8STB
The structure of abxF, an enzyme catalyzing the formation of the chiral spiroketal of an anthrabenzoxocinone antibiotic, (-)-ABX
Summary for 8STB
| Entry DOI | 10.2210/pdb8stb/pdb |
| Descriptor | Glyoxalase, SULFATE ION, GLYCEROL, ... (5 entities in total) |
| Functional Keywords | diels-alderase, biosynthesis, antibiotics, chiral spiroketal, biosynthetic protein |
| Biological source | Streptomyces sp. |
| Total number of polymer chains | 2 |
| Total formula weight | 48310.36 |
| Authors | |
| Primary citation | 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 Cited by 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: 40263633DOI: 10.1038/s41557-025-01804-0 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.22 Å) |
Structure validation
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