Any feedback?
Literature summary extracted from
- Structure and reactivity of the dammarenyl cation: configurational transmission in triterpene synthesis (2005), J. Org. Chem., 70, 5362-5375.
Organism
| EC Number | Organism | UniProt | Comment | Textmining |
|---|---|---|---|---|
| 5.4.99.41 | Arabidopsis thaliana | - |
- |
- |
Reaction
| EC Number | Reaction | Comment | Organism | Reaction ID |
|---|---|---|---|---|
| 5.4.99.41 | (3S)-2,3-epoxy-2,3-dihydrosqualene = lupeol | the C17 configuration of the tetracyclic intermediate dammarenyl cation can be deduced from the angular methyl configuration of the pentacyclic or 6-6-6-6 tetracyclic product | Arabidopsis thaliana |
Substrates and Products (Substrate)
| EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|---|
| 5.4.99.41 | (18E)-22,23-dihydro-20-oxa-oxidosqualene | the 20-oxa substitution has negligible effect on substrate binding and on the activation energies | Arabidopsis thaliana | 3beta-hydroxy-22,23,24,25,26,27-hexanor-17beta-dammaran-20-one + ? | sole product | ? |  |
| 5.4.99.41 | 2,3-oxidosqualene | - |
Arabidopsis thaliana | lupeol | - |
? | |
Use of this online version of BRENDA is free under the CC BY 4.0 license. See terms of use for full details.
Release 2023.1 (January 2023)
Legal
Curated at
Member of
