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PXD019826 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleThe mitochondrial transporter SFXN1 is critical for Complex III integrity and cellular metabolism
DescriptionMutations in acylglycerol kinase (AGK) leads to Sengers syndrome, a rare disease characterized by skeletal myopathy, hypertrophic cardiomyopathy, and cataracts. AGK, in vitro, produces lysophosphatidic acid and phosphatidic acid via phosphorylation of monoacylglycerol and diacylglycerol, accordingly. AGK is also a component of the TIM22 import machinery in the inner mitochondrial membrane and, independent of its kinase activity, has been shown to mediate the import of mitochondrial carrier family (SLC25) members. We compared the proteomes of mitochondria from HEK293 WT and AGK KO cells in order to identify additional candidate substrates of the TIM22 translocase that relies on AGK.
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterAkhilesh Pandey
SpeciesList scientific name: Homo sapiens (Human); NCBI TaxID: 9606;
ModificationListiodoacetamide derivatized residue
InstrumentOrbitrap Fusion Lumos
Dataset History
RevisionDatetimeStatusChangeLog Entry
02020-06-16 23:31:41ID requested
12020-06-17 22:24:29announced
Publication List
Dataset with its publication pending
Keyword List
submitter keyword: AGK, Mitochondria
Contact List
Steven Claypool
contact affiliationDepartment of Physiology, Johns Hopkins University School of Medicine, 725 N Wolfe St, Baltimore, Maryland, USA 21205
contact emailsclaypo1@jhmi.edu
lab head
Akhilesh Pandey
contact affiliationDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905
contact emailpandey.akhilesh@mayo.edu
dataset submitter
Full Dataset Link List
Dataset FTP location
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