P450 Protein:
| P450 Symbol | OxyC |
| Protein Name | OxyC |
| Uniprot ID | A0A385L3H7 |
| Species | Amycolatopsis keratiniphila |
| Txid | 129921 |
| 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 | C66H75ClN8O24 → C66H75Cl2N9O24 |
| Reaction Type | Oxidation |
| Chemical Bond | C-C |
OxyC
Substrate Information:
| Substrate Name | / |
| Substrate Chemical Formula | C66H75ClN8O24 |
| Substrate Smiles | C1C=C([C@H](NC(=O)[C@@H]2[C@H](O)C3=CC=C(C(=C3)Cl)OC3=CC4=CC(OC5=C([*])C=C(C=C5)[C@@H](O)[C@@H](NC([C@H](NC)CC(C)C)=O)C(=O)N[C@@H](CC(=O)N)C(=O)N[C@H]4C(=O)N[C@H](C4C=CC(O)=CC=4)C(=O)N2)=C3O[C@H]2C(C(O)C(O)[C@@H](CO)O2)O[C@@H]2CC(C)([*])C(O)[C@H](C)O2)C(=O)O)C(O)=CC=1O |
| Substrate Structure |
Product Information:
| Product Name | Vancomycin |
| Product Chemical Formula | C66H75Cl2N9O24 |
| Product PubChem CID | 14969 |
| Product CAS Number | 1404-90-6 |
| Product Smiles | C[C@H]1[C@H]([C@@](C[C@@H](O1)O[C@@H]2[C@H]([C@@H]([C@H](O[C@H]2OC3=C4C=C5C=C3OC6=C(C=C(C=C6)[C@H]([C@H](C(=O)N[C@H](C(=O)N[C@H]5C(=O)N[C@@H]7C8=CC(=C(C=C8)O)C9=C(C=C(C=C9O)O)[C@H](NC(=O)[C@H]([C@@H](C1=CC(=C(O4)C=C1)Cl)O)NC7=O)C(=O)O)CC(=O)N)NC(=O)[C@@H](CC(C)C)NC)O)Cl)CO)O)O)(C)N)O |
| Product Structure |
References:
| Title: | Radical enzymatic peptide cyclization in natural product biosynthesis |
| PMID: | 41697225 |
| Journal: | Chemical Society reviews |
| Year: | 2026/3/9 |