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PXD028798

PXD028798 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleAnalysis of proteins that bind promoter of the PDR5 multidrug transporter gene in Saccharomyces cerevisiae using minichromosome isolation and LC-MS/MS
DescriptionThe Pleiotropic Drug Resistance (PDR) network is central to the drug response in fungi, and its overactivation is associated with drug resistance. However, gene regulation of the PDR network is not well understood. Here, we established a method to identify proteins that bind promoter of the PDR5 multidrug transporter gene in Saccharomyces cerevisiae using minichromosome isolation and SILAC-based quantitative proteomics, and identified the SWI/SNF chromatin remodelling complex as a PDR5 promoter-binding complex. We also purified the SWI/SNF complex from S. cerevisiae by immunoprecipitating Flag-tagged Snf6, a subunit of SWI/SNF, and identified the subunits of SWI/SNF and its binding proteins by LC-MS/MS.
HostingRepositoryPRIDE
AnnounceDate2022-02-22
AnnouncementXMLSubmission_2022-02-22_02:35:35.047.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterDavid Stead
SpeciesList scientific name: Saccharomyces cerevisiae (Baker's yeast); NCBI TaxID: 4932;
ModificationListiodoacetamide derivatized residue
InstrumentQ Exactive
Dataset History
RevisionDatetimeStatusChangeLog Entry
02021-09-28 03:07:42ID requested
12022-02-22 02:35:35announced
Publication List
Dataset with its publication pending
Keyword List
submitter keyword: Saccharomyces cerevisiae, minichromosome, promoter-binding proteins, immunoprecipitation, LC-MSMS
Contact List
Takashi Kubota
contact affiliationInstitute of Medical Sciences University of Aberdeen Foresterhill Aberdeen AB25 2ZD Scotland UK
contact emailt.kubota@abdn.ac.uk
lab head
David Stead
contact affiliationUniversity of Aberdeen
contact emaild.stead@abdn.ac.uk
dataset submitter
Full Dataset Link List
Dataset FTP location
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PRIDE project URI
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