HSPA4
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
MME
Gene Ontology Biological Process
- angiotensin maturation [TAS]
- beta-amyloid metabolic process [ISS]
- cellular protein metabolic process [TAS]
- cellular response to UV-A [IDA]
- cellular response to UV-B [IDA]
- cellular response to cytokine stimulus [IDA]
- creatinine metabolic process [IMP]
- kidney development [IEP]
- peptide metabolic process [ISS]
- proteolysis [IDA]
- replicative senescence [IEP]
- sensory perception of pain [ISS]
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
HSP27 and HSP70 interact with CD10 in C4-2 prostate cancer cells.
CD10 is an approximately 100 kDa transmembrane metallo-endopeptidase. CD10 is strongly expressed by normal prostate epithelium. While only 30% of primary prostate tumors express CD10, it is strongly expressed by most lymph node metastases. The function of CD10 and the interaction between CD10 and other cellular proteins in prostate cancer (CaP) is not well defined. Cellular context may ultimately determine ... [more]
Throughput
- Low Throughput
Ontology Terms
- lncap-c42b4 cell (BTO:0002998)
- prostate cancer (DOID:10283)
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| MME HSPA4 | 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 | 568807 |
Curated By
- BioGRID