SELPLG

P-selectin UniProt accession P16109

Ca(2+)-dependent receptor for myeloid cells that binds to carbohydrates on neutrophils and monocytes. Mediates the interaction of activated endothelial cells or platelets with leukocytes. The ligand recognized is sialyl-Lewis X.

Mediates rapid rolling of leukocyte rolling over vascular surfaces during the initial steps in inflammation through interaction with SELPLG. Mediates cell-cell interactions and cell adhesion via the interaction with integrin alpha-IIb/beta3 (ITGA2B:ITGB3) and integrin alpha-V/beta-3 (ITGAV:ITGB3) (PubMed:37184585)

Source: UniProt

Interacts with SNX17. Interacts with SELPLG/PSGL1 and PODXL2 and mediates neutrophil adhesion and leukocyte rolling. This interaction requires the sialyl-Lewis X epitope of SELPLG and PODXL2, and specific tyrosine sulfation on SELPLG.

Interacts (via C-type lectin domain) with alpha-IIb/beta3 integrin ITGA2B:ITGB3 and alpha-V/beta-3 integrin ITGAV:ITGB3 (PubMed:37184585). Interacts with alpha5/beta1 integrin ITGA5:ITGB1 and alpha4/beta1 integrin ITGA4:ITGB (PubMed:37184585)

Source: UniProt
Cell membrane — Single-pass type I membrane protein
Source: UniProt

Stored in the alpha-granules of platelets and Weibel-Palade bodies of endothelial cells. Upon cell activation by agonists, P-selectin is transported rapidly to the cell surface

Source: UniProt

The C-type lectin domain is required for binding to integrins (PubMed:37184585). Binding to soluble integrins alpha-V/beta-3 (ITGAV:ITGB3) and alpha-IIb/beta3 (ITGA2B:ITGB) is cation-dependent in order of preference of 1 mM Mn(2+) > Mg(2+) > Ca(2+) (PubMed:37184585). Binds to the allosteric site (site 2) of integrins and activates them (PubMed:37184585).

The interaction with integrins may mediate cell-cell interactions and cell adhesion (PubMed:37184585)

Source: UniProt

Click a pathway to open the interactive Reactome viewer.

Pathway list and interactive viewer: Reactome

Synthetic Lethal Network

Genes with an experimentally identified or computationally predicted synthetic-lethal relationship to SELPLG, aggregated across our SSL data sources. Click any partner node to view that gene’s page.

Nodes and edges are coloured by the SSL data source. Partners appearing in more than one source are shown in grey.

BioGRID SLOrth SynLethDB MexDrugs Multi-source
Sources: BioGRID, SLOrth, SynLethDB, MexDrugs

Clinical Trials

Total Trials Found: 30

NCT ID Condition Brief Title Phase Status
NCT03938454 Priapism A Study to Evaluate the Safety and Efficacy of Crizanlizumab in Sickle Cell Disease Related Priapism PHASE2 COMPLETED
NCT01895725 Cardiovascular Risk Factors, Coronary Artery Disease, Cerebrovascular Disease, Peripheral Artery Disease Correlation of Artherosclerotic Plaque Volume and Intima Media Thickness With Soluble P-selectin N/A ACTIVE_NOT_RECRUITING
NCT05864079 Overweight and Obesity Developmental Endothelial Locus-1, Platelet Count, and Soluble P-selectin in Overweight and Obese Subjects N/A COMPLETED
NCT03812328 Venous Thromboembolism Study to Assess the Safety and Efficacy of SelK2 to Prevent Blood Clots in Patients Undergoing Total Knee Replacement PHASE2 COMPLETED
NCT04505774 Covid19 Accelerating COVID-19 Therapeutic Interventions and Vaccines 4 ACUTE PHASE4 COMPLETED
NCT04540042 Asthma, Chronic Obstructive Pulmonary Disease Study to Assess the Safety and Efficacy of SelK2 on Airway Responses Following Allergen Challenge in Subjects With Asthma (Part 1) and in Subjects With Chronic Obstructive Pulmonary Disease (Part 2) PHASE2 COMPLETED
NCT03474965 Sickle Cell Disease (SCD) Study of Dose Confirmation and Safety of Crizanlizumab in Pediatric Sickle Cell Disease Patients PHASE2 COMPLETED
NCT02896543 Acute Myocardial Infarction The Relationship of Change of Dendritic Cells Fractalkine and P-selectin Patients With Acute Myocardial Infarction N/A COMPLETED
NCT02649660 Fabry Disease Lipidomics and Functional Analyses of Platelets in Fabry Disease N/A UNKNOWN
NCT04662931 Sickle Cell Disease (SCD) An Indian Multi-centric Phase IV Study to Assess the Safety of Crizanlizumab in Sickle Cell Disease Patients PHASE4 COMPLETED