RAPSN
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
DAG1
Gene Ontology Biological Process
- NLS-bearing protein import into nucleus [ISO]
- Schwann cell development [IMP]
- basement membrane organization [IMP]
- branching involved in salivary gland morphogenesis [IMP]
- calcium-dependent cell-matrix adhesion [ISO]
- commissural neuron axon guidance [IMP]
- cytoskeletal anchoring at plasma membrane [ISO]
- epithelial tube branching involved in lung morphogenesis [IMP]
- membrane protein ectodomain proteolysis [ISO]
- microtubule anchoring [ISO]
- modulation by virus of host morphology or physiology [ISO]
- morphogenesis of an epithelial sheet [IMP]
- myelination in peripheral nervous system [IMP]
- negative regulation of MAPK cascade [ISO]
- negative regulation of cell migration [ISO]
- negative regulation of protein kinase B signaling [ISO]
- nerve maturation [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
- basement membrane [IDA, ISO]
- basolateral plasma membrane [ISO]
- cell outer membrane [IDA]
- cell-cell adherens junction [ISO]
- cell-cell junction [IDA]
- contractile ring [ISO]
- costamere [ISO]
- cytoplasm [ISO]
- dystroglycan complex [IDA]
- dystrophin-associated glycoprotein complex [ISO]
- extracellular space [ISO]
- extracellular vesicular exosome [ISO]
- filopodium [ISO]
- focal adhesion [ISO]
- integral component of membrane [ISO]
- lamellipodium [ISO]
- membrane [IDA]
- membrane raft [IDA]
- node of Ranvier [IMP]
- nucleoplasm [ISO]
- plasma membrane [IDA, ISO]
- sarcolemma [IDA, ISO]
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
Autoantibody of NRIP, a novel AChR-interacting protein, plays a detrimental role in myasthenia gravis.
Nuclear receptor interaction protein (NRIP) co-localizes with acetylcholine receptor (AChR) at the neuromuscular junction (NMJ), and NRIP deficiency causes aberrant NMJ architecture. However, the normal physiological and pathophysiological roles of NRIP in NMJ are still unclear.We investigated the co-localization and interaction of NRIP with AChR-associated proteins using immunofluorescence and immunoprecipitation assay, respectively. The binding affinity of AChR-associated proteins was analysed ... [more]
Throughput
- Low Throughput
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| RAPSN DAG1 | Co-fractionation Co-fractionation Interaction inferred from the presence of two or more protein subunits in a partially purified protein preparation. If co-fractionation is demonstrated between 3 or more proteins, then add them as a complex. | High | 0.996 | BioGRID | 2679442 |
Curated By
- BioGRID