PLEKHG5
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
GIPC1
Gene Ontology Biological Process
- G-protein coupled receptor signaling pathway [TAS]
- endothelial cell migration [IMP]
- glutamate secretion [IMP]
- negative regulation of proteasomal ubiquitin-dependent protein catabolic process [IDA]
- positive regulation of GTPase activity [TAS]
- positive regulation of cytokinesis [ISO]
- positive regulation of transforming growth factor beta receptor signaling pathway [IDA]
- protein targeting [IMP, IPI]
- regulation of protein stability [IDA]
- regulation of synaptic plasticity [IMP]
- synaptic transmission [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
- brush border [ISO]
- cell [IMP]
- cell cortex [ISO]
- cytoplasm [IDA]
- cytoplasmic membrane-bounded vesicle [ISO]
- cytosol [IDA, ISO]
- dendritic shaft [IDA]
- dendritic spine [IDA]
- endocytic vesicle [ISO]
- extracellular vesicular exosome [ISO]
- intracellular [IMP]
- membrane [IDA, ISO]
- synaptic vesicle [IDA]
- vesicle membrane [IDA]
Protein-peptide
An interaction is detected between a protein and a peptide derived from an interaction partner. This includes phage display experiments.
Publication
The Amot/Patj/Syx signaling complex spatially controls RhoA GTPase activity in migrating endothelial cells.
Controlled regulation of Rho GTPase activity is an essential component mediating growth factor-stimulated migration. We have previously shown that angiomotin (Amot), a membrane-associated scaffold protein, plays a critical role during vascular patterning and endothelial migration during embryogenesis. However, the signaling pathways by which Amot controls directional migration are not known. Here we have used peptide pull-down and yeast 2-hybrid (Y2H) ... [more]
Throughput
- Low Throughput
Additional Notes
- Syx peptides were used in the experiment.
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| GIPC1 PLEKHG5 | 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 | - | |
| PLEKHG5 GIPC1 | 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 | - |
Curated By
- BioGRID