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
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2.1.2.8
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bacteriophage
-
phage
-
thymidylate
-
amber
-
deoxyribonucleotide
-
triphosphate
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dtmp
-
dihydrofolate
-
phage-coded
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cytosine
-
ribonucleotide
-
fork
-
t4-infected
-
dctpase
- 2.1.2.8
- bacteriophage
- phage
- thymidylate
-
amber
- deoxyribonucleotide
- triphosphate
- dtmp
- dihydrofolate
-
phage-coded
- cytosine
- ribonucleotide
-
fork
-
t4-infected
- dctpase
Reaction
Synonyms
d-cytidine 5'-monophosphate hydroxymethylase, DCH, dCMP Hmase, dCMP hydroxymethylase, deoxyCMP hydroxymethylase, deoxycytidylate hydroxymethylase, deoxycytidylate hydroxymethyltransferase, deoxycytidylic hydroxymethylase, hydroxymethyltransferase, deoxycytidylate
ECTree
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Inhibitors
Inhibitors on EC 2.1.2.8 - deoxycytidylate 5-hydroxymethyltransferase
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10-methyl-5,8-dideazatetrahydrofolate
Tequatrovirus T4
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competitive inhibitor with respect to tetrahydrofolate
5,5'-dithiobis(2-nitrobenzoic acid)
Tequatrovirus T4
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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-Fluoro-2'-deoxycytidine 5'-monophosphate
Tequatrovirus T4
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competitive inhibitor with respect to dCMP, not mechanism-based inhibitor
5-hydroxymethyl-dCMP
Tequatrovirus T4
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competitor of dCMP, inhibits formation of 5-hydroxymethyl-dCMP
N-ethylmaleimide
Tequatrovirus T4
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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
Tequatrovirus T4
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competitive inhibitor with respect to tetrahydrofolate
Tequatrovirus T4
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inactivates by formation of a covalent complex containing enzyme, inhibitor and methylenetetrahydrofolate in a time-dependent manner, 1 mol 5-fluoro-dUMP per enzyme monomer, no substantial inhibition of wild-type enzyme in vivo, inhibition mechanism