SLC2A1
Gene Ontology Biological Process
Gene Ontology Molecular Function- D-glucose transmembrane transporter activity [IDA, ISO]
- dehydroascorbic acid transporter activity [IDA, ISO]
- glucose transmembrane transporter activity [IDA, ISO]
- identical protein binding [ISO]
- kinase binding [IPI]
- protein binding [IPI]
- protein self-association [ISO, ISS]
- sugar:proton symporter activity [TAS]
- xenobiotic transporter activity [IDA]
- D-glucose transmembrane transporter activity [IDA, ISO]
- dehydroascorbic acid transporter activity [IDA, ISO]
- glucose transmembrane transporter activity [IDA, ISO]
- identical protein binding [ISO]
- kinase binding [IPI]
- protein binding [IPI]
- protein self-association [ISO, ISS]
- sugar:proton symporter activity [TAS]
- xenobiotic transporter activity [IDA]
Gene Ontology Cellular Component
- basolateral plasma membrane [ISO]
- blood microparticle [ISO]
- caveola [IDA]
- cell-cell junction [IDA]
- cortical actin cytoskeleton [ISO, ISS]
- cytoplasm [IDA, ISO]
- cytosol [ISO]
- extracellular vesicular exosome [ISO]
- female pronucleus [ISO]
- integral component of membrane [TAS]
- integral component of plasma membrane [ISO, ISS]
- intracellular [ISO]
- membrane [ISO]
- membrane raft [ISO]
- midbody [ISO]
- plasma membrane [IDA, ISO]
- vesicle [ISO]
UBC
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
Downregulation of retinal GLUT1 in diabetes by ubiquitinylation.
To investigate the effect of chronic hyperglycemia on the levels of the glucose transporter GLUT1 in retina and its ubiquitinylation.Two diabetic animal models (Goto Kakizaki rats and alloxan-induced diabetic rabbits) and retinal endothelial cells in culture were used. GLUT1 content was determined by western blotting. Glut1 mRNA was determined by RT-PCR and northern blotting. Ubiquitin conjugates were evaluated by western ... [more]
Throughput
- Low Throughput
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| UBC SLC2A1 | Affinity Capture-MS Affinity Capture-MS 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 is identified by mass spectrometric methods. | Low | - | BioGRID | - |
Curated By
- BioGRID