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9CUS

BmrCD in the outward-facing conformation bound to Hoechsts

Summary for 9CUS
Entry DOI10.2210/pdb9cus/pdb
Related8FMV 8T1P
EMDB information29297 40974 45940
DescriptorProbable multidrug resistance ABC transporter ATP-binding/permease protein YheI, Probable multidrug resistance ABC transporter ATP-binding/permease protein YheH, MAGNESIUM ION, ... (7 entities in total)
Functional Keywordsabc transporter, exporter, membrane protein, transport
Biological sourceBacillus subtilis subsp. subtilis str. 168
More
Total number of polymer chains2
Total formula weight162263.57
Authors
Tang, Q.,Mchaourab, H.S. (deposition date: 2024-07-26, release date: 2025-08-13, Last modification date: 2025-09-03)
Primary citationTang, Q.,Sinclair, M.,Bisignano, P.,Zhang, Y.,Tajkhorshid, E.,Mchaourab, H.S.
Lipid-mediated mechanism of drug extrusion by a heterodimeric ABC exporter.
Biorxiv, 2025
Cited by
PubMed Abstract: Multidrug transport by ATP binding cassette (ABC) exporters entails a mechanism to modulate drug affinity across the transport cycle. Here, we combine cryo-EM and molecular dynamics (MD) simulations to illuminate how lipid competition modulates substrate affinity to drive its translocation by ABC exporters. We determined cryo-EM structures of the ABC transporter BmrCD in drug-loaded inward-facing (IF) and outward-facing (OF) conformations in lipid nanodiscs to reveal the structural basis of alternating access, details of drug-transporter interactions, and the scale of drug movement between the two conformations. Remarkably, the structures uncovered lipid molecules bound in or near the transporter vestibule along with the drugs. MD trajectories from the IF structure show that these lipids stimulate drug disorder and translocation towards the vestibule apex. Similarly, bound lipids enter the OF vestibule and weaken drug-transporter interactions facilitating drug release. Our results complete a near-atomic model of BmrCD's conformational cycle and advance a general mechanism of lipid-driven drug transport by ABC exporters.
PubMed: 40060395
DOI: 10.1101/2025.02.26.640354
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.1 Å)
Structure validation

242500

数据于2025-10-01公开中

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