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Literature summary extracted from
- A new approach for the investigation of isoprenoid biosynthesis featuring pathway switching, deuterium hyperlabeling, and 1H NMR spectroscopy. The reaction mechanism of a novel streptomyces diterpene cyclase (2003), J. Org. Chem., 68, 5433-5438.
Organism
| EC Number | Organism | UniProt | Comment | Textmining |
|---|---|---|---|---|
| 4.2.3.36 | Kitasatospora griseola | - |
- |
- |
| 5.5.1.15 | Streptomyces lividans | - |
- |
- |
Substrates and Products (Substrate)
| EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|---|
| 4.2.3.36 | terpentedienyl diphosphate | - |
Kitasatospora griseola | terpentetriene + diphosphate | - |
? |  |
| 5.5.1.15 | geranylgeranyl diphosphate | the triggering proton is lost at the end of the cyclization reaction | Streptomyces lividans | terpentedienyl diphosphate | - |
? | |
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Release 2023.1 (January 2023)
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