8ZLS

Apo structure of BBE-like oxidative cyclase MaDS1

8ZLS の概要

• エントリーDOI: 10.2210/pdb8zls/pdb
• 分子名称: MaDS1, FLAVIN-ADENINE DINUCLEOTIDE (3 entities in total)
• 機能のキーワード: bbe-like enzyme, oxidative cyclase, flavoprotein, plant protein
• 由来する生物種: Morus alba
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 119419.69

構造登録者

Guo, N.,Fan, J.,Yang, J.,Lei, X. (登録日: 2024-05-21, 公開日: 2025-08-13, 最終更新日: 2025-09-03)

主引用文献

Guo, N.,Gu, J.,Zhou, Q.,Liu, F.,Dong, H.,Ding, Q.,Wang, Q.,Wu, D.,Yang, J.,Fan, J.,Gao, L.,Houk, K.N.,Lei, X.
Aspartic acid residues in BBE-like enzymes from Morus alba promote a function shift from oxidative cyclization to dehydrogenation.
Proc.Natl.Acad.Sci.USA, 122:e2504346122-e2504346122, 2025

PubMed Abstract: Berberine bridge enzyme (BBE)-like enzymes catalyze various oxidative cyclization and dehydrogenation reactions in natural product biosynthesis, but the molecular mechanism underlying the selectivity remains unknown. Here, we elucidated the catalytic mechanism of BBE-like oxidases from involved in the oxidative cyclization and dehydrogenation of moracin C. X-ray crystal structures of a functionally promiscuous flavin adenine dinucleotide (FAD)-bound oxidase, MaDS1, with and without an oxidative dehydrogenation product were determined at 2.03 Å and 2.21 Å resolution, respectively. Structure-guided mutagenesis and sequence analysis have identified a conserved aspartic acid that directs the reaction toward the oxidative dehydrogenation pathway. A combination of density functional theory (DFT) calculations and molecular dynamics (MD) simulations has revealed that aspartic acid acts as the catalytic base to deprotonate the carbon-cation intermediate to generate the dehydrogenated product, which otherwise undergoes a spontaneous 6π electrocyclization in the oxidative cyclization pathway to furnish the 2H-benzopyran product.

PubMed: 40828030
DOI: 10.1073/pnas.2504346122

実験手法

X-RAY DIFFRACTION (2.21 Å)