P450 Protein:
| P450 Symbol | |
| Protein Name | P450Um-1 |
| Uniprot ID | Q59HJ0 |
| Species | Amycolatopsis azurea |
| Txid | 36819 |
| 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 | C29H42N4O6 → C29H42N4O7 |
| Reaction Type | Oxidation |
| Chemical Bond | CH |
| Solvents | Water |
| Conditions | 12 h, 30°C |
| Transformations | 1.Hydroxylation of Aromatic Compounds 2.Hydroxylation at an Aromatic Carbon |
Substrate Information:
| Substrate Name | p-Deoxy-AS 1429716 |
| Substrate Chemical Formula | C29H42N4O6 |
| Substrate PubChem CID | 44563351 |
| Substrate Smiles | O=C1N2[C@@](C(=O)N[C@@H](CCCCCC([C@@H](C)O)=O)C(=O)N[C@](CC)(C)C(=O)N[C@H]1CC3=CC=CC=C3)(CCC2)[H] |
| Substrate Structure |
Product Information:
| Product Name | Cyclo[(2S,9R)-2-amino-9-hydroxy-8-oxodecanoyl-L-isovalyl-L-tyrosyl-D-prolyl] |
| Product Chemical Formula | C29H42N4O7 |
| Product PubChem CID | 49871644 |
| Product CAS Number | 561042-39-5 |
| Product Smiles | O=C1N2[C@@](C(=O)N[C@@H](CCCCCC([C@@H](C)O)=O)C(=O)N[C@](CC)(C)C(=O)N[C@H]1CC3=CC=C(O)C=C3)(CCC2)[H] |
| Product Structure |
References:
| Title: | Cloning and heterologous expression of P450Um-1, a novel bacterial P450 gene, for hydroxylation of immunosuppressive agent AS1387392. |
| PMID: | 20924385 |
| Journal: | Journal of Antibiotics |
| Year: | 2010/10/6 |