| 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. |
Click one PDB to see exact 3D structure provided by NGL.
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 |
|---|---|---|---|
| Enzymatic synthesis and breakdown of a pyrimidine, orotic acid. I. Dihydroortic acid, ureidosuccinic acid, and 5-carboxymethylhydantoin. | LIEBERMAN I, KORNBERG A | 1954 Apr | 13163076 |