EC Tree |
3. Hydrolases |
3.5 Acting on carbon-nitrogen bonds, other than peptide bonds |
3.5.2 In cyclic amides |
ID: | 3.5.2.4 |
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Description: | Carboxymethylhydantoinase. |
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Note: Use your mouse to drag, rotate, and zoom in and out of the structure. Mouse-over to identify atoms and bonds. Mouse controls documentation.UniProtKB Enzyme Link: | UniProtKB 3.5.2.4 |
BRENDA Enzyme Link: | BRENDA 3.5.2.4 |
KEGG Enzyme Link: | KEGG3.5.2.4 |
BioCyc Enzyme Link: | BioCyc 3.5.2.4 |
ExPASy Enzyme Link: | ExPASy3.5.2.4 |
EC2PDB Enzyme Link: | EC2PDB 3.5.2.4 |
ExplorEnz Enzyme Link: | ExplorEnz 3.5.2.4 |
PRIAM enzyme-specific profiles Link: | PRIAM 3.5.2.4 |
IntEnz Enzyme Link: | IntEnz 3.5.2.4 |
MEDLINE Enzyme Link: | MEDLINE 3.5.2.4 |
RHEA:12028 | H2O + L-5-carboxymethylhydantoin = H(+) + N-carbamoyl-L-aspartate |
RULE(radius=1) | ([*:1]-[C;H0;+0:2](=[*:3])-[OH;+0:4].[*:5]-[NH2;+0:6]).[H+;H0:7]>>[*:5]-[NH;+0:6]-[C;H0;+0:2](-[*:1])=[*:3].[OH2;+0:4] |
Reaction | ![]() |
Core-to-Core | No scaffolds atoms were exchanged as a result of the reaction |
Title | Authors | Date | PubMed ID |
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Enzymatic synthesis and breakdown of a pyrimidine, orotic acid. I. Dihydroortic acid, ureidosuccinic acid, and 5-carboxymethylhydantoin. | LIEBERMAN I, KORNBERG A | 1954 Apr | 13163076 |