Gene Ontology annotation through association of InterPro records with GO terms

Annotation inferences using phylogenetic trees

Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt

Gene Ontology annotation based on curation of immunofluorescence data

Electronic Gene Ontology annotations created by ARBA machine learning models

The intraflavin hydrogen bond in human electron transfer flavoprotein modulates redox potentials and may participate in electron transfer.

Phosphoproteome analysis of functional mitochondria isolated from resting human muscle reveals extensive phosphorylation of inner membrane protein complexes and enzymes.

Cochaperone binding to LYR motifs confers specificity of iron sulfur cluster delivery.

Human METTL20 is a mitochondrial lysine methyltransferase that targets the β subunit of electron transfer flavoprotein (ETFβ) and modulates its activity.

∆F508 CFTR interactome remodelling promotes rescue of cystic fibrosis.

Mitochondrial Protein Interaction Mapping Identifies Regulators of Respiratory Chain Function.

A Single Adaptable Cochaperone-Scaffold Complex Delivers Nascent Iron-Sulfur Clusters to Mammalian Respiratory Chain Complexes I-III.

Molecular cloning and nucleotide sequence of cDNAs encoding the alpha-subunit of human electron transfer flavoprotein.

Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.

Quantitative high-confidence human mitochondrial proteome and its dynamics in cellular context.

CFTR interactome mapping using the mammalian membrane two-hybrid high-throughput screening system.

S1P defects cause a new entity of cataract, alopecia, oral mucosal disorder, and psoriasis-like syndrome.

Differential CFTR-Interactome Proximity Labeling Procedures Identify Enrichment in Multiple SLC Transporters.

Biosynthesis of electron transfer flavoprotein in a cell-free system and in cultured human fibroblasts. Defect in the alpha subunit synthesis is a primary lesion in glutaric aciduria type II.

Multimodal cell maps as a foundation for structural and functional genomics.

cDNA cloning and mitochondrial import of the beta-subunit of the human electron-transfer flavoprotein.

Assignment of Etfdh, Etfb, and Etfa to chromosomes 3, 7, and 13: the mouse homologs of genes responsible for glutaric acidemia type II in human.

Three-dimensional structure of human electron transfer flavoprotein to 2.1-A resolution.

Expression and characterization of two pathogenic mutations in human electron transfer flavoprotein.

Reducing equivalents from beta-oxidation of fatty acids transfer to ETF

ETFDH oxidises ETF (reduced) to ETF, reduces CoQ to CoQH2