BAG2
Gene Ontology Biological Process
Gene Ontology Molecular Function
PINK1
Gene Ontology Biological Process
- TORC2 signaling [IC]
- activation of protein kinase B activity [IC]
- cellular response to hypoxia [IMP]
- cellular response to toxic substance [TAS]
- intracellular signal transduction [IDA]
- mitochondrion degradation [IMP]
- mitochondrion organization [IMP]
- negative regulation of JNK cascade [TAS]
- negative regulation of gene expression [ISS]
- negative regulation of hydrogen peroxide-induced neuron intrinsic apoptotic signaling pathway [IDA, IMP]
- negative regulation of neuron apoptotic process [IMP]
- negative regulation of oxidative stress-induced cell death [IDA]
- negative regulation of oxidative stress-induced intrinsic apoptotic signaling pathway [IDA]
- negative regulation of oxidative stress-induced neuron death [TAS]
- negative regulation of reactive oxygen species metabolic process [IMP]
- peptidyl-serine autophosphorylation [TAS]
- peptidyl-serine phosphorylation [IDA, TAS]
- phosphorylation [NAS]
- positive regulation of I-kappaB kinase/NF-kappaB signaling [IDA]
- positive regulation of mitochondrial electron transport, NADH to ubiquinone [TAS]
- positive regulation of mitochondrial fission [IBA]
- positive regulation of peptidase activity [TAS]
- positive regulation of peptidyl-serine phosphorylation [IDA, TAS]
- positive regulation of protein kinase B signaling [IC]
- positive regulation of release of cytochrome c from mitochondria [IMP]
- positive regulation of ubiquitin-protein transferase activity [TAS]
- protein phosphorylation [IDA, TAS]
- protein ubiquitination [IMP]
- regulation of mitochondrial membrane potential [IGI, IMP]
- regulation of mitochondrion degradation [TAS]
- regulation of protein complex assembly [IDA]
- regulation of protein ubiquitination [IDA]
- regulation of reactive oxygen species metabolic process [IGI, IMP]
- regulation of synaptic vesicle transport [TAS]
- response to oxidative stress [IGI]
- response to stress [IDA]
- ubiquitin-dependent protein catabolic process [TAS]
Gene Ontology Molecular Function- ATP binding [IDA]
- C3HC4-type RING finger domain binding [IPI]
- calcium-dependent protein kinase activity [IDA]
- kinase activity [IDA, NAS]
- magnesium ion binding [IDA]
- peptidase activator activity [TAS]
- protease binding [IPI, TAS]
- protein binding [IPI]
- protein kinase B binding [IDA]
- protein serine/threonine kinase activity [IDA, TAS]
- ubiquitin protein ligase binding [IPI]
- ATP binding [IDA]
- C3HC4-type RING finger domain binding [IPI]
- calcium-dependent protein kinase activity [IDA]
- kinase activity [IDA, NAS]
- magnesium ion binding [IDA]
- peptidase activator activity [TAS]
- protease binding [IPI, TAS]
- protein binding [IPI]
- protein kinase B binding [IDA]
- protein serine/threonine kinase activity [IDA, TAS]
- ubiquitin protein ligase binding [IPI]
Gene Ontology Cellular Component
- Lewy body [TAS]
- TORC2 complex [IPI]
- astrocyte projection [IDA]
- axon [IDA]
- cell body [IDA]
- chromatin [IDA]
- cytoplasm [IDA]
- cytoskeleton [IDA]
- cytosol [IDA]
- integral component of mitochondrial outer membrane [IDA]
- membrane [IDA]
- mitochondrial inner membrane [IDA]
- mitochondrial intermembrane space [IDA]
- mitochondrial outer membrane [IDA]
- mitochondrion [IDA]
- nucleus [IDA]
- perinuclear region of cytoplasm [IDA]
Affinity Capture-Western
An interaction is inferred when a bait protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and the associated interaction partner identified by Western blot with a specific polyclonal antibody or second epitope tag. This category is also used if an interacting protein is visualized directly by dye stain or radioactivity. Note that this differs from any co-purification experiment involving affinity capture in that the co-purification experiment involves at least one extra purification step to get rid of potential contaminating proteins.
Publication
The BAG2 protein stabilises PINK1 by decreasing its ubiquitination.
Mutations in the PTEN-induced putative kinase 1 (PINK1) gene cause an autosomal recessive form of Parkinson disease (PD). Thus far, little is known about what can regulate the ubiquitin proteasome pathway of PINK1. Here, we report BAG2 (Bcl-2-associated athanogene family protein 2), a member of the BAG family, which directly binds with and stabilises PINK1 by decreasing its ubiquitination. Moreover, ... [more]
Throughput
- Low Throughput
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| PINK1 BAG2 | Affinity Capture-Western Affinity Capture-Western An interaction is inferred when a bait protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and the associated interaction partner identified by Western blot with a specific polyclonal antibody or second epitope tag. This category is also used if an interacting protein is visualized directly by dye stain or radioactivity. Note that this differs from any co-purification experiment involving affinity capture in that the co-purification experiment involves at least one extra purification step to get rid of potential contaminating proteins. | Low | - | BioGRID | - | |
| BAG2 PINK1 | Reconstituted Complex 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. | Low | - | BioGRID | - | |
| BAG2 PINK1 | Reconstituted Complex 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. | Low | - | BioGRID | - |
Curated By
- BioGRID