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 | C88H99Cl2N9O33 → C88H97Cl2N9O33 |
| Reaction Type | Oxidation |
| Chemical Bond | C-C |
OxyC
Substrate Information:
| Substrate Name | / |
| Substrate Chemical Formula | C88H99Cl2N9O33 |
| Substrate Smiles | CCCCCCCCCC(N[C@H]1[C@H](OC2=C3OC4C=CC([C@@H](O[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5NC(C)=O)[C@H](NC(=O)[C@H](NC([C@H]5C(=C3)C=C2OC2C=CC(=CC=2Cl)C[C@@H]2C(N[C@@H](C3C=C(OC6C=C([C@@H](N)C(N2)=O)C=CC=6O)C=C(O)C=3)C(=O)N5)=O)=O)C2=CC=C(O)C=C2)C(N[C@H](C(O)=O)C2C=C(O)C=C(OC3O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]3O)C=2)=O)=CC=4Cl)O[C@H](CO)[C@@H](O)[C@@H]1O)=O |
| Substrate Structure |
Product Information:
| Product Name | Teicoplanin |
| Product Chemical Formula | C88H97Cl2N9O33 |
| Product PubChem CID | 133065662 |
| Product CAS Number | 61036-62-2 |
| Product Smiles | CCCCCCCCCC(=O)N[C@@H]1[C@H]([C@@H]([C@H](O[C@H]1OC2=C3C=C4C=C2OC5=C(C=C(C=C5)[C@H]([C@H]6C(=O)N[C@@H](C7=C(C(=CC(=C7)O)OC8[C@H]([C@H]([C@@H]([C@H](O8)CO)O)O)O)C9=C(C=CC(=C9)[C@H](C(=O)N6)NC(=O)[C@@H]4NC(=O)[C@@H]1C2=CC(=CC(=C2)OC2=C(C=CC(=C2)[C@H](C(=O)N[C@H](CC2=CC(=C(O3)C=C2)Cl)C(=O)N1)N)O)O)O)C(=O)O)O[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)NC(=O)C)Cl)CO)O)O |
| Product Structure |
References:
| Title: | Radical enzymatic peptide cyclization in natural product biosynthesis |
| PMID: | 41697225 |
| Journal: | Chemical Society reviews |
| Year: | 2026/3/9 |