PKD1
Gene Ontology Biological Process
- JAK-STAT cascade [ISS]
- anatomical structure morphogenesis [TAS]
- branching morphogenesis of an epithelial tube [IDA]
- calcium ion transmembrane transport [ISS]
- calcium-independent cell-matrix adhesion [TAS]
- cartilage development [IEP]
- cell cycle arrest [ISS]
- cell-matrix adhesion [TAS]
- cytoplasmic sequestering of transcription factor [ISS]
- detection of mechanical stimulus [IBA, ISS]
- digestive tract development [IEP]
- embryonic placenta development [ISS]
- genitalia development [IEP]
- heart development [IEP]
- homophilic cell adhesion via plasma membrane adhesion molecules [TAS]
- in utero embryonic development [ISS]
- kidney development [ISS]
- lung epithelium development [IEP]
- mesonephric duct development [IEP]
- mesonephric tubule development [IEP]
- metanephric ascending thin limb development [IEP]
- metanephric collecting duct development [IEP]
- metanephric distal tubule morphogenesis [IEP]
- metanephric proximal tubule development [IEP]
- neural tube development [IEP]
- peptidyl-serine phosphorylation [ISS]
- placenta blood vessel development [ISS]
- positive regulation of cyclin-dependent protein serine/threonine kinase activity involved in G1/S transition of mitotic cell cycle [IDA]
- positive regulation of protein binding [ISS]
- positive regulation of transcription from RNA polymerase II promoter [IDA]
- protein export from nucleus [ISS]
- regulation of proteasomal protein catabolic process [IDA]
- skin development [IEP]
- spinal cord development [IEP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
RGS7
Gene Ontology Biological Process
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
Interaction between RGS7 and polycystin.
Regulators of G protein signaling (RGS) proteins accelerate the intrinsic GTPase activity of certain Galpha subunits and thereby modulate a number of G protein-dependent signaling cascades. Currently, little is known about the regulation of RGS proteins themselves. We identified a short-lived RGS protein, RGS7, that is rapidly degraded through the proteasome pathway. The degradation of RGS7 is inhibited by interaction ... [more]
Throughput
- Low Throughput
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| PKD1 RGS7 | Reconstituted Complex Reconstituted Complex An interaction is detected between purified proteins in vitro. | Low | - | BioGRID | - | |
| PKD1 RGS7 | Two-hybrid Two-hybrid Bait protein expressed as a DNA binding domain (DBD) fusion and prey expressed as a transcriptional activation domain (TAD) fusion and interaction measured by reporter gene activation. | Low | - | BioGRID | - |
Curated By
- BioGRID