ID: | 3.7.1.12 |
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Description: | Cobalt-precorrin 5A hydrolase. |
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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 3.7.1.12 |
BRENDA Enzyme Link: | BRENDA 3.7.1.12 |
KEGG Enzyme Link: | KEGG3.7.1.12 |
BioCyc Enzyme Link: | BioCyc 3.7.1.12 |
ExPASy Enzyme Link: | ExPASy3.7.1.12 |
EC2PDB Enzyme Link: | EC2PDB 3.7.1.12 |
ExplorEnz Enzyme Link: | ExplorEnz 3.7.1.12 |
PRIAM enzyme-specific profiles Link: | PRIAM 3.7.1.12 |
IntEnz Enzyme Link: | IntEnz 3.7.1.12 |
MEDLINE Enzyme Link: | MEDLINE 3.7.1.12 |
RHEA:26281 | Co-precorrin-5A + H2O = acetaldehyde + Co-precorrin-5B + H(+) |
RULE(radius=1) | [*:1]-[C;H0;+0:2](=[C;H0;+0:3](-[*:4])-[*:5])-[C;H0;+0:6](-[*:7])(-[*:8])-[CH;+0:9](-[*:10])-[O;H0;+0:11]-[*:12].[OH2;+0:13]>>([*:1]-[C;H0;+0:2](=[C;H0;+0:6](-[*:7])-[*:8])-[CH;+0:3](-[*:4])-[*:5].[*:12]-[OH;+0:11]).[*:10]-[CH;+0:9]=[O;H0;+0:13] |
Reaction | ![]() |
Core-to-Core |
Title | Authors | Date | PubMed ID |
---|---|---|---|
Genetically engineered synthesis and structural characterization of cobalt-precorrin 5A and -5B, two new intermediates on the anaerobic pathway to vitamin B12: definition of the roles of the CbiF and CbiG enzymes. | Kajiwara Y, Santander PJ, Roessner CA, Pérez LM, Scott AI | 2006 Aug 2 | 16866557 |