8STB

The structure of abxF, an enzyme catalyzing the formation of the chiral spiroketal of an anthrabenzoxocinone antibiotic, (-)-ABX

8STB の概要

• エントリーDOI: 10.2210/pdb8stb/pdb
• 分子名称: Glyoxalase, SULFATE ION, GLYCEROL, ... (5 entities in total)
• 機能のキーワード: diels-alderase, biosynthesis, antibiotics, chiral spiroketal, biosynthetic protein
• 由来する生物種: Streptomyces sp.
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 48310.36

構造登録者

Luo, Z.,Jia, X.,Yan, X.,Qu, X.,Kobe, B. (登録日: 2023-05-09, 公開日: 2024-05-22, 最終更新日: 2025-06-04)

主引用文献

Yan, X.,Jia, X.,Luo, Z.,Ji, S.,Zhang, M.J.,Zhang, H.,Yu, M.,Orts, J.,Jiang, K.,Lin, Z.,Deng, Z.,Kong, X.D.,Kobe, B.,Zhao, Y.L.,Mobli, M.,Qu, X.
An enzymatic dual-oxa Diels-Alder reaction constructs the oxygen-bridged tricyclic acetal unit of (-)-anthrabenzoxocinone.
Nat.Chem., 2025

PubMed Abstract: The hetero-Diels-Alder (HDA) reaction is a key method for synthesizing six-membered heterocyclic rings in natural products and bioactive compounds. Despite its importance in synthetic chemistry, naturally occurring enzymatic HDA reactions are rare and limited to a single heteroatom. Here we report AbxF, a bifunctional vicinal oxygen chelate (VOC)-like protein that catalyses dehydration and dual-oxa Diels-Alder reactions to stereoselectively form the oxygen-bridged tricyclic acetal of (-)-anthrabenzoxocinone ((-)-ABX). Isotope assays and density functional theory calculations reveal a dehydration-coordinated, concerted HDA mechanism. The crystal structure of AbxF and NMR complex structures of AbxF with its substrate analogue and (-)-ABX define the reaction's structural basis. Mutational analysis identifies Asp17 as a general base that mediates dehydration, forming an o-quinone methide intermediate for stereoselective dual-oxa HDA. This work establishes the molecular and structural basis of a polyheteroatomic Diels-Alderase, paving the way for designing polyheteroatomic DA enzymatic tools.

PubMed: 40263633
DOI: 10.1038/s41557-025-01804-0

実験手法

X-RAY DIFFRACTION (2.22 Å)