8TTH

NorA single mutant - D307N at pH 7.5

8TTH の概要

• エントリーDOI: 10.2210/pdb8tth/pdb
• EMDBエントリー: 41605 41606 41607 41608
• 分子名称: Quinolone resistance protein NorA, Heavy Chain of FabDA1 Variable Domain, Light Chain of FabDA1 Variable Domain (3 entities in total)
• 機能のキーワード: d307n nora, efflux pump, mrsa, transport protein, transport protein-immune system complex, transport protein/immune system
• 由来する生物種: Staphylococcus aureus; 詳細
• タンパク質・核酸の鎖数: 3
• 化学式量合計: 71934.88

構造登録者

Li, J.P.,Li, Y.,Koide, A.,Kuang, H.H.,Torres, V.J.,Koide, S.,Wang, D.N.,Traaseth, N.J. (登録日: 2023-08-13, 公開日: 2024-05-29, 最終更新日: 2025-06-04)

主引用文献

Li, J.,Li, Y.,Koide, A.,Kuang, H.,Torres, V.J.,Koide, S.,Wang, D.N.,Traaseth, N.J.
Proton-coupled transport mechanism of the efflux pump NorA.
Nat Commun, 15:4494-4494, 2024

PubMed Abstract: Efflux pump antiporters confer drug resistance to bacteria by coupling proton import with the expulsion of antibiotics from the cytoplasm. Despite efforts there remains a lack of understanding as to how acid/base chemistry drives drug efflux. Here, we uncover the proton-coupling mechanism of the Staphylococcus aureus efflux pump NorA by elucidating structures in various protonation states of two essential acidic residues using cryo-EM. Protonation of Glu222 and Asp307 within the C-terminal domain stabilized the inward-occluded conformation by forming hydrogen bonds between the acidic residues and a single helix within the N-terminal domain responsible for occluding the substrate binding pocket. Remarkably, deprotonation of both Glu222 and Asp307 is needed to release interdomain tethering interactions, leading to opening of the pocket for antibiotic entry. Hence, the two acidic residues serve as a "belt and suspenders" protection mechanism to prevent simultaneous binding of protons and drug that enforce NorA coupling stoichiometry and confer antibiotic resistance.

PubMed: 38802368
DOI: 10.1038/s41467-024-48759-3

実験手法

ELECTRON MICROSCOPY (3.54 Å)