10-Formyltetrahydrofolate

10-Formyltetrahydrofolate
Names
	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 10-CHO-THF; 10-FormylH4folate; N10-Formyltetrahydrofolate;
Identifiers
CAS Number	2800-34-2 ;
3D model (JSmol)	Interactive image;
ChemSpider	109092 ;
KEGG	C00234;
MeSH	10-formyl-tetrahydrofolate
PubChem CID	135450591;
CompTox Dashboard (EPA)	DTXSID60903987 ;
	InChI InChI=1S/C20H23N7O7/c21-20-25-16-15(18(32)26-20)23-11(7-22-16)8-27(9-28)12-3-1-10(2-4-12)17(31)24-13(19(33)34)5-6-14(29)30/h1-4,9,11,13,23H,5-8H2,(H,24,31)(H,29,30)(H,33,34)(H4,21,22,25,26,32)/t11?,13-/m0/s1 Key: AUFGTPPARQZWDO-YUZLPWPTSA-N ;
	SMILES c1cc(ccc1C(=O)N[C@@H](CCC(=O)O)C(=O)O)N(CC2CNc3c(c(=O)nc([nH]3)N)N2)C=O;
Properties
Chemical formula	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). verify (what is ?) Infobox references

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.

Functions

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]

Formation from methenyltetrahydrofolate

10-CHO-THF is produced from methylenetetrahydrofolate (CH₂H₄F) via a two step process. The first step generates 5,10-methenyltetrahydrofolate:^[2]

CH₂H₄F + NAD⁺

\rightleftharpoons

CH₂H₂F + NADH + H⁺

In the second step 5,10-methenyltetrahydrofolate undergoes hydrolysis:

CH₂H₂F + H₂O

\rightleftharpoons

CHO-H₄F +

The latter is equivalently written:

5,10-methenyltetrahydrofolate + H₂O

\rightleftharpoons

10-formyltetrahydrofolate

10-CHO-THF is also produced by the reaction

ATP + formate + tetrahydrofolate

\rightleftharpoons

ADP + phosphate + 10-formyltetrahydrofolate

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.

References

^ 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.

[1] Voet, Donald (2016). Fundamentals of Biochemistry: Life at the Molecular Level (5th ed.). Wiley. pp. 1006–1007. ISBN 978-1-118-91840-1.

[2] 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.

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