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Literature summary for 4.1.2.47 extracted from
- Electrospray ionization mass spectrometry, circular dichroism and SAXS studies of the (S)-hydroxynitrile lyase from Hevea brasiliensis (2001), Biochim. Biophys. Acta, 1544, 133-142.
Crystallization (Commentary)
| Crystallization (Comment) | Organism |
|---|---|
- |
Hevea brasiliensis |
Molecular Weight [Da]
| Molecular Weight [Da] | Molecular Weight Maximum [Da] | Comment | Organism |
|---|---|---|---|
| 29210 | - |
electrospray mass spectrometry | Hevea brasiliensis |
Natural Substrates/ Products (Substrates)
| Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| 2-hydroxy-2-methylpropanenitrile | Hevea brasiliensis | - |
HCN + acetone | - |
? |  |
Organism
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Hevea brasiliensis | - |
rubber tree | - |
Substrates and Products (Substrate)
| Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| (S)-mandelonitrile | highly (S)-selective | Hevea brasiliensis | HCN + benzaldehyde | - |
? | |
| 2-hydroxy-2-methylpropanenitrile | - |
Hevea brasiliensis | HCN + acetone | - |
? | |
| 2-hydroxy-2-methylpropanenitrile | liberation of HCN by degradation of acetone cyanohydrin is considerably faster than the consumption of HCN by the formation of (S)-mandelonitrile | Hevea brasiliensis | HCN + acetone | - |
? | |
Synonyms
| Synonyms | Comment | Organism |
|---|---|---|
| (S)-Hydroxynitrile lyase | - |
Hevea brasiliensis |
| (S)-selective hydroxynitrile lyase | - |
Hevea brasiliensis |
pH Stability
| pH Stability | pH Stability Maximum | Comment | Organism |
|---|---|---|---|
| 6 | - |
very stable above pH 6.0 | Hevea brasiliensis |
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