F2R
Gene Ontology Biological Process
- G-protein coupled receptor signaling pathway [ISS]
- STAT protein import into nucleus [IDA]
- activation of MAPKK activity [ISS]
- activation of cysteine-type endopeptidase activity involved in apoptotic process [IDA]
- anatomical structure morphogenesis [TAS]
- blood coagulation [TAS]
- connective tissue replacement involved in inflammatory response wound healing [IDA]
- establishment of synaptic specificity at neuromuscular junction [ISS]
- homeostasis of number of cells within a tissue [ISS]
- inflammatory response [ISS]
- negative regulation of cell proliferation [IDA]
- negative regulation of glomerular filtration [ISS]
- negative regulation of neuron apoptotic process [ISS]
- negative regulation of renin secretion into blood stream [ISS]
- phospholipase C-activating G-protein coupled receptor signaling pathway [IDA]
- platelet activation [IDA, TAS]
- platelet dense granule organization [IC]
- positive regulation of ERK1 and ERK2 cascade [ISS]
- positive regulation of I-kappaB kinase/NF-kappaB signaling [IEP]
- positive regulation of JAK-STAT cascade [IDA]
- positive regulation of MAPK cascade [IDA]
- positive regulation of Rho protein signal transduction [ISS]
- positive regulation of blood coagulation [IDA]
- positive regulation of calcium ion transport [ISS]
- positive regulation of cell migration [IMP]
- positive regulation of cell proliferation [ISS]
- positive regulation of collagen biosynthetic process [IDA]
- positive regulation of cysteine-type endopeptidase activity involved in apoptotic process [IDA]
- positive regulation of cytosolic calcium ion concentration [ISS]
- positive regulation of cytosolic calcium ion concentration involved in phospholipase C-activating G-protein coupled signaling pathway [ISS]
- positive regulation of interleukin-6 secretion [IDA]
- positive regulation of interleukin-8 secretion [IDA]
- positive regulation of phosphatidylinositol 3-kinase signaling [ISS]
- positive regulation of release of sequestered calcium ion into cytosol [IDA]
- positive regulation of smooth muscle contraction [ISS]
- positive regulation of transcription, DNA-templated [IDA]
- positive regulation of vasoconstriction [ISS]
- protein kinase C-activating G-protein coupled receptor signaling pathway [ISS]
- regulation of blood coagulation [IDA]
- regulation of interleukin-1 beta production [ISS]
- regulation of sensory perception of pain [ISS]
- release of sequestered calcium ion into cytosol [ISS]
- response to lipopolysaccharide [ISS]
- response to wounding [IDA]
- tyrosine phosphorylation of STAT protein [IDA]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
PDCD6IP
Gene Ontology Biological Process
- positive regulation of exosomal secretion [IMP]
- positive regulation of extracellular vesicular exosome assembly [IMP]
- regulation of extracellular vesicular exosome assembly [IMP]
- ubiquitin-independent protein catabolic process via the multivesicular body sorting pathway [IMP]
- viral budding via host ESCRT complex [IGI]
- viral life cycle [TAS]
- viral process [TAS]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
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 α-arrestin ARRDC3 mediates ALIX ubiquitination and G protein-coupled receptor lysosomal sorting.
The sorting of G protein-coupled receptors (GPCRs) to lysosomes is critical for proper signaling and cellular responses. We previously showed that the adaptor protein ALIX regulates lysosomal degradation of protease-activated receptor-1 (PAR1), a GPCR for thrombin, independent of ubiquitin-binding ESCRTs and receptor ubiquitination. However, the mechanisms that regulate ALIX function during PAR1 lysosomal sorting are not known. Here we show ... [more]
Throughput
- Low Throughput
Additional Notes
- Figure 5
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| F2R PDCD6IP | 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 | - | |
| F2R PDCD6IP | 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 | - | |
| PDCD6IP F2R | 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