S100A7
Gene Ontology Biological Process
- angiogenesis [NAS]
- defense response to Gram-negative bacterium [IMP]
- epidermis development [TAS]
- innate immune response [NAS]
- keratinocyte differentiation [NAS]
- positive regulation of ERK1 and ERK2 cascade [IDA]
- positive regulation of T cell chemotaxis [IDA]
- positive regulation of granulocyte chemotaxis [IDA]
- positive regulation of monocyte chemotaxis [IDA]
- response to lipopolysaccharide [IEP]
- response to reactive oxygen species [IDA]
- sequestering of metal ion [IDA]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
FABP5
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
Probable interaction between S100A7 and E-FABP in the cytosol of human keratinocytes from psoriatic scales.
The overexpression of E-FABP and S100A7 in lesional psoriatic skin suggests a possible link with this hyperproliferative skin disease. In order to investigate a role for the proteins in this disease, the purifications for both proteins were re-analyzed. Moreover, a specific antiserum directed against purified human S100A7 was generated. By SDS-PAGE immunoblotting we show that E-FABP and S100A7 are expressed ... [more]
Throughput
- Low Throughput
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| S100A7 FABP5 | 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 | - |
Curated By
- BioGRID