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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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Identifiers | |
3D model (JSmol) |
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ChemSpider | |
KEGG |
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MeSH | 10-formyl-tetrahydrofolate |
PubChem CID |
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CompTox Dashboard (EPA) |
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Properties | |
C20H23N7O7 | |
Molar mass | 473.44 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
10-Formyltetrahydrofolate (10-CHO-THF) is a form of tetrahydrofolate that acts as a donor of formyl groups in anabolism. In these reactions 10-CHO-THF is used as a substrate in formyltransferase reactions.
Two equivalents of 10-CHO-THF are required in purine biosynthesis through the pentose phosphate pathway, where 10-CHO-THF is a substrate for phosphoribosylaminoimidazolecarboxamide formyltransferase.
10-CHO-THF is required for the formylation of methionyl-tRNA formyltransferase to give fMet-tRNA.[1]
10-CHO-THF is produced from methylenetetrahydrofolate (CH2H4F) via a two step process. The first step generates 5,10-methenyltetrahydrofolate:[2]
In the second step 5,10-methenyltetrahydrofolate undergoes hydrolysis:
The latter is equivalently written:
10-CHO-THF is also produced by the reaction
This reaction is catalyzed by formate-tetrahydrofolate ligase.
It can be converted back into tetrahydrofolate (THF) by formyltetrahydrofolate dehydrogenase or THF and formate by formyltetrahydrofolate deformylase.