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Literature summary for 4.2.3.7 extracted from
- Theoretical studies on farnesyl cation cyclization: pathways to pentalenene (2006), J. Am. Chem. Soc., 128, 6172-6179.
Natural Substrates/ Products (Substrates)
| Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| 2-trans,6-trans-farnesyl diphosphate | Streptomyces exfoliatus | the study describes theoretical studies on the cyclization reaction | pentalenene + diphosphate | - |
? |  |
Organism
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Streptomyces exfoliatus | Q55012 | in this theoretical study Streptomyces is given as an example for a pentalenene synthesizing organism | - |
Substrates and Products (Substrate)
| Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| 2-trans,6-trans-farnesyl diphosphate | the study describes theoretical studies on the cyclization reaction | Streptomyces exfoliatus | pentalenene + diphosphate | - |
? | |
Synonyms
| Synonyms | Comment | Organism |
|---|---|---|
| pentalenene synthase | - |
Streptomyces exfoliatus |
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