6PML

Crystal Structure of EcDsbA in complex benzyl ether 23

6PML の概要

• エントリーDOI: 10.2210/pdb6pml/pdb
• 分子名称: Thiol:disulfide interchange protein DsbA, DI(HYDROXYETHYL)ETHER, [6-(benzyloxy)-1-benzofuran-3-yl]acetic acid, ... (5 entities in total)
• 機能のキーワード: disulfide oxidoreductase, redox protein, oxidoreductase-inhibitor complex, oxidoreductase, oxidoreductase/inhibitor
• 由来する生物種: Escherichia coli (strain K12)
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 42762.01

構造登録者

Ilyichova, O.V.,Scanlon, M.J. (登録日: 2019-07-02, 公開日: 2019-11-06, 最終更新日: 2024-10-23)

主引用文献

Duncan, L.F.,Wang, G.,Ilyichova, O.V.,Scanlon, M.J.,Heras, B.,Abbott, B.M.
The Fragment-Based Development of a Benzofuran Hit as a New Class of Escherichia coli DsbA Inhibitors.
Molecules, 24:-, 2019

PubMed Abstract: A fragment-based drug discovery approach was taken to target the thiol-disulfide oxidoreductase enzyme DsbA from (DsbA). This enzyme is critical for the correct folding of virulence factors in many pathogenic Gram-negative bacteria, and small molecule inhibitors can potentially be developed as anti-virulence compounds. Biophysical screening of a library of fragments identified several classes of fragments with affinity to DsbA. One hit with high mM affinity, 2-(6-bromobenzofuran-3-yl)acetic acid (), was chemically elaborated at several positions around the scaffold. X-ray crystal structures of the elaborated analogues showed binding in the hydrophobic binding groove adjacent to the catalytic disulfide bond of DsbA. Binding affinity was calculated based on NMR studies and compounds and were identified as the highest affinity binders with dissociation constants () of 326 ± 25 and 341 ± 57 µM respectively. This work suggests the potential to develop benzofuran fragments into a novel class of DsbA inhibitors.

PubMed: 31635355
DOI: 10.3390/molecules24203756

実験手法

X-RAY DIFFRACTION (2 Å)