Protein Variants | Comment | Organism |
---|---|---|
D13A | significant decrease in the free energy of binding for the DehL-L-2-chloropropionic acid model complex, indicating the involvement of the residue in catalysis and/or structural integrity of the active site | Rhizobium sp. RC1 |
H184A | significant decrease in the free energy of binding for the DehL-L-2-chloropropionic acid model complex, indicating the involvement of the residue in catalysis and/or structural integrity of the active site | Rhizobium sp. RC1 |
M48A | significant decrease in the free energy of binding for the DehL-L-2-chloropropionic acid model complex, indicating the involvement of the residue in catalysis and/or structural integrity of the active site | Rhizobium sp. RC1 |
R51A | significant decrease in the free energy of binding for the DehL-L-2-chloropropionic acid model complex, indicating the involvement of the residue in catalysis and/or structural integrity of the active site | Rhizobium sp. RC1 |
T17A | significant decrease in the free energy of binding for the DehL-L-2-chloropropionic acid model complex, indicating the involvement of the residue in catalysis and/or structural integrity of the active site | Rhizobium sp. RC1 |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Rhizobium sp. RC1 | Q53187 | - |
- |
Reaction | Comment | Organism | Reaction ID |
---|---|---|---|
(S)-2-haloacid + H2O = (R)-2-hydroxyacid + halide | it is hypothesized that, in DehL, catalysis is initiated by a nucleophilic attack launched by the side-chain carboxyl of Asp13 on the C2 of L-2CP to form an ester intermediate, which is subsequently hydrolyzed by a water molecule activated by His184 followed by product release | Rhizobium sp. RC1 |
Synonyms | Comment | Organism |
---|---|---|
DehL | - |
Rhizobium sp. RC1 |
L-2-haloacid dehalogenase | - |
Rhizobium sp. RC1 |