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PXD015333-1

PXD015333 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleThe anti-MRSA compound KCR inhibits protein synthesis in Staphylococcus aureus
DescriptionS aureus was treated in triplicate with 3-O-alpha-L-(2",3"-di-p-coumaroyl)rhamnoside (KCR), oxacillin or vehicle and quantitative proteomic analysis was carried out using isobaric tags and mass spectrometry. 1190 proteins were identified and 552 were affected by KCR (q<0.01). Ontology analysis identified 6 distinct translation-related categories that were affected by KCR (PIANO, 10% false-discovery rate) including structural constituent of ribosome, translation, rRNA binding, tRNA binding, tRNA processing and aminoacyl-tRNA ligase activity. Median fold changes (KCR vs Control) for small and large ribosomal components were 1.46 and 1.43 respectively.
HostingRepositoryMassIVE
AnnounceDate2022-07-12
AnnouncementXMLSubmission_2022-07-12_12:31:32.276.xml
DigitalObjectIdentifier
ReviewLevelNon peer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportSupported dataset by repository
PrimarySubmitterNick Carruthers
SpeciesList scientific name: Staphylococcus aureus; NCBI TaxID: 1280;
ModificationListL-methionine sulfoxide; S-carboxamidomethyl-L-cysteine
InstrumentQ Exactive
Dataset History
RevisionDatetimeStatusChangeLog Entry
02019-09-05 07:56:50ID requested
12022-07-12 12:31:32announced
Publication List
no publication
Keyword List
submitter keyword: methicillin-resistant, Staphylococcus aureus, 3-O-alpha-L-(2",3"-di-p-coumaroyl)rhamnoside, KCR, proteomics, isobaric tags, mechanism of action
Contact List
Nicholas Carruthers
contact affiliationWayne State University
contact emailcarruthers@wayne.edu
lab head
Nick Carruthers
contact affiliationWayne State U
contact emailcarruthers@wayne.edu
dataset submitter
Full Dataset Link List
MassIVE dataset URI
Dataset FTP location
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