CAV2
Gene Ontology Biological Process
- caveola assembly [IMP]
- endoplasmic reticulum organization [ISS]
- mitochondrion organization [ISS]
- negative regulation of endothelial cell proliferation [ISS]
- positive regulation of dopamine receptor signaling pathway [IMP]
- regulation of mitosis [IEP]
- skeletal muscle fiber development [ISS]
- vesicle docking [IDA]
- vesicle fusion [IDA]
- vesicle organization [IDA]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
- Golgi apparatus [ISS]
- caveola [IDA]
- cytoplasmic vesicle [IDA]
- extrinsic component of cytoplasmic side of plasma membrane [IDA]
- integral component of plasma membrane [IDA]
- intracellular [IDA]
- membrane [IDA]
- membrane raft [IDA]
- perinuclear region of cytoplasm [IDA]
- plasma membrane [IDA]
- protein complex [IDA]
- transport vesicle [IDA]
KCNMA1
Gene Ontology Biological Process
- blood coagulation [TAS]
- cellular potassium ion homeostasis [IDA]
- micturition [IDA]
- negative regulation of cell volume [IDA]
- positive regulation of apoptotic process [IMP]
- potassium ion transmembrane transport [IBA, IDA]
- potassium ion transport [IDA]
- regulation of membrane potential [IDA]
- response to calcium ion [IDA]
- response to carbon monoxide [IDA, IMP]
- response to hypoxia [IDA]
- response to osmotic stress [IDA]
- smooth muscle contraction involved in micturition [IDA]
- synaptic transmission [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
Maxi-K channels localize to caveolae in human myometrium: a role for an actin-channel-caveolin complex in the regulation of myometrial smooth muscle K+ current.
Multiple cell-signaling pathways converge to modulate large-conductance, voltage- and Ca2+-sensitive K+ channel (maxi-K channel) activity and buffer cell excitability in human myometrial smooth muscle cells (hMSMCs). Recent evidence indicates that maxi-K channel proteins can target to membrane microdomains; however, their association with other proteins within these macromolecular complexes has not been elucidated. Biochemical isolation of detergent-resistant membrane fractions from human ... [more]
Throughput
- Low Throughput
Ontology Terms
- tissue: myometrium (BTO:0000907)
Additional Notes
- interaction detected in myometrium at non-pregnant and late pregnant
Related interactions
Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
---|---|---|---|---|---|---|
KCNMA1 CAV2 | 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 | 870130 |
Curated By
- BioGRID