PXD025573

PXD025573 is an original dataset announced via ProteomeXchange.

Title	Mapping perturbations in the cellular proteome of OCIAD1 and OCIAD2 knockdown U2OS cells.
Description	To gain insight into the function of both OCIAD paralogs, we used untargeted quantitative mass spectrometry to compare the whole-cell proteomes of control U2OS cells, U2OS cells with individual or double OCIAD1/OCIAD2 knockdown, and OCIAD1 knockdown cells in which OCIAD1 expression was reintroduced by lentiviral delivery.
HostingRepository	PRIDE
AnnounceDate	2021-05-14
AnnouncementXML	Submission_2021-05-14_04:14:54.007.xml
DigitalObjectIdentifier
ReviewLevel	Peer-reviewed dataset
DatasetOrigin	Original dataset
RepositorySupport	Unsupported dataset by repository
PrimarySubmitter	Maxence Le Vasseur
SpeciesList	scientific name: Homo sapiens (Human); NCBI TaxID: 9606;
ModificationList	iodoacetamide derivatized residue
Instrument	Orbitrap Fusion Lumos

Revision	Datetime	Status	ChangeLog Entry
0	2021-04-22 23:16:43	ID requested
⏵ 1	2021-05-14 04:14:54	announced

Dataset with its publication pending

submitter keyword: OCIAD1, OCIAD2, knockdown, mitochondria, Complex III, cytochrome c1

Jodi Nunnari
contact affiliation	Department of Molecular and Cellular Biology, College of Biological Sciences, University of California, Davis, CA, 95616, USA
contact email	jmnunnari@ucdavis.edu
lab head
Maxence Le Vasseur
contact affiliation	University of California, Davis
contact email	mlevasseur@ucdavis.edu
dataset submitter

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/2021/05/PXD025573

PRIDE project URI

• PRIDE
  1. PXD025573
     1. Label: PRIDE project
     2. Name: Mapping perturbations in the cellular proteome of OCIAD1 and OCIAD2 knockdown U2OS cells.