Homo sapiens Protein: SEMA4D
Summary
InnateDB Protein IDBP-374808.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SEMA4D
Protein Name sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D
Synonyms C9orf164; CD100; coll-4; M-sema-G; SEMAJ;
Species Homo sapiens
Ensembl Protein ENSP00000391733
InnateDB Gene IDBG-75424 (SEMA4D)
Protein Structure
UniProt Annotation
Function Cell surface receptor for PLXN1B and PLXNB2 that plays an important role in cell-cell signaling. Promotes reorganization of the actin cytoskeleton and plays a role in axonal growth cone guidance in the developing central nervous system. Regulates dendrite and axon branching and morphogenesis. Promotes the migration of cerebellar granule cells and of endothelial cells. Plays a role in the immune system; induces B-cells to aggregate and improves their viability (in vitro). Promotes signaling via SRC and PTK2B/PYK2, which then mediates activation of phosphatidylinositol 3-kinase and of the AKT1 signaling cascade. Interaction with PLXNB1 mediates activation of RHOA. {ECO:0000269PubMed:16055703, ECO:0000269PubMed:19788569, ECO:0000269PubMed:20877282, ECO:0000269PubMed:8876214}.
Subcellular Localization Cell membrane {ECO:0000269PubMed:20877282, ECO:0000269PubMed:8876214}; Single-pass type I membrane protein {ECO:0000269PubMed:20877282, ECO:0000269PubMed:8876214}.
Disease Associations
Tissue Specificity Strongly expressed in skeletal muscle, peripheral blood lymphocytes, spleen, and thymus and also expressed at lower levels in testes, brain, kidney, small intestine, prostate, heart, placenta, lung and pancreas, but not in colon and liver. {ECO:0000269PubMed:8876214}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 7 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 7 [view]
Protein-Protein 7 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004872 receptor activity
GO:0004888 transmembrane signaling receptor activity
GO:0005102 receptor binding
GO:0005515 protein binding
GO:0030215 semaphorin receptor binding
Biological Process
GO:0000122 negative regulation of transcription from RNA polymerase II promoter
GO:0001934 positive regulation of protein phosphorylation
GO:0006955 immune response
GO:0007155 cell adhesion
GO:0007162 negative regulation of cell adhesion
GO:0007275 multicellular organismal development
GO:0007411 axon guidance
GO:0008360 regulation of cell shape
GO:0010693 negative regulation of alkaline phosphatase activity
GO:0014068 positive regulation of phosphatidylinositol 3-kinase signaling
GO:0030335 positive regulation of cell migration
GO:0031344 regulation of cell projection organization
GO:0032321 positive regulation of Rho GTPase activity
GO:0043066 negative regulation of apoptotic process
GO:0043931 ossification involved in bone maturation
GO:0045668 negative regulation of osteoblast differentiation
GO:0048672 positive regulation of collateral sprouting
GO:0048814 regulation of dendrite morphogenesis
GO:0050731 positive regulation of peptidyl-tyrosine phosphorylation
GO:0050732 negative regulation of peptidyl-tyrosine phosphorylation
GO:0070486 leukocyte aggregation
GO:0071526 semaphorin-plexin signaling pathway
GO:1900220 semaphorin-plexin signaling pathway involved in bone trabecula morphogenesis
Cellular Component
GO:0005615 extracellular space
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0016020 membrane
Protein Structure and Domains
PDB ID
InterPro IPR001627 Sema domain
IPR002165 Plexin
IPR007110 Immunoglobulin-like domain
IPR016201 Plexin-like fold
PFAM PF01403
PF01437
PRINTS
PIRSF
SMART SM00630
SM00423
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q92854
PhosphoSite PhosphoSite-Q92854
TrEMBL F5H044
UniProt Splice Variant
Entrez Gene 10507
UniGene Hs.601897
RefSeq NP_001135759
HUGO HGNC:10732
OMIM 601866
CCDS CCDS47991
HPRD 03520
IMGT
EMBL AK097056 AL590233 AL929575 BC054500 BC137515 BC137518 U60800
GenPept AAC50810 AAH54500 AAI37516 AAI37519 BAC04938 CAI17379 CAI43250 CAI95794