9KPU の概要
| エントリーDOI | 10.2210/pdb9kpu/pdb |
| 分子名称 | Cytochrome P450, PROTOPORPHYRIN IX CONTAINING FE, forazoline C, ... (4 entities in total) |
| 機能のキーワード | p450 oxidoreductase, oxidoreductase |
| 由来する生物種 | Actinomadura sp. |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 86896.76 |
| 構造登録者 | |
| 主引用文献 | Chen, X.,Zhang, Y.,Li, S.,Liao, W.,Tao, W.,Deng, Z.,Bugni, T.S.,Su, H.,Zhang, F. Cytochrome P450 Mediated Cyclohexane Ring Formation in Forazoline Biosynthesis. Angew.Chem.Int.Ed.Engl., :e202504925-e202504925, 2025 Cited by PubMed Abstract: Forazoline A, produced by the marine actinomycete Actinomadura sp. WMMB-499, is a unique PK/NRP hybrid macrolactone with promising antifungal in vivo efficacy through a previously unreported mechanism. Although a PKS/NRPS gene cluster was identified as a candidate for forazoline production, the precise biosynthetic pathway and the functions of the tailoring enzymes remain unclear. In this work, the functions of three cytochrome P450 mono-oxygenases (FrazP1P2P3) were characterized. Notably, FrazP2 was found to mediate cyclohexane ring formation from an 1,3,6-triene precursor during forazoline A biosynthesis, as confirmed by genetic and biochemical analysis. To gain structural and mechanistic insight into the activity of FrazP2, the crystal structure of a FrazP2-substrate complex has been solved at 2.3 Å resolution. The molecular dynamics simulations and DFT calculations revealed an unprecedented enzyme-catalyzed oxidative cyclization reaction by FrazP2. These findings expand our understanding of the catalytic diversity of cytochrome P450s, contributing to the diversification of natural products and enabling the creation of unnatural derivatives with increased antifungal potency. PubMed: 40329414DOI: 10.1002/anie.202504925 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.3 Å) |
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