9EXV

Broad substrate scope C-C oxidation in cyclodipeptides catalysed by a flavin-dependent filament

9EXV の概要

• エントリーDOI: 10.2210/pdb9exv/pdb
• EMDBエントリー: 50049
• 分子名称: Nitroreductase, AlbB, FLAVIN MONONUCLEOTIDE (3 entities in total)
• 機能のキーワード: cyclodipeptides oxidase, oxidoreductase
• 由来する生物種: Nocardiopsis dassonvillei; 詳細
• タンパク質・核酸の鎖数: 6
• 化学式量合計: 89221.11

構造登録者

Sutherland, E.,Sundaramoorthy, R.,Czekster, C.M. (登録日: 2024-04-08, 公開日: 2025-02-05)

主引用文献

Sutherland, E.,Harding, C.J.,du Monceau de Bergendal, T.,Florence, G.J.,Ackermann, K.,Bode, B.E.,Synowsky, S.,Sundaramoorthy, R.,Czekster, C.M.
Broad substrate scope C-C oxidation in cyclodipeptides catalysed by a flavin-dependent filament.
Nat Commun, 16:995-995, 2025

PubMed Abstract: Cyclic dipeptides are produced by organisms across all domains of life, with many exhibiting anticancer and antimicrobial properties. Oxidations are often key to their biological activities, particularly C-C bond oxidation catalysed by tailoring enzymes including cyclodipeptide oxidases. These flavin-dependent enzymes are underexplored due to their intricate three-dimensional arrangement involving multiple copies of two distinct small subunits, and mechanistic details underlying substrate selection and catalysis are lacking. Here, we determined the structure and mechanism of the cyclodipeptide oxidase from the halophile Nocardiopsis dassonvillei (NdasCDO), a component of the biosynthetic pathway for nocazine natural products. We demonstrated that NdasCDO forms filaments in solution, with a covalently bound flavin mononucleotide (FMN) cofactor at the interface between three distinct subunits. The enzyme exhibits promiscuity, processing various cyclic dipeptides as substrates in a distributive manner. The reaction is optimal at high pH and involves the formation of a radical intermediate. Pre-steady-state kinetics, a significant solvent kinetic isotope effect, and the absence of viscosity effects suggested that a step linked to FMN regeneration controlled the reaction rate. Our work elucidates the complex mechanistic and structural characteristics of this dehydrogenation reaction, positioning NdasCDO as a promising biocatalyst and expanding the FMN-dependent oxidase family to include enzyme filaments.

PubMed: 39856061
DOI: 10.1038/s41467-025-56127-y

実験手法

ELECTRON MICROSCOPY (3 Å)