9D28
Crystal structure of (+)-sabinene synthase from Thuja plicata
9D28 の概要
| エントリーDOI | 10.2210/pdb9d28/pdb |
| 分子名称 | Sabinene synthase (2 entities in total) |
| 機能のキーワード | biosynthesis, terpene, cyclization, lyase |
| 由来する生物種 | Thuja plicata (Western red-cedar, Giant arborvitae) |
| タンパク質・核酸の鎖数 | 4 |
| 化学式量合計 | 256465.41 |
| 構造登録者 | |
| 主引用文献 | Gaynes, M.N.,Osika, K.R.,Christianson, D.W. Structure and Function of Sabinene Synthase, a Monoterpene Cyclase That Generates a Highly Strained [3.1.0] Bicyclic Product. Biochemistry, 63:3147-3159, 2024 Cited by PubMed Abstract: Sabinene is a plant natural product with a distinctive strained [3.1.0] bicyclic ring system that is used commercially as a spicy and pine-like fragrance with citrus undertones. This unusual monoterpene has also been studied as an antifungal and anti-inflammatory agent as well as a next-generation biofuel. In order to understand the molecular determinants of [3.1.0] bicyclic ring formation in sabinene biosynthesis, we now report three X-ray crystal structures of sabinene synthase from Western red cedar, (TpSS), with open and partially closed active site conformations at 2.21-2.72 Å resolution. We additionally report the complete biochemical characterization of sabinene synthase, including steady-state kinetics, active site mutagenesis, and product array profiling. The catalytic metal ion requirement is unexpectedly broad for a class I terpene cyclase: optimal catalytic activity was measured using Mn or Co, with more modest activity observed using Mg or Ni. Kinetic parameters were determined for both full-length TpSS and a deletion variant lacking the putative N-terminal plastidial targeting sequence, designated ΔTpSS. Monoterpene product profiles for both indicated similar product arrays independent of the catalytic metal ion used, with sabinene comprising nearly 90% of the total products generated. Site-directed mutagenesis was utilized to probe the function of active site residues, and several mutants yielded altered product arrays. Most notably, the G458A substitution converted ΔTpSS into a high-activity α-pinene synthase. α-Pinene contains a bicyclic [3.1.1] ring system; structural and mechanistic analyses suggest a molecular rationale for the reprogrammed transannulation reaction, leading to the alternative bicyclic product. PubMed: 39527408DOI: 10.1021/acs.biochem.4c00476 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.32 Å) |
構造検証レポート
検証レポート(詳細版)
をダウンロード






