6KA2
Crystal structure of a Thebaine synthase from Papaver somniferum in complex with TBN
6KA2 の概要
| エントリーDOI | 10.2210/pdb6ka2/pdb |
| 分子名称 | Thebaine synthase 2, (4R,7aR,12bS)-7,9-dimethoxy-3-methyl-2,4,7a,13-tetrahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline (3 entities in total) |
| 機能のキーワード | synthase, crystallization, biosynthetic protein |
| 由来する生物種 | Papaver somniferum (Opium poppy) |
| タンパク質・核酸の鎖数 | 4 |
| 化学式量合計 | 73299.26 |
| 構造登録者 | Xue, J.,Yu, X.J.,Huang, J.W.,Liu, W.D.,Chen, C.C.,Guo, R.T. (登録日: 2019-06-20, 公開日: 2020-06-24, 最終更新日: 2023-11-22) |
| 主引用文献 | Chen, C.C.,Xue, J.,Peng, W.,Wang, B.,Zhang, L.,Liu, W.,Ko, T.P.,Huang, J.W.,Zhou, S.,Min, J.,Ma, L.,Dai, L.,Guo, R.T.,Yu, X. Structural insights into thebaine synthase 2 catalysis. Biochem.Biophys.Res.Commun., 529:156-161, 2020 Cited by PubMed Abstract: Thebaine synthase 2 (THS2) that can transform (7S)-salutaridinol 7-O-acetate to thebaine catalyzes the final step of thebaine biosynthesis in Papaver somniferum. Here, the crystal structures of THS2 and its complex with thebaine are reported, revealing the interaction network in the substrate-binding pocket. Subsequent docking and QM/MM studies was performed to further explore the catalytic mechanism of THS2. Our results suggest that T105 may abstract the proton of C4-OH from the substrate under the assistance of H89. The resulting C4-O phenolate anion then attacks the nearby C5, and triggers intramolecular S2' syn displacement with the elimination of O-acetyl group. Moreover, the latter S2' reaction is the rate-determining step of the whole enzymatic reaction with an overall energy barrier of 18.8 kcal/mol. These findings are of pivotal importance to understand the mechanism of action of thebaine biosynthesis, and would guide enzyme engineering to enhance the production of opiate alkaloids via metabolic engineering. PubMed: 32703404DOI: 10.1016/j.bbrc.2020.05.199 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.35 Å) |
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