MEP1A
Gene Ontology Cellular Component
CANX
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
- ER-mitochondrion membrane contact site [ISO]
- axon [ISO]
- cell [IMP]
- cytoplasm [ISO]
- dendrite cytoplasm [ISO]
- dendritic spine [ISO]
- endoplasmic reticulum [IDA, ISO]
- endoplasmic reticulum membrane [ISO]
- integral component of membrane [IDA]
- membrane [IDA, ISO]
- myelin sheath [IDA]
- neuronal cell body [ISO]
- protein complex [ISO]
- ribosome [ISO]
- rough endoplasmic reticulum [ISO]
- smooth endoplasmic reticulum [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
Chaperone interactions of the metalloproteinase meprin A in the secretory or proteasomal-degradative pathway.
The secreted form of mouse meprin A is a homooligomer of meprin alpha subunits that contain a prosequence, a catalytic domain, and three domains designated as MAM (meprin, A5 protein, receptor protein-tyrosine phosphatase mu), MATH (meprin and TRAF homology), and AM (AfterMath). Previous studies indicated that wild-type mouse meprin alpha is predominantly a secreted protein, while the MAM deletion mutant ... [more]
Throughput
- Low Throughput
Curated By
- BioGRID