9HAO

BDM91531 inhibitor bound to the transmembrane domain of AcrB

Summary for 9HAO

• Entry DOI: 10.2210/pdb9hao/pdb
• Related: 8QZQ 8QZT
• Descriptor: Multidrug efflux pump subunit AcrB, [3-(3-chloranyl-2-piperazin-1-yl-quinolin-6-yl)phenyl]methanamine, DECANE, ... (16 entities in total)
• Functional Keywords: rnd multidrug efflux pump, antimicrobial resistance, allosteric inhibitor, intermediate conformational state, transport protein
• Biological source: Escherichia coli K-12; More
• Total number of polymer chains: 5
• Total formula weight: 394706.89

Authors

Mueller, R.T.,Herrmann, A.,Pos, K.M. (deposition date: 2024-11-04, release date: 2025-11-12, Last modification date: 2026-05-20)

Primary citation

Bornsen, C.,Muller, R.T.,Vieira Da Cruz, A.,Jimenez-Castellanos, J.C.,Meurillon, V.,Brandstatter, L.,Lodinsky, E.V.,Athar, M.,Vargiu, A.V.,Hartkoorn, R.C.,Flipo, M.,Frangakis, A.S.,Pos, K.M.
Molecular mechanism of transition-state inhibitors of bacterial antibiotic efflux pumps.
NPJ Antimicrob Resist, 4:-, 2026

PubMed Abstract: In many Gram-negative bacteria such as Escherichia coli and Klebsiella pneumoniae, the AcrAB-TolC efflux pump is central to multidrug resistance. We report the development of BDM91531, a nanomolar pyridylpiperazine inhibitor that potentiates the activity of several antibiotics. Structural analyses by X-ray crystallography and cryo-EM revealed that the divalent cationic BDM91531 binds AcrB through electrostatic interactions with a central role for residues D408 and E947, trapping protomers in an O to L transitional state and blocking the conformational cycling of the trimer. Differential scanning fluorimetry and susceptibility tests confirmed this inhibitory mechanism. Negative charges at the cytoplasmic rim are essential for inhibitor uptake as electrostatic attraction from rim carboxylates, including E947 and D951, facilitates entry. Loss of D951 abolished inhibitor sensitivity, whereas introducing alternative negative charges restored activity. These findings establish BDM91531 as a potent AcrB efflux pump inhibitor and highlight structural determinants for inhibitor access and binding.

PubMed: 42082832
DOI: 10.1038/s44259-026-00207-6

Experimental method

X-RAY DIFFRACTION (1.94 Å)