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ProteomicsC2C12 myoblast WT vs ETFDH-ko TMT
ETFDH (electron transfer flavoprotein ubiquinone oxidoreductase) is a 64 kDa protein monomer located in the inner mitochondrial membrane, in charge of transferring the electrons received from the electron transfer flavoprotein ETF to the Coenzyme Q (Q). Pathological mutations in ETFDH lead to Multip...
ORGANISM(S): Mus musculus (Mouse) 
2023-10-24 | PXD041825 | Pride
Mouse Myoblast Tmt Etfdh C2c12 
ProteomicsAntimycin A-treated vs ETFDH-ko myoblasts TMT
The electron transfer flavoprotein dehydrogenase (ETFDH) is the bottleneck enzyme of fatty acid oxidation (FAO). We performed a TMT 6plex analysis on Antimycin A treated and ETFDH-ko myoblasts (compared to CRL).
ORGANISM(S): Mus musculus (Mouse) 
2023-10-24 | PXD045588 | Pride
Myoblast Tmt Etfdh Antimycin a 
ProteomicsETFDH, CIII and COQ2 common interactome
Proteomic analysis of the immunocapture (IP) of COQ2, ETFDH and UQCRC2 in skeletal muscle extracts, searching for common interactors Coenzyme Q (Q) is a key lipid electron transporter, but several aspects of its biosynthesis and redox homeostasis remain undefined. Various flavoproteins reduce the Q;...
ORGANISM(S): Mus musculus (Mouse) 
2023-10-24 | PXD045351 | Pride
Etfdh  coenzyme q  oxphos-complex iii  skeletal muscle 
ProteomicsETFDH comigrates with CIII in BN-PAGE
Proteomic analysis of 13 bands from BN-PAGE immunostaining of mouse skeletal muscle mitochondrial proteins: Coenzyme Q (Q) is a key lipid electron transporter, but several aspects of its biosynthesis and redox homeostasis remain undefined. Various flavoproteins reduce the Q; however, in eukaryotes, ...
ORGANISM(S): Mus musculus (Mouse) 
2023-10-24 | PXD045352 | Pride
Coenzyme q  oxphos-complex iii  skeletal muscle  mitochondria 
UnknownAn ETFDH-driven metabolon supports OXPHOS efficiency in skeletal muscle by regulating coenzyme Q homeostasis.
Not available
S-EPMC10896730 | biostudies-literature
UnknownCharacterization of two ETFDH mutations in a novel case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.
Not available
S-EPMC6234560 | biostudies-literature
UnknownNovel ETFDH mutations in four cases of riboflavin responsive multiple acyl-CoA dehydrogenase deficiency.
Not available
S-EPMC6031868 | biostudies-literature
UnknownIdentification of ETFDH gene c. 487 + 2 T > A pathogenic variant and mechanisms for polycystic kidney in neonatal onset MADD.
Not available
S-EPMC11905708 | biostudies-literature
UnknownCase report: A novel c.1842_1845dup mutation of ETFDH in two Chinese siblings with multiple acyl-CoA dehydrogenase deficiency.
Not available
S-EPMC9845722 | biostudies-literature
UnknownClinical Presentations and Genetic Characteristics of Late-Onset MADD Due to ETFDH Mutations in Five Patients: A Case Series.
Not available
S-EPMC8606537 | biostudies-literature
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