Reaction participants Show >> << Hide
- Name help_outline (2S,3S)-hydroxyarginine Identifier CHEBI:73938 Charge 1 Formula C6H15N4O3 InChIKeyhelp_outline VIDUVSPOWYVZIC-IMJSIDKUSA-O SMILEShelp_outline NC(=[NH2+])NCC[C@H](O)[C@H]([NH3+])C([O-])=O 2D coordinates Mol file for the small molecule Search links Involved in 2 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline (2S,3R)-capreomycidine Identifier CHEBI:75665 Charge 1 Formula C6H13N4O2 InChIKeyhelp_outline XHNWDEHKMJLKGG-DMTCNVIQSA-O SMILEShelp_outline [NH3+][C@@H]([C@H]1CCNC(=[NH2+])N1)C([O-])=O 2D coordinates Mol file for the small molecule Search links Involved in 1 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline H2O Identifier CHEBI:15377 (Beilstein: 3587155; CAS: 7732-18-5) help_outline Charge 0 Formula H2O InChIKeyhelp_outline XLYOFNOQVPJJNP-UHFFFAOYSA-N SMILEShelp_outline [H]O[H] 2D coordinates Mol file for the small molecule Search links Involved in 6,204 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
Cross-references
| RHEA:38159 | RHEA:38160 | RHEA:38161 | RHEA:38162 | |
|---|---|---|---|---|
| Reaction direction help_outline | undefined | left-to-right | right-to-left | bidirectional |
| UniProtKB help_outline |
|
|||
| EC numbers help_outline | ||||
| KEGG help_outline | ||||
| MetaCyc help_outline |
Publications
-
Conversion of (2S)-arginine to (2S,3R)-capreomycidine by VioC and VioD from the viomycin biosynthetic pathway of Streptomyces sp. strain ATCC 11861.
Ju J., Ozanick S.G., Shen B., Thomas M.G.
ChemBioChem 5:1281-1285(2004) [PubMed] [EuropePMC]
This publication is cited by 1 other entry.
-
Formation of the nonproteinogenic amino acid 2S,3R-capreomycidine by VioD from the viomycin biosynthesis pathway.
Yin X., McPhail K.L., Kim K.J., Zabriskie T.M.