P450 Protein:
| P450 Symbol | CYP72A61v2 |
| Protein Name | Cytochrome P450 monooxygenase |
| Uniprot ID | H1A985 |
| Species | Medicago truncatula (Barrel medic) (Medicago tribuloides) |
| Txid | 3880 |
| P450 Protein Structure |
Model Confidence (pLDDT)
Very high (>90)
High (90 > 70)
Low (70 > 50)
Very low (<50)
|
| Subcellular Location | / |
| Protein Sequence | GO |
Reaction Scheme:
| Chemical Conversion | C30H50O2 → C30H50O3 |
| Reaction Type | Oxidation |
| Chemical Bond | CH2 |
CYP72A61v2
Substrate Information:
| Substrate Name | 24-Hydroxy-Beta-Amyrin |
| Substrate Chemical Formula | C30H50O2 |
| Substrate PubChem CID | 14167253 |
| Substrate Smiles | C[C@@]12CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H]([C@]5(C)CO)O)C)C)[C@@H]1CC(CC2)(C)C)C |
| Substrate Structure |
Product Information:
| Product Name | Soyasapogenol B |
| Product Chemical Formula | C30H50O3 |
| Product PubChem CID | 115012 |
| Product Smiles | C[C@]12CC[C@@H]([C@]([C@@H]1CC[C@@]3([C@@H]2CC=C4[C@]3(CC[C@@]5([C@H]4CC(C[C@H]5O)(C)C)C)C)C)(C)CO)O |
| Product Structure |
References:
| Title: | Combinatorial biosynthesis of legume natural and rare triterpenoids in engineered yeast. |
| PMID: | 23378447 |
| Journal: | Plant & cell physiology |
| Year: | 2013/5/1 |