10-Formyltetrahydrofolate (10-CHO-THF) is a form oftetrahydrofolate that acts as a donor offormyl groups inanabolism. In these reactions 10-CHO-THF is used as asubstrate in formyltransferase reactions.
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Names | |
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Preferred IUPAC name (2S)-2-[4-(N-{[(6Ξ)-2-Amino-4-oxo-1,4,5,6,7,8-hexahydropteridin-6-yl]methyl}formamido)benzamido]pentanedioic acid | |
Other names
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MeSH | 10-formyl-tetrahydrofolate |
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Properties | |
C20H23N7O7 | |
Molar mass | 473.44 g/mol |
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). |
Functions
editTwo equivalents of 10-CHO-THF are required inpurine biosynthesis through thepentose phosphate pathway, where 10-CHO-THF is a substrate forphosphoribosylaminoimidazolecarboxamide formyltransferase.
10-CHO-THF is required for the formylation ofmethionyl-tRNA formyltransferase to givefMet-tRNA.[1]
Formation from methenyltetrahydrofolate
edit10-CHO-THF is produced frommethylenetetrahydrofolate (CH2H4F) via a two step process. The first step generates5,10-methenyltetrahydrofolate:[2]
- CH2H4F + NAD+ CH2H2F + NADH + H+
In the second step 5,10-methenyltetrahydrofolate undergoes hydrolysis:
- CH2H2F + H2O CHO-H4F +
The latter is equivalently written:
- 5,10-methenyltetrahydrofolate + H2O 10-formyltetrahydrofolate
10-CHO-THF is also produced by the reaction
- ATP +formate + tetrahydrofolate ADP + phosphate + 10-formyltetrahydrofolate
This reaction is catalyzed byformate-tetrahydrofolate ligase.
It can be converted back intotetrahydrofolate (THF) byformyltetrahydrofolate dehydrogenase or THF and formate byformyltetrahydrofolate deformylase.
References
edit- ^Voet, Donald (2016).Fundamentals of Biochemistry: Life at the Molecular Level (5th ed.). Wiley. pp. 1006–1007.ISBN 978-1-118-91840-1.
- ^Peter D. Pawelek; Robert E. MacKenzie (1998). "Methenyltetrahydrofolate Cyclohydrolase Is Rate Limiting for the Enzymatic Conversion of 10-Formyltetrahydrofolate to 5,10-Methylenetetrahydrofolate in Bifunctional Dehydrogenase-Cyclohydrolase Enzymes".Biochemistry.37 (4):1109–1115.doi:10.1021/bi971906t.PMID 9454603.