ITGB3
Gene Ontology Biological Process
- activation of protein kinase activity [ISO]
- apolipoprotein A-I-mediated signaling pathway [ISO]
- cell adhesion [ISO]
- cell growth [ISO]
- cell migration [ISO]
- cell projection morphogenesis [IC]
- cell-matrix adhesion [IGI, ISO]
- cell-substrate adhesion [ISO]
- cell-substrate junction assembly [IDA]
- cellular calcium ion homeostasis [ISO]
- heterotypic cell-cell adhesion [ISO]
- integrin-mediated signaling pathway [ISO]
- negative chemotaxis [ISO]
- negative regulation of cell death [ISO]
- negative regulation of lipid storage [ISO]
- negative regulation of lipid transport [ISO]
- negative regulation of lipoprotein metabolic process [ISO]
- negative regulation of low-density lipoprotein particle receptor biosynthetic process [ISO]
- negative regulation of macrophage derived foam cell differentiation [ISO]
- platelet activation [ISO]
- platelet aggregation [ISO]
- positive regulation of ERK1 and ERK2 cascade [ISO]
- positive regulation of MAPK cascade [ISO]
- positive regulation of adenylate cyclase-inhibiting opioid receptor signaling pathway [ISO]
- positive regulation of angiogenesis [ISO]
- positive regulation of bone resorption [IC, ISO]
- positive regulation of cell adhesion mediated by integrin [ISO]
- positive regulation of cell migration [IMP]
- positive regulation of endothelial cell migration [ISO]
- positive regulation of endothelial cell proliferation [ISO]
- positive regulation of fibroblast migration [ISO]
- positive regulation of glomerular mesangial cell proliferation [ISO]
- positive regulation of leukocyte migration [ISO]
- positive regulation of osteoblast proliferation [IMP]
- positive regulation of osteoclast differentiation [IC]
- positive regulation of peptidyl-tyrosine phosphorylation [ISO]
- positive regulation of smooth muscle cell migration [ISO]
- positive regulation of smooth muscle cell proliferation [ISO]
- protein folding [ISO]
- regulation of G-protein coupled receptor protein signaling pathway [ISO]
- regulation of cell migration [IMP]
- regulation of release of sequestered calcium ion into cytosol [ISO]
- smooth muscle cell migration [ISO]
- substrate adhesion-dependent cell spreading [ISO]
- viral entry into host cell [ISO]
Gene Ontology Molecular Function- cell adhesion molecule binding [ISO]
- extracellular matrix binding [ISO]
- fibrinogen binding [ISO]
- fibronectin binding [ISO]
- identical protein binding [ISO]
- integrin binding [IPI]
- peptide binding [ISO]
- protease binding [ISO]
- protein binding [IPI]
- protein disulfide isomerase activity [ISO]
- vascular endothelial growth factor receptor 2 binding [ISO]
- cell adhesion molecule binding [ISO]
- extracellular matrix binding [ISO]
- fibrinogen binding [ISO]
- fibronectin binding [ISO]
- identical protein binding [ISO]
- integrin binding [IPI]
- peptide binding [ISO]
- protease binding [ISO]
- protein binding [IPI]
- protein disulfide isomerase activity [ISO]
- vascular endothelial growth factor receptor 2 binding [ISO]
Gene Ontology Cellular Component
- alpha9-beta1 integrin-ADAM8 complex [IDA]
- apical plasma membrane [IDA, ISO]
- cell surface [ISO]
- external side of plasma membrane [IDA]
- extracellular vesicular exosome [ISO]
- filopodium membrane [ISO]
- focal adhesion [ISO]
- integrin alpha9-beta1 complex [TAS]
- integrin alphav-beta3 complex [ISO]
- integrin complex [ISO]
- lamellipodium membrane [ISO]
- melanosome [ISO]
- membrane [ISO]
- microvillus membrane [ISO]
- nucleus [ISO]
- plasma membrane [ISO]
- receptor complex [ISO]
- ruffle membrane [ISO]
PRKDC
Gene Ontology Biological Process
- B cell lineage commitment [IMP]
- T cell differentiation in thymus [IMP]
- T cell lineage commitment [IMP]
- T cell receptor V(D)J recombination [IMP]
- V(D)J recombination [IGI]
- brain development [IGI]
- cellular response to insulin stimulus [ISO]
- double-strand break repair [IMP]
- double-strand break repair via homologous recombination [IBA]
- double-strand break repair via nonhomologous end joining [IMP]
- ectopic germ cell programmed cell death [IMP]
- heart development [IGI]
- immunoglobulin V(D)J recombination [IMP]
- immunoglobulin production [ISO]
- intrinsic apoptotic signaling pathway in response to DNA damage [IMP]
- lymphocyte differentiation [IMP]
- negative regulation of cellular senescence [ISO]
- negative regulation of protein phosphorylation [IMP]
- negative regulation of response to gamma radiation [ISO]
- peptidyl-serine phosphorylation [ISO]
- phosphorylation [IBA]
- positive regulation of apoptotic process [IMP]
- positive regulation of developmental growth [ISO]
- positive regulation of fibroblast proliferation [ISO]
- positive regulation of immune system process [ISO]
- positive regulation of transcription from RNA polymerase II promoter [ISO]
- pro-B cell differentiation [IMP]
- protein destabilization [IDA]
- protein phosphorylation [IDA]
- regulation of circadian rhythm [IMP]
- response to gamma radiation [IMP]
- signal transduction involved in mitotic G1 DNA damage checkpoint [ISO]
- somitogenesis [IGI]
- spleen development [ISO]
- telomere maintenance [IMP]
- thymus development [ISO]
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
LCP1 preferentially binds clasped ?M?2 integrin and attenuates leukocyte adhesion under flow.
Integrins are ?/? heterodimers that interconvert between inactive and active states. In the active state the ?/? cytoplasmic domains recruit integrin-activating proteins and separate the transmembrane and cytoplasmic (TMcyto) domains (unclasped TMcyto). Conversely, in the inactive state the ?/? TMcyto domains bind integrin-inactivating proteins, resulting in the association of the TMcyto domains (clasped TMcyto). Here, we report the isolation of ... [more]
Throughput
- High Throughput
Curated By
- BioGRID