9KUS
Cryo-EM structure of C-Methyltransferase from Rhododendron dauricum
9KUS の概要
| エントリーDOI | 10.2210/pdb9kus/pdb |
| EMDBエントリー | 62579 |
| 分子名称 | C-Methyltransferase from Rhododendron dauricum (1 entity in total) |
| 機能のキーワード | methyltransferase, dimer, transferase |
| 由来する生物種 | Rhododendron dauricum |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 86223.17 |
| 構造登録者 | |
| 主引用文献 | Zhang, M.,Bao, Y.O.,Dai, Z.,Qian, Z.,Yu, H.,Zhou, J.J.,Chen, Y.,Wang, Z.,Wang, K.,Cai, M.,Ye, M. Molecular and Structural Characterization of a Chalcone di- C -Methyltransferase RdCMT from Rhododendron dauricum and Its Application in De Novo Biosynthesis of Farrerol in Pichia pastoris . J.Am.Chem.Soc., 147:17132-17143, 2025 Cited by PubMed Abstract: Methylation plays a crucial role in drug design and optimization. While numerous methyltransferases have been characterized from plants, -methyltransferases, particularly those targeting phenolic skeletons, are rare. In this study, we identified a novel di--methyltransferase RdCMT from the medicinal plant . RdCMT catalyzes a sequential two-step 3'-/5'--methylation of naringenin chalcone, leading to the biosynthesis of farrerol. RdCMT exhibited a strict substrate specificity for chalcones. Through combinatorial catalysis, a series of -methylated flavonoids were synthesized. Moreover, farrerol was synthesized de novo in and with yields of 0.4 mg/g (dry weight) and 149.0 mg/L, respectively. The structure of RdCMT was determined using cryo-electron microscopy (cryo-EM), revealing that residues R328 and G296 significantly influence the substrate specificity of RdCMT. This work not only introduces a potent biocatalyst for the preparation of -methylated flavonoids but also offers insights into the catalytic mechanisms of -methyltransferases. PubMed: 40331654DOI: 10.1021/jacs.5c02654 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (3.42 Å) |
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