PXD014585-1

PXD014585 is an original dataset announced via ProteomeXchange.

Title	Endoplasmic Reticulum Chaperones Stabilize Ligand-Receptive MR1 molecules for Efficient Presentation of Metabolite Antigens
Description	Quantitative MS analysis of MR1 GFP immunoprecipates to identify steady-state binding partnets.
HostingRepository	PRIDE
AnnounceDate	2020-09-16
AnnouncementXML	Submission_2020-09-15_23:27:24.xml
DigitalObjectIdentifier
ReviewLevel	Peer-reviewed dataset
DatasetOrigin	Original dataset
RepositorySupport	Unsupported dataset by repository
PrimarySubmitter	Laura Dagley
SpeciesList	scientific name: Homo sapiens (Human); NCBI TaxID: 9606;
ModificationList	monohydroxylated residue; iodoacetamide derivatized residue
Instrument	impact II

Revision	Datetime	Status	ChangeLog Entry
0	2019-07-12 01:19:12	ID requested
⏵ 1	2020-09-15 23:27:24	announced
2	2020-09-27 23:33:37	announced	2020-09-28: Updated publication reference for PubMed record(s): 32958637.
3	2024-10-22 05:12:22	announced	2024-10-22: Updated project metadata.

Dataset with its publication pending

submitter keyword: MAIT cells, MHC, MR1, label-free MS

Hamish E.G. McWilliam
contact affiliation	Postdoctoral research fellow, Department of Microbiology and Immunology, University of Melbourne, Australia
contact email	hamish.mcwilliam@unimelb.edu.au
lab head
Laura Dagley
contact affiliation	WEHI
contact email	dagley.l@wehi.edu.au
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/2020/09/PXD014585

PRIDE project URI

• PRIDE
  1. PXD014585
     1. Label: PRIDE project
     2. Name: Endoplasmic Reticulum Chaperones Stabilize Ligand-Receptive MR1 molecules for Efficient Presentation of Metabolite Antigens