PXD041359 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Conformational restriction shapes the inhibition of a multidrug efflux adaptor protein |
Description | Membrane efflux pumps play a major role in bacterial multidrug resistance. The tripartite multidrug efflux pump system from Escherichia coli, AcrAB-TolC, is a target for inhibition to lessen resistance development and restore antibiotic efficacy, with homologs in other ESKAPE pathogens. Here, we rationalize a mechanism of inhibition against the periplasmic adaptor protein, AcrA, using a combination of hydrogen/deuterium exchange mass spectrometry, cellular efflux assays, and molecular dynamics simulations. We define the structural dynamics of AcrA and find that an inhibitor can inflict long-range stabilisation across all four of its domains, whereas an interacting efflux substrate has minimal effect. Our results support a model where an inhibitor forms a molecular wedge within a cleft between the lipoyl and αβ domains of AcrA, diminishing its conformational transmission of drug-evoked signals from AcrB to TolC. This work provides molecular insights into multidrug adaptor protein function which could be valuable for developing antimicrobial therapeutics. |
HostingRepository | PRIDE |
AnnounceDate | 2023-06-01 |
AnnouncementXML | Submission_2023-06-01_07:07:46.142.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | BenjaminRussell Lewis |
SpeciesList | scientific name: Escherichia coli; NCBI TaxID: 562; |
ModificationList | No PTMs are included in the dataset |
Instrument | Q Exactive HF; SYNAPT G2-Si; Xevo G2-XS QTof |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2023-04-05 15:12:47 | ID requested | |
⏵ 1 | 2023-06-01 07:07:46 | announced | |
2 | 2024-10-22 05:46:12 | announced | 2024-10-22: Updated project metadata. |
Publication List
Dataset with its publication pending |
Keyword List
submitter keyword: Membrane proteins,Multidrug efflux pump, Efflux pump inhibitors, HDX-MS |
Contact List
EamonnReading |
contact affiliation | Department of Chemisty, Redaing Group, King's College London |
contact email | eamonn.reading@kcl.ac.uk |
lab head | |
BenjaminRussell Lewis |
contact affiliation | King's College London |
contact email | benjamin.russell_lewis@kcl.ac.uk |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/06/PXD041359 |
PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD041359
- Label: PRIDE project
- Name: Conformational restriction shapes the inhibition of a multidrug efflux adaptor protein