Enzyme

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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
Description:Carboxymethylhydantoinase.

3D structure

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References

External Links

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
MSA:

3.5.2.4;

Phylogenetic Tree:

3.5.2.4;

Uniprot:
M-CSA:
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

References

TitleAuthorsDatePubMed ID
Enzymatic synthesis and breakdown of a pyrimidine, orotic acid. I. Dihydroortic acid, ureidosuccinic acid, and 5-carboxymethylhydantoin.LIEBERMAN I, KORNBERG A1954 Apr13163076