UBC
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
MYH10
Gene Ontology Biological Process
- ATP catabolic process [ISO]
- actin cytoskeleton organization [IGI]
- actin filament-based movement [ISO]
- actomyosin structure organization [ISO]
- adult heart development [IMP]
- axon guidance [IMP]
- axonogenesis [IMP]
- brain development [IMP]
- cardiac myofibril assembly [IMP]
- cell proliferation [IMP]
- cerebellar Purkinje cell layer development [IMP]
- exocytosis [IMP]
- fourth ventricle development [IMP]
- in utero embryonic development [IMP]
- lateral ventricle development [IMP]
- mitotic cytokinesis [IMP, ISO]
- myofibril assembly [IMP]
- neuromuscular process controlling balance [IMP]
- neuron migration [IMP]
- neuron projection development [IMP]
- nuclear migration [IMP]
- plasma membrane repair [IMP]
- regulation of cell shape [IMP]
- retina development in camera-type eye [IMP]
- substrate-dependent cell migration, cell extension [IMP]
- third ventricle development [IMP]
- ventricular cardiac muscle cell development [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
- actin cytoskeleton [ISO]
- actomyosin [ISO]
- axon [IDA]
- cell cortex [IDA, ISO]
- cleavage furrow [ISO]
- cytoplasm [IDA, ISO]
- dendritic spine [IDA]
- extracellular vesicular exosome [ISO]
- growth cone [IDA]
- midbody [ISO]
- mitochondrion [ISO]
- myosin II complex [IDA, ISO]
- myosin II filament [ISO]
- myosin complex [IDA]
- neuromuscular junction [IDA]
- neuron projection [IDA]
- neuronal cell body [IDA]
- nucleus [ISO]
- plasma membrane [IDA]
- spindle [IDA]
- stress fiber [IDA, IMP, ISO]
Reconstituted Complex
An interaction is inferred between proteins in vitro. This can include proteins in recombinant form or proteins isolated directly from cells with recombinant or purified bait. For example, GST pull-down assays where a GST-tagged protein is first isolated and then used to fish interactors from cell lysates are considered reconstituted complexes (e.g. PUBMED: 14657240, Fig. 4A or PUBMED: 14761940, Fig. 5). This can also include gel-shifts, surface plasmon resonance, isothermal titration calorimetry (ITC) and bio-layer interferometry (BLI) experiments. The bait-hit directionality may not be clear for 2 interacting proteins. In these cases the directionality is up to the discretion of the curator.
Publication
Mfn2 ubiquitination by PINK1/parkin gates the p97-dependent release of ER from mitochondria to drive mitophagy.
Despite their importance as signaling hubs, the function of mitochondria-ER contact sites in mitochondrial quality control pathways remains unexplored. Here we describe a mechanism by which Mfn2, a mitochondria-ER tether, gates the autophagic turnover of mitochondria by PINK1 and parkin. Mitochondria-ER appositions are destroyed during mitophagy, and reducing mitochondria-ER contacts increases the rate of mitochondrial degradation. Mechanistically, parkin/PINK1 catalyze a ... [more]
Throughput
- Low Throughput
Additional Notes
- #LPPI
- likely protein-protein interaction
Curated By
- BioGRID