EC number:3.5.1.110
Enzyme
Download| EC Tree |
| 3. Hydrolases |
| 3.5 Acting on carbon-nitrogen bonds, other than peptide bonds |
| 3.5.1 In linear amides |
| ID: | 3.5.1.110 |
|---|---|
| Description: | Peroxyureidoacrylate/ureidoacrylate amidohydrolase. |
3D structure
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External Links
| UniProtKB Enzyme Link: | UniProtKB 3.5.1.110 |
| BRENDA Enzyme Link: | BRENDA 3.5.1.110 |
| KEGG Enzyme Link: | KEGG3.5.1.110 |
| BioCyc Enzyme Link: | BioCyc 3.5.1.110 |
| ExPASy Enzyme Link: | ExPASy3.5.1.110 |
| EC2PDB Enzyme Link: | EC2PDB 3.5.1.110 |
| ExplorEnz Enzyme Link: | ExplorEnz 3.5.1.110 |
| PRIAM enzyme-specific profiles Link: | PRIAM 3.5.1.110 |
| IntEnz Enzyme Link: | IntEnz 3.5.1.110 |
| MEDLINE Enzyme Link: | MEDLINE 3.5.1.110 |
EC number:3.5.1.110
| MSA: | |
|---|---|
| Phylogenetic Tree: | |
| Uniprot: | |
| M-CSA: |
| RHEA:42624 | (Z)-3-ureidoacrylate + H(+) + H2O = (Z)-3-aminoacrylate + CO2 + NH4(+) |
| RULE(radius=1) | [*:1]-[NH;+0:2]-[C;H0;+0:3](=[*:4])-[NH2;+0:5].[H+;H0:6].[OH2;+0:7]>>[*:1]-[NH2;+0:2].[*:4]=[C;H0;+0:3]=[O;H0;+0:7].[NH3;+0:5] |
| Reaction |  |
| Core-to-Core | No scaffolds atoms were exchanged as a result of the reaction |
References
| Title | Authors | Date | PubMed ID |
|---|---|---|---|
| The Rut pathway for pyrimidine degradation: novel chemistry and toxicity problems. | Kim KS, Pelton JG, Inwood WB, Andersen U, Kustu S, Wemmer DE | 2010 Aug | 20400551 |
| RHEA:42620 | (Z)-2-methyl-ureidoacrylate peracid + H(+) + H2O = (Z)-2-hydroxy-3-aminoperacrylic acid + CO2 + NH4(+) |
| RULE(radius=1) | [*:1]=[C;H0;+0:2](-[NH2;+0:3])-[NH;+0:4]-[*:5].[H+;H0:6].[OH2;+0:7]>>[*:5]-[NH2;+0:4].[*:1]=[C;H0;+0:2]=[O;H0;+0:7].[NH3;+0:3] |
| Reaction |  |
| Core-to-Core | No scaffolds atoms were exchanged as a result of the reaction |
References
| Title | Authors | Date | PubMed ID |
|---|---|---|---|
| The Rut pathway for pyrimidine degradation: novel chemistry and toxicity problems. | Kim KS, Pelton JG, Inwood WB, Andersen U, Kustu S, Wemmer DE | 2010 Aug | 20400551 |
| RHEA:42616 | (Z)-3-ureidoacrylate peracid + H(+) + H2O = (Z)-3-aminoperacrylic acid + CO2 + NH4(+) |
| RULE(radius=1) | [*:1]-[NH;+0:2]-[C;H0;+0:3](=[*:4])-[NH2;+0:5].[OH2;+0:6]>>[*:1]-[NH2;+0:2].[*:4]=[C;H0;+0:3]=[O;H0;+0:6].[NH3;+0:5] |
| Reaction |  |
| Core-to-Core | No scaffolds atoms were exchanged as a result of the reaction |
References
| Title | Authors | Date | PubMed ID |
|---|---|---|---|
| The Rut pathway for pyrimidine degradation: novel chemistry and toxicity problems. | Kim KS, Pelton JG, Inwood WB, Andersen U, Kustu S, Wemmer DE | 2010 Aug | 20400551 |