EC Number | Application | Comment | Organism |
---|---|---|---|
4.1.2.47 | synthesis | production of chiral ferrocene derivatives as ligands in asymmetric catalysis, to bioelectrochemistry and development of new pharmaceuticals against malaria | Hevea brasiliensis |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
4.1.2.47 | Hevea brasiliensis | - |
- |
- |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
4.1.2.47 | acetone cyanhydrin | - |
Hevea brasiliensis | HCN + acetone | - |
? | |
4.1.2.47 | HCN + 1,1'-diformylferrocene | - |
Hevea brasiliensis | (R,R)-1,1-bis(cyanohydroxymethyl)ferrocene | - |
? | |
4.1.2.47 | HCN + ferrocene aldehyde | - |
Hevea brasiliensis | ? | - |
? | |
4.1.2.47 | HCN + formylferrocene | - |
Hevea brasiliensis | (R)-(cyanohydroxymethyl)ferrocene | - |
? | |
4.1.2.47 | additional information | acetylferrocene and 1,1'-diacetylferrocene are not transformed with this enzyme | Hevea brasiliensis | ? | - |
? |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
4.1.2.47 | (S)-HbHNL | - |
Hevea brasiliensis |
4.1.2.47 | Hydroxynitrile lyase | - |
Hevea brasiliensis |
EC Number | pH Optimum Minimum | pH Optimum Maximum | Comment | Organism |
---|---|---|---|---|
4.1.2.47 | 4.8 | - |
conversion of formylferrocene | Hevea brasiliensis |
EC Number | pH Stability | pH Stability Maximum | Comment | Organism |
---|---|---|---|---|
4.1.2.47 | 4.8 | - |
still stable at this value | Hevea brasiliensis |