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2.1.2.8: deoxycytidylate 5-hydroxymethyltransferase

This is an abbreviated version!
For detailed information about deoxycytidylate 5-hydroxymethyltransferase, go to the full flat file.

Word Map on EC 2.1.2.8

Reaction

5,10-methylenetetrahydrofolate
+
H2O
+
deoxycytidylate
=
tetrahydrofolate
+
5-hydroxymethyldeoxycytidylate

Synonyms

d-cytidine 5'-monophosphate hydroxymethylase, DCH, dCMP Hmase, dCMP hydroxymethylase, deoxyCMP hydroxymethylase, deoxycytidylate hydroxymethylase, deoxycytidylate hydroxymethyltransferase, deoxycytidylic hydroxymethylase, hydroxymethyltransferase, deoxycytidylate

ECTree

     2 Transferases
         2.1 Transferring one-carbon groups
             2.1.2 Hydroxymethyl-, formyl- and related transferases
                2.1.2.8 deoxycytidylate 5-hydroxymethyltransferase

Inhibitors

Inhibitors on EC 2.1.2.8 - deoxycytidylate 5-hydroxymethyltransferase

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INHIBITOR
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
10-methyl-5,8-dideazatetrahydrofolate
Tequatrovirus T4
-
competitive inhibitor with respect to tetrahydrofolate
5,5'-dithiobis(2-nitrobenzoic acid)
Tequatrovirus T4
-
complete loss of activity, second-order kinetics, inactivation is reversed by dithiothreitol, inactivation involves the modification of one thiol group per mol of dimeric enzyme
5-deazatetrahydrofolate
5-Fluoro-2'-deoxycytidine 5'-monophosphate
Tequatrovirus T4
-
competitive inhibitor with respect to dCMP, not mechanism-based inhibitor
5-fluorodeoxyuridylate
5-hydroxymethyl-dCMP
Tequatrovirus T4
-
competitor of dCMP, inhibits formation of 5-hydroxymethyl-dCMP
aminopterin
Tequatrovirus T4
-
competitive inhibitor with respect to tetrahydrofolate
dihydrofolate
Tequatrovirus T4
-
competitive inhibitor with respect to tetrahydrofolate
methotrexate
Tequatrovirus T4
-
competitive inhibitor with respect to tetrahydrofolate
N-ethylmaleimide
Tequatrovirus T4
-
complete loss of activity, second-order kinetics, pH-dependent inactivation, dCMP protects against inactivation, dCMP plus either methotrexate or aminopterin greatly enhances protection, inactivation involves the modification of one thiol group per mol of dimeric enzyme