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Literature summary for 4.2.3.120 extracted from
- Stereochemistry of the proton elimination in the formation of (+)- and (-)-alpha-pinene by monoterpene cyclases from sage (Salvia officinalis) (1994), Arch. Biochem. Biophys., 308, 488-496.
Organism
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Salvia officinalis | - |
- |
- |
Substrates and Products (Substrate)
| Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| geranyl diphosphate | - |
Salvia officinalis | (-)-beta-pinene + diphosphate | products are (-)-alpha-pinene, (-)-beta-pinene, and (-)-camphene | ? |  |
| additional information | enzymes removes the C4-proS-hydrogen of the substrate, the C3 proton of the corresponding pinyl cation, with a stereoselectivity exceeding 78% in the formation of (-)-alpha-pinene | Salvia officinalis | ? | - |
? | |
Synonyms
| Synonyms | Comment | Organism |
|---|---|---|
| cyclase II | - |
Salvia officinalis |
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