| 10-Formyltetrahydrofolate | |
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(2S)-2-{[4-[(2-amino-4-oxo-5,6,7,8-tetrahydro-1H-pteridin-6-yl)
methyl(formyl)amino]benzoyl]amino}pentanedioic acid |
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Other names
10-CHO-THF
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| Identifiers | |
| CAS number | 2800-34-2 |
| PubChem | 10 |
| ChemSpider | 9 |
| MeSH | 10-formyl-tetrahydrofolate |
| Jmol-3D images | Image 1 Image 2 |
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| Properties | |
| Molecular formula | C20H23N7O7 |
| Molar mass | 473.44 g/mol |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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| Infobox references | |
10-Formyltetrahydrofolate (10-CHO-THF) is 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. This is important in purine biosynthesis, where 10-CHO-THF is a substrate for phosphoribosylaminoimidazolecarboxamide formyltransferase, as well as in the formylation of the methionyl initiator tRNA (fMet-tRNA), when 10-CHO-THF is a substrate for methionyl-tRNA formyltransferase.
10-CHO-THF is produced either by the enzyme methenyltetrahydrofolate cyclohydrolase via the reaction
10-formyltetrahydrofolateand by the enzyme formate-tetrahydrofolate ligase via the reaction
ADP + phosphate + 10-formyltetrahydrofolateIt can be converted back into tetrahydrofolate (THF) by formyltetrahydrofolate dehydrogenase or THF and formate by formyltetrahydrofolate deformylase.
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