ID: | 4.2.1.145 |
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Description: | Capreomycidine synthase. |
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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 4.2.1.145 |
BRENDA Enzyme Link: | BRENDA 4.2.1.145 |
KEGG Enzyme Link: | KEGG4.2.1.145 |
BioCyc Enzyme Link: | BioCyc 4.2.1.145 |
ExPASy Enzyme Link: | ExPASy4.2.1.145 |
EC2PDB Enzyme Link: | EC2PDB 4.2.1.145 |
ExplorEnz Enzyme Link: | ExplorEnz 4.2.1.145 |
PRIAM enzyme-specific profiles Link: | PRIAM 4.2.1.145 |
IntEnz Enzyme Link: | IntEnz 4.2.1.145 |
MEDLINE Enzyme Link: | MEDLINE 4.2.1.145 |
MSA: | |
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Phylogenetic Tree: | |
Uniprot: | |
M-CSA: |
RHEA:38159 | (2S,3S)-hydroxyarginine = (2S,3R)-capreomycidine + H2O |
RULE(radius=1) | ([*:1]-[CH;+0:2](-[*:3])-[OH;+0:4].[*:5]-[NH2;+0:6])>>[*:5]-[NH;+0:6]-[CH;+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 |
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Conversion of (2S)-arginine to (2S,3R)-capreomycidine by VioC and VioD from the viomycin biosynthetic pathway of Streptomyces sp. strain ATCC11861. | Ju J, Ozanick SG, Shen B, Thomas MG | 2004 Sep 6 | 15368582 |
Formation of the nonproteinogenic amino acid 2S,3R-capreomycidine by VioD from the viomycin biosynthesis pathway. | Yin X, McPhail KL, Kim KJ, Zabriskie TM | 2004 Sep 6 | 15368581 |