| EC Tree |
| 2. Transferases |
| 2.6 Transferring nitrogenous groups |
| 2.6.99 Transferring other nitrogenous groups |
| ID: | 2.6.99.3 |
|---|---|
| Description: | O-ureido-L-serine synthase. |
| Cath: | 3.40.50.1100; |
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 2.6.99.3 |
| BRENDA Enzyme Link: | BRENDA 2.6.99.3 |
| KEGG Enzyme Link: | KEGG2.6.99.3 |
| BioCyc Enzyme Link: | BioCyc 2.6.99.3 |
| ExPASy Enzyme Link: | ExPASy2.6.99.3 |
| EC2PDB Enzyme Link: | EC2PDB 2.6.99.3 |
| ExplorEnz Enzyme Link: | ExplorEnz 2.6.99.3 |
| PRIAM enzyme-specific profiles Link: | PRIAM 2.6.99.3 |
| IntEnz Enzyme Link: | IntEnz 2.6.99.3 |
| MEDLINE Enzyme Link: | MEDLINE 2.6.99.3 |
| RHEA:36263 | hydroxyurea + O-acetyl-L-serine = acetate + H(+) + O-ureido-L-serine |
| RULE(radius=1) | [*:1]-[CH2;+0:2]-[O;H0;+0:3]-[*:4].[*:5]-[OH;+0:6]>>[*:5]-[O;H0;+0:6]-[CH2;+0:2]-[*:1].[*:4]-[OH;+0:3] |
| Reaction | ![]() |
| Core-to-Core | No scaffolds atoms were exchanged as a result of the reaction |
| Title | Authors | Date | PubMed ID |
|---|---|---|---|
| Establishment of an in vitro D-cycloserine-synthesizing system by using O-ureido-L-serine synthase and D-cycloserine synthetase found in the biosynthetic pathway. | Uda N, Matoba Y, Kumagai T, Oda K, Noda M, Sugiyama M | 2013 Jun | 23529730 |
| Molecular cloning and heterologous expression of a biosynthetic gene cluster for the antitubercular agent D-cycloserine produced by Streptomyces lavendulae. | Kumagai T, Koyama Y, Oda K, Noda M, Matoba Y, Sugiyama M | 2010 Mar | 20086163 |