SQSTM1
Gene Ontology Biological Process
- apoptotic signaling pathway [TAS]
- autophagy [IMP, TAS]
- endosomal transport [TAS]
- intracellular signal transduction [TAS]
- macroautophagy [ISS]
- negative regulation of apoptotic process [TAS]
- neurotrophin TRK receptor signaling pathway [TAS]
- positive regulation of apoptotic process [TAS]
- positive regulation of macroautophagy [IMP]
- positive regulation of transcription from RNA polymerase II promoter [TAS]
- protein localization [TAS]
- protein phosphorylation [NAS]
- regulation of I-kappaB kinase/NF-kappaB signaling [IMP]
- regulation of Ras protein signal transduction [NAS]
- response to stress [TAS]
- ubiquitin-dependent protein catabolic process [TAS]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
PRKCI
Gene Ontology Biological Process
- Golgi vesicle budding [ISO]
- actin filament organization [IMP]
- cell migration [ISO]
- cell-cell junction organization [ISO]
- cellular protein localization [ISO]
- cellular response to insulin stimulus [IMP, ISO]
- establishment of apical/basal cell polarity [IMP]
- eye photoreceptor cell development [IMP]
- negative regulation of glial cell apoptotic process [ISO]
- negative regulation of neuron apoptotic process [ISO]
- positive regulation of NF-kappaB transcription factor activity [ISO]
- positive regulation of endothelial cell apoptotic process [ISO]
- positive regulation of establishment of protein localization to plasma membrane [IMP]
- positive regulation of glial cell proliferation [ISO]
- positive regulation of glucose import [IMP]
- positive regulation of neuron projection development [ISO]
- protein phosphorylation [IDA, ISO]
- response to interleukin-1 [ISO]
- response to peptide hormone [ISO]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
- Golgi membrane [ISO]
- Schmidt-Lanterman incisure [IDA]
- apical part of cell [IDA]
- apical plasma membrane [IDA]
- cell leading edge [ISO]
- cytoplasm [IDA, ISO]
- cytosol [ISO]
- extracellular vesicular exosome [ISO]
- intercellular bridge [ISO]
- microtubule cytoskeleton [ISO]
- nucleus [IDA, ISO]
- plasma membrane [ISO]
- protein complex [ISO]
- tight junction [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
Aurothiomalate inhibits transformed growth by targeting the PB1 domain of protein kinase Ciota.
We recently identified the gold compound aurothiomalate (ATM) as a potent inhibitor of the Phox and Bem1p (PB1)-PB1 domain interaction between protein kinase C (PKC) iota and the adaptor molecule Par6. ATM also blocks oncogenic PKCiota signaling and the transformed growth of human lung cancer cells. Here we demonstrate that ATM is a highly selective inhibitor of PB1-PB1 domain interactions ... [more]
Throughput
- Low Throughput
Additional Notes
- interaction inhibited in the presence of Aurothiomalate
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| PRKCI SQSTM1 | Affinity Capture-MS Affinity Capture-MS 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 is identified by mass spectrometric methods. | High | - | BioGRID | 1463676 |
Curated By
- BioGRID