ICAM1
Gene Ontology Biological Process
- T cell activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell [IMP]
- adhesion of symbiont to host [IDA]
- cell adhesion [IDA]
- cytokine-mediated signaling pathway [TAS]
- establishment of endothelial barrier [IGI]
- extracellular matrix organization [TAS]
- heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules [TAS]
- interferon-gamma-mediated signaling pathway [TAS]
- leukocyte cell-cell adhesion [IMP]
- leukocyte migration [IEP]
- membrane to membrane docking [IEP]
- negative regulation of endothelial cell apoptotic process [IDA]
- negative regulation of extrinsic apoptotic signaling pathway via death domain receptors [IDA]
- positive regulation of ERK1 and ERK2 cascade [IMP]
- positive regulation of cellular extravasation [IMP]
- receptor-mediated virion attachment to host cell [IDA]
- regulation of immune response [TAS]
- regulation of leukocyte mediated cytotoxicity [TAS]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
ITGAL
Gene Ontology Biological Process
- T cell activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell [IMP]
- blood coagulation [TAS]
- cell adhesion [NAS]
- cell-matrix adhesion [IMP]
- cellular component movement [TAS]
- extracellular matrix organization [TAS]
- heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules [IMP]
- inflammatory response [NAS]
- leukocyte cell-cell adhesion [IMP]
- leukocyte migration [TAS]
- receptor clustering [IMP]
- regulation of immune response [TAS]
- signal transduction [NAS]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Reconstituted Complex
An interaction is inferred between proteins in vitro. This can include proteins in recombinant form or proteins isolated directly from cells with recombinant or purified bait. For example, GST pull-down assays where a GST-tagged protein is first isolated and then used to fish interactors from cell lysates are considered reconstituted complexes (e.g. PUBMED: 14657240, Fig. 4A or PUBMED: 14761940, Fig. 5). This can also include gel-shifts, surface plasmon resonance, isothermal titration calorimetry (ITC) and bio-layer interferometry (BLI) experiments. The bait-hit directionality may not be clear for 2 interacting proteins. In these cases the directionality is up to the discretion of the curator.
Publication
Association of the membrane proximal regions of the alpha and beta subunit cytoplasmic domains constrains an integrin in the inactive state.
The adhesiveness of integrins is regulated through a process termed "inside-out" signaling. To understand the molecular mechanism of integrin inside-out signaling, we generated K562 stable cell lines that expressed LFA-1 (alpha(L)beta(2)) or Mac-1 (alpha(M)beta(2)) with mutations in the cytoplasmic domain. Complete truncation of the beta(2) cytoplasmic domain, but not a truncation that retained the membrane proximal eight residues, resulted in ... [more]
Throughput
- Low Throughput
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| ITGAL ICAM1 | Co-crystal Structure Co-crystal Structure Interaction directly demonstrated at the atomic level by X-ray crystallography. Also used for NMR or Electron Microscopy (EM) structures. If there is no obvious bait-hit directionality to the interaction involving 3 or more proteins, then the co-crystallized proteins should be listed as a complex. | Low | - | BioGRID | - | |
| ICAM1 ITGAL | FRET FRET An interaction is inferred when close proximity of interaction partners is detected by fluorescence resonance energy transfer between pairs of fluorophore-labeled molecules, such as occurs between CFP (donor) and YFP (acceptor) fusion proteins. | Low | - | BioGRID | 2598591 | |
| ICAM1 ITGAL | Reconstituted Complex Reconstituted Complex An interaction is inferred between proteins in vitro. This can include proteins in recombinant form or proteins isolated directly from cells with recombinant or purified bait. For example, GST pull-down assays where a GST-tagged protein is first isolated and then used to fish interactors from cell lysates are considered reconstituted complexes (e.g. PUBMED: 14657240, Fig. 4A or PUBMED: 14761940, Fig. 5). This can also include gel-shifts, surface plasmon resonance, isothermal titration calorimetry (ITC) and bio-layer interferometry (BLI) experiments. The bait-hit directionality may not be clear for 2 interacting proteins. In these cases the directionality is up to the discretion of the curator. | Low | - | BioGRID | - |
Curated By
- BioGRID