CASK
Gene Ontology Biological Process
- cell adhesion [TAS]
- extracellular matrix organization [TAS]
- negative regulation of cell-matrix adhesion [IMP]
- negative regulation of cellular response to growth factor stimulus [IMP]
- negative regulation of keratinocyte proliferation [IMP]
- negative regulation of wound healing [IMP]
- nucleotide phosphorylation [TAS]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
RPH3A
Gene Ontology Molecular Function- calcium ion binding [ISS]
- calcium-dependent phospholipid binding [ISS]
- inositol 1,4,5 trisphosphate binding [ISS]
- phosphate ion binding [ISS]
- phosphatidylinositol phosphate binding [TAS]
- phosphatidylinositol-4,5-bisphosphate binding [ISS]
- protein binding [IPI]
- protein complex binding [ISS]
- selenium binding [ISS]
- zinc ion binding [ISS]
- calcium ion binding [ISS]
- calcium-dependent phospholipid binding [ISS]
- inositol 1,4,5 trisphosphate binding [ISS]
- phosphate ion binding [ISS]
- phosphatidylinositol phosphate binding [TAS]
- phosphatidylinositol-4,5-bisphosphate binding [ISS]
- protein binding [IPI]
- protein complex binding [ISS]
- selenium binding [ISS]
- zinc ion binding [ISS]
Gene Ontology Cellular Component
Reconstituted Complex
An interaction is detected between purified proteins in vitro.
Publication
The scaffolding protein CASK mediates the interaction between rabphilin3a and beta-neurexins.
CASK, a member of the membrane-associated guanylate kinase (MAGUK) superfamily, binds to the carboxyl-terminus of beta-neurexins on the intracellular side of the presynaptic membrane. The guanylate kinase-like (GUK) domains of MAGUKs lack kinase activities, but might be important for mediating specific protein-protein interaction. By a yeast two-hybrid approach, we identified an interaction between the GUK domain of CASK and the ... [more]
Throughput
- Low Throughput
Related interactions
Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
---|---|---|---|---|---|---|
CASK RPH3A | 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