PXD014936 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Complexome profiling of mitochondrial protein complexes from patients with mutation in NDUFC2 gene |
Description | NDUFC2 is a subunit of the membrane part of NADH:ubiquinone oxidoreductase (complex I). Here we used complexome profiling to study the role of NDUFC2 in complex I stability and assembly. |
HostingRepository | PRIDE |
AnnounceDate | 2020-08-10 |
AnnouncementXML | Submission_2020-08-10_04:30:00.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Ilka Wittig |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | iodoacetamide derivatized residue |
Instrument | Q Exactive |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2019-08-08 01:41:06 | ID requested | |
⏵ 1 | 2020-08-10 04:30:00 | announced | |
2 | 2020-09-29 23:29:07 | announced | 2020-09-30: Updated publication reference for PubMed record(s): 32969598. |
3 | 2024-10-22 05:10:30 | announced | 2024-10-22: Updated project metadata. |
Publication List
Dataset with its publication pending |
Keyword List
submitter keyword: LC-MSMS, complexome profiling, oxidative phosphorylation system, complex I assembly |
Contact List
Robert Taylor |
contact affiliation | (Head, NHS Highly Specialised Mitochondrial Diagnostic Laboratory and Professor of Mitochondrial Pathology), Wellcome Centre for Mitochondrial Research, Newcastle University, UK |
contact email | robert.taylor@ncl.ac.uk |
lab head | |
Ilka Wittig |
contact affiliation | Functional Proteomics, Goethe University, Frankfurt am Main , Germany |
contact email | wittig@med.uni-frankfurt.de |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD014936
- Label: PRIDE project
- Name: Complexome profiling of mitochondrial protein complexes from patients with mutation in NDUFC2 gene