1480	GAAAGTTCA	2493	NKTDLGK	2993	TSGHLVQ	3493	QSGNLAR	3993	62.5

1481	GAAAGTTCA	2494	NKTDLGK	2994	TSDHLAS	3494	RSDELRE	3994	37.04

1482	CCGTGTGAC	2495	DRSNLTR	2995	TSDHLAS	3495	RSDELRE	3995	111.1

1483	CCGTGTGAC	2496	DRSNLTR	2996	MSHHLTT	3496	RSDELRE	3996	20.8

1484	GAAGTGGTA	2497	QSSSLVR	2997	RSDALSR	3497	QSGNLAR	3997	0.01

1485	AAGTGAGCT	2498	QSSDLRR	2998	QSGHLTT	3498	RSDNLTQ	3998	1.537

1486	GGGTTTGAC	2499	DRSNLTR	2999	TTSALAS	3499	RSDHLSR	3999	0.085

1487	TTGAAGGTT	2500	TTSALTR	3000	RSDNLTQ	3500	RLHSLTT	4000	0.188

1488	AAGTGGTAG	2501	QSSDLRR	3001	QSGHLTT	3501	RLDNRTQ	4001	5.64

1490	CTGGTTGGG	2502	RSDHLSR	3002	TSGSLTR	3502	RSDALRE	4002	0.04

1491	AAGGGTTCA	2503	NKTDLGK	3003	DSSKLSR	3503	RLDNRTA	4003	4.12

1492	AAGTGGTAG	2504	RSDNLTT	3004	RSDHLTT	3504	RSDNLTQ	4004	1.37

1493	AAGTGGTAG	2505	RSDNLTT	3005	RSDHLTT	3505	RLDNRTQ	4005	15.09

1494	GGGTTTGAC	2506	DRSNLTR	3006	QRSALAS	3506	RSDHLSR	4006	0.255

1496	TTGGGGGAG	2507	RSDNLAR	3007	RSDHLTR	3507	RSDALTT	4007	0.065

1497	GAGGCTCTT	2508	QSSALAR	3008	QSSDLTR	3508	RSDNLAR	4008	0.007

1498	GAGGTTGAT	2509	QSSNLAR	3009	QSSALTR	3509	RSDNLAR	4009	0.101

1499	GAGGTTGAT	2510	QSSNLAR	3010	TSGALTR	3510	RSDNLAR	4010	0.02

1500	GCAGAGGAA	2511	QSGNLAR	3011	RSDNLAR	3511	QSGSLTR	4011	0.003

1522	GCAATGGGT	2512	TSGHLVR	3012	RSDALTQ	3512	QSGDLTR	4012	0.08

[0120]

	TABLE 6


	FINGER (N→C)

TRIPLET (5′→3′)	F1	F2	F3

AGG			RXDHXXQ
ATG			RXDAXXQ
CGG			RXDHXXE
GAA		QXGNXXR
GAC	DXSNXXR		DXSNXXR
GAG	RXDNXXR	RXSNXXR	RXDNXXR
		RXDNXXR
GAT	QXSNXXR	TXGNXXR
	TXSNXXR
	TXGNXXR
GCA	QXGSXXR	QXGDXXR
GCC	EXGTXXR
GCG	RXDEXXR	RXDEXXR	RXDEXXR
			RXDTXXK
GCT	QXSDXXR	TXGEXXR
		QXSDXXR
GGA		QXGHXXR	QXAHXXR
GGC	DXSHXXR	DXSHXXR
GGG	RXDHXXR	RXDHXXR	RXDHXXR
			RXDHXXK
GGT			TXGHXXR
GTA		QXGSXXR
		QXATXXR
GTG	RXDAXXR	RXDAXXR	RXDAXXR
	RXDSXXR
TAG		RXDNXXT
TCG	RXDDXXK
TGT		TXDHXXS