PXD059917 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Characterisation of BiP-GRP94-HT2 interaction |
Description | Characterization of the interaction of BiP-GRP94 in the presence and absence of HT2 using cross linking with DSBU and subsequent analysis of cross linked peptides by LC-MS/MS |
HostingRepository | PRIDE |
AnnounceDate | 2025-07-14 |
AnnouncementXML | Submission_2025-07-14_05:47:08.903.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Farnusch Kaschani |
SpeciesList | scientific name: Mus musculus (Mouse); NCBI TaxID: 10090; |
ModificationList | monohydroxylated residue; iodoacetamide derivatized residue |
Instrument | Orbitrap Fusion Lumos |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2025-01-17 05:59:12 | ID requested | |
⏵ 1 | 2025-07-14 05:47:09 | announced | |
Publication List
Dataset with its publication pending |
Keyword List
submitter keyword: BiP |
GRP94 |
cross linking MS |
CL-MS |
DSBU |
Contact List
Farnusch Kaschani |
contact affiliation | Analytics Core Facility Essen (ACE), Chemische Biologie, Universität Duisburg-Essen, ZMB, Germany |
contact email | farnusch.kaschani@uni-due.de |
lab head | |
Farnusch Kaschani |
contact affiliation | University Duisburg-Essen |
contact email | farnusch.kaschani@uni-due.de |
dataset submitter | |
Full Dataset Link List
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/2025/07/PXD059917 |
PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD059917
- Label: PRIDE project
- Name: Characterisation of BiP-GRP94-HT2 interaction