ID: | 4.1.2.11 |
---|---|
Description: | Hydroxymandelonitrile lyase. |
Alternative Name: |
Hydroxynitrile lyase. (S)-4-hydroxymandelonitrile hydroxybenzaldehyde-lyase. |
Cath: | 1.20.5.2390; 3.40.50.11320; 3.40.50.1820; |
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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 4.1.2.11 |
BRENDA Enzyme Link: | BRENDA 4.1.2.11 |
KEGG Enzyme Link: | KEGG4.1.2.11 |
BioCyc Enzyme Link: | BioCyc 4.1.2.11 |
ExPASy Enzyme Link: | ExPASy4.1.2.11 |
EC2PDB Enzyme Link: | EC2PDB 4.1.2.11 |
ExplorEnz Enzyme Link: | ExplorEnz 4.1.2.11 |
PRIAM enzyme-specific profiles Link: | PRIAM 4.1.2.11 |
IntEnz Enzyme Link: | IntEnz 4.1.2.11 |
MEDLINE Enzyme Link: | MEDLINE 4.1.2.11 |
RHEA:15977 | (S)-4-hydroxymandelonitrile = 4-hydroxybenzaldehyde + hydrogen cyanide |
RULE(radius=1) | [*:1]#[C;H0;+0:2]-[CH;+0:3](-[*:4])-[OH;+0:5]>>[*:1]#[CH;+0:2].[*:4]-[CH;+0:3]=[O;H0;+0:5] |
Reaction | ![]() |
Core-to-Core | No scaffolds atoms were exchanged as a result of the reaction |
Title | Authors | Date | PubMed ID |
---|---|---|---|
Crystal structure of hydroxynitrile lyase from Sorghum bicolor in complex with the inhibitor benzoic acid: a novel cyanogenic enzyme. | Lauble H, Miehlich B, Förster S, Wajant H, Effenberger F | 2002 Oct 8 | 12356304 |