7WDH
Crystal structure of the P450 BM3 heme domain mutant F87A in complex with N-imidazolyl-hexanoyl-L-phenylalanine, phenol and hydroxylamine
7WDH の概要
| エントリーDOI | 10.2210/pdb7wdh/pdb |
| 分子名称 | Bifunctional cytochrome P450/NADPH--P450 reductase, PROTOPORPHYRIN IX CONTAINING FE, HYDROXYAMINE, ... (6 entities in total) |
| 機能のキーワード | dual-functional small molecule, p450 heme domain, complex, oxidoreductase |
| 由来する生物種 | Priestia megaterium |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 109980.90 |
| 構造登録者 | |
| 主引用文献 | Wang, X.,Lin, X.,Jiang, Y.,Qin, X.,Ma, N.,Yao, F.,Dong, S.,Liu, C.,Feng, Y.,Jin, L.,Xian, M.,Cong, Z. Engineering Cytochrome P450BM3 Enzymes for Direct Nitration of Unsaturated Hydrocarbons. Angew.Chem.Int.Ed.Engl., 62:e202217678-e202217678, 2023 Cited by PubMed Abstract: Applications of the peroxidase activity of cytochrome P450 enzymes in synthetic chemistry remain largely unexplored. We present herein a protein engineering strategy to increase cytochrome P450BM3 peroxidase activity for the direct nitration of aromatic compounds and terminal aryl-substituted olefins in the presence of a dual-functional small molecule (DFSM). Site-directed mutations of key active-site residues allowed the efficient regulation of steric effects to limit substrate access and, thus, a significant decrease in monooxygenation activity and increase in peroxidase activity. Nitration of several phenol and aniline compounds also yielded ortho- and para-nitration products with moderate-to-high total turnover numbers. Besides direct aromatic nitration by P450 variants using nitrite as a nitrating agent, we also demonstrated the use of the DFSM-facilitated P450 peroxidase system for the nitration of the vinyl group of styrene and its derivatives. PubMed: 36660956DOI: 10.1002/anie.202217678 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.68 Å) |
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