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PXD027705-1

PXD027705 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleRegulated biogenesis and targeting of monotopic squalene monooxygenase requires the GET pathway
DescriptionThis study investigated get3 mutant yeast cell. Proteins of the GET pathway are involved in targeting of C-terminally anchored transmembrane proteins and protection against lipotoxicity. Get3 cells revealed an altered ergosterol production and susceptibility towards a sterol synthesis inhibiting drug terbinafine. Furthermore, we identified a member of a non-canonical GET pathway client, a monotopic membrane protein squalene monooxygenase Erg1 that may be responsible for the susceptibility of Get3 mutant to lipotoxic agents.
HostingRepositoryPRIDE
AnnounceDate2022-06-09
AnnouncementXMLSubmission_2022-06-09_07:15:38.776.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterIvan Silbern
SpeciesList scientific name: Saccharomyces cerevisiae (Baker's yeast); NCBI TaxID: 4932;
ModificationListmonohydroxylated residue
InstrumentQ Exactive HF
Dataset History
RevisionDatetimeStatusChangeLog Entry
02021-08-05 04:38:24ID requested
12022-06-09 07:15:39announced
Publication List
Farkas Á, Urlaub H, Bohnsack KE, Schwappach B, Regulated targeting of the monotopic hairpin membrane protein Erg1 requires the GET pathway. J Cell Biol, 221(6):(2022) [pubmed]
Keyword List
submitter keyword: squalene monooxygenase, GET pathway, Get3, Erg1, lipotoxicity, terbinafine, LFQ, in-gel digestion
Contact List
Prof. Dr. Henning Urlaub
contact affiliationBioanalytical Mass Spectrometry Group, Max-Planck Institute for Biophysical Chemistry, Am Fassberg 11, 37077 Goettingen, Germany
contact emailhenning.urlaub@mpibpc.mpg.de
lab head
Ivan Silbern
contact affiliationMPI Biophysical Chemistry
contact emailivansilbern@gmail.com
dataset submitter
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Dataset FTP location
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