SCUBA

SH3BP1 — SH3 domain binding protein 1

SH3BP1 belongs to a gene co-expression module in 4 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

SH3BP1's module in each cell type

Cell typeModuleShares the module with
CD4⁺ T cellsTh17 lineage
Th17 fate
ADA, ARHGEF3, CD226, CD52, DENND3, EVL, IDH2, IL17RE +13 moreView in SCUBA
Innate lymphoid cellsActin Cytoskeleton Dynamics
Cytoskeleton & motility
ACTN4, ALDH9A1, APBB1IP, ARHGAP10, CDC37, CXXC5, FAM136A, FERMT3 +26 moreView in SCUBA
Mucosal-associated invariant T cellCytoskeletal Remodeling Migration
migration & adhesion
ADAM8, BIN2, C11orf21, CAPN1, CAPN2, CD52, CDC25B, CNN2 +14 more
Natural Killer cellsResident NK cells
Gut residency
ANXA11, APBB1IP, CD151, CXXC5, HMOX2, LSP1, MPG, PPDPF +4 moreView in SCUBA

About the gene

SynonymsARHGAP43
Chromosome22: 37634654-37656117
Predicted locationIntracellular
Essential geneNo
Protein classMetabolic proteins, Predicted intracellular proteins
Molecular functionGTPase activation
Biological processPhagocytosis

Function

GTPase activating protein (GAP) which specifically converts GTP-bound Rho-type GTPases including RAC1 and CDC42 in their inactive GDP-bound form. By specifically inactivating RAC1 at the leading edge of migrating cells, it regulates the spatiotemporal organization of cell protrusions which is important for proper cell migration. Also negatively regulates CDC42 in the process of actin remodeling and the formation of epithelial cell junctions. Through its GAP activity toward RAC1 and/or CDC42 plays a specific role in phagocytosis of large particles. Specifically recruited by a PI3 kinase/PI3K-dependent mechanism to sites of large particles engagement, inactivates RAC1 and/or CDC42 allowing the reorganization of the underlying actin cytoskeleton required for engulfment. It also plays a role in angiogenesis and the process of repulsive guidance as part of a semaphorin-plexin signaling pathway. Following the binding of PLXND1 to extracellular SEMA3E it dissociates from PLXND1 and inactivates RAC1, inducing the intracellular reorganization of the actin cytoskeleton and the collapse of cells.

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.