Homo sapiens Protein: ITGB3
Summary
InnateDB Protein IDBP-584429.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ITGB3
Protein Name integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
Synonyms BDPLT16; BDPLT2; CD61; GP3A; GPIIIa; GT;
Species Homo sapiens
Ensembl Protein ENSP00000452786
InnateDB Gene IDBG-547297 (ITGB3)
Protein Structure
UniProt Annotation
Function Integrin alpha-V/beta-3 is a receptor for cytotactin, fibronectin, laminin, matrix metalloproteinase-2, osteopontin, osteomodulin, prothrombin, thrombospondin, vitronectin and von Willebrand factor. Integrin alpha-IIb/beta-3 is a receptor for fibronectin, fibrinogen, plasminogen, prothrombin, thrombospondin and vitronectin. Integrins alpha-IIb/beta-3 and alpha-V/beta-3 recognize the sequence R-G-D in a wide array of ligands. Integrin alpha-IIb/beta-3 recognizes the sequence H-H-L-G-G-G-A-K-Q-A-G-D-V in fibrinogen gamma chain. Following activation integrin alpha- IIb/beta-3 brings about platelet/platelet interaction through binding of soluble fibrinogen. This step leads to rapid platelet aggregation which physically plugs ruptured endothelial surface. In case of HIV-1 infection, the interaction with extracellular viral Tat protein seems to enhance angiogenesis in Kaposi's sarcoma lesions.
Subcellular Localization Cell membrane {ECO:0000269PubMed:20702409}; Single-pass type I membrane protein {ECO:0000269PubMed:20702409}. Cell projection, lamellipodium membrane {ECO:0000269PubMed:20702409}. Cell junction, focal adhesion {ECO:0000269PubMed:20702409}.
Disease Associations Glanzmann thrombasthenia (GT) [MIM:273800]: A common inherited disease of platelet aggregation. It is characterized by mucocutaneous bleeding of mild-to-moderate severity. GT has been classified clinically into types I and II. In type I, platelets show absence of the glycoprotein IIb-IIIa complexes at their surface and lack fibrinogen and clot retraction capability. In type II, the platelets express the GPIIb-IIIa complex at reduced levels, have detectable amounts of fibrinogen, and have low or moderate clot retraction capability. {ECO:0000269PubMed:10233432, ECO:0000269PubMed:11588040, ECO:0000269PubMed:11897046, ECO:0000269PubMed:12083483, ECO:0000269PubMed:12353082, ECO:0000269PubMed:1371279, ECO:0000269PubMed:1438206, ECO:0000269PubMed:15583747, ECO:0000269PubMed:15634267, ECO:0000269PubMed:15748237, ECO:0000269PubMed:1602006, ECO:0000269PubMed:20020534, ECO:0000269PubMed:2392682, ECO:0000269PubMed:8781422, ECO:0000269PubMed:9215749, ECO:0000269PubMed:9376589, ECO:0000269PubMed:9684783, ECO:0000269PubMed:9790984}. Note=The disease is caused by mutations affecting the gene represented in this entry.Bleeding disorder, platelet-type 16 (BDPLT16) [MIM:187800]: An autosomal dominant form of congenital macrothrombocytopenia associated with platelet anisocytosis. It is a disorder of platelet production. Affected individuals may have no or only mildly increased bleeding tendency. In vitro studies show mild platelet functional abnormalities. {ECO:0000269PubMed:18065693}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Isoform beta-3A and isoform beta-3C are widely expressed. Isoform beta-3A is specifically expressed in osteoblast cells; isoform beta-3C is specifically expressed in prostate and testis.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 62 experimentally validated interaction(s) in this database.
They are also associated with 11 interaction(s) predicted by orthology.
Experimentally validated
Total 62 [view]
Protein-Protein 62 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 11 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003756 protein disulfide isomerase activity
GO:0004872 receptor activity
GO:0005161 platelet-derived growth factor receptor binding
GO:0005515 protein binding
GO:0042802 identical protein binding
GO:0043184 vascular endothelial growth factor receptor 2 binding
GO:0050839 cell adhesion molecule binding
Biological Process
GO:0001934 positive regulation of protein phosphorylation
GO:0001938 positive regulation of endothelial cell proliferation
GO:0002576 platelet degranulation
GO:0006457 protein folding
GO:0007044 cell-substrate junction assembly
GO:0007155 cell adhesion
GO:0007160 cell-matrix adhesion
GO:0007229 integrin-mediated signaling pathway
GO:0007275 multicellular organismal development
GO:0007411 axon guidance
GO:0007596 blood coagulation
GO:0010595 positive regulation of endothelial cell migration
GO:0010745 negative regulation of macrophage derived foam cell differentiation
GO:0010888 negative regulation of lipid storage
GO:0014909 smooth muscle cell migration
GO:0016032 viral process
GO:0030168 platelet activation
GO:0030198 extracellular matrix organization
GO:0030949 positive regulation of vascular endothelial growth factor receptor signaling pathway
GO:0031589 cell-substrate adhesion
GO:0032147 activation of protein kinase activity
GO:0032369 negative regulation of lipid transport
GO:0035295 tube development
GO:0042060 wound healing
GO:0045087 innate immune response (InnateDB)
GO:0045124 regulation of bone resorption
GO:0045715 negative regulation of low-density lipoprotein particle receptor biosynthetic process
GO:0050731 positive regulation of peptidyl-tyrosine phosphorylation
GO:0050748 negative regulation of lipoprotein metabolic process
GO:0050900 leukocyte migration
GO:0060055 angiogenesis involved in wound healing
GO:0070527 platelet aggregation
Cellular Component
GO:0005634 nucleus
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0005925 focal adhesion
GO:0008305 integrin complex
GO:0009986 cell surface
GO:0016020 membrane
GO:0031092 platelet alpha granule membrane
GO:0031258 lamellipodium membrane
GO:0042470 melanosome
GO:0043235 receptor complex
GO:0070062 extracellular vesicular exosome
GO:0071062 alphav-beta3 integrin-vitronectin complex
Protein Structure and Domains
PDB ID
InterPro IPR002035 von Willebrand factor, type A
IPR002369 Integrin beta subunit, N-terminal
IPR012896 Integrin beta subunit, tail
IPR013111 EGF-like domain, extracellular
IPR014836 Integrin beta subunit, cytoplasmic domain
IPR015812 Integrin beta subunit
IPR016201 Plexin-like fold
PFAM PF00092
PF00362
PF07965
PF07974
PF08725
PRINTS PR01186
PIRSF PIRSF002512
SMART SM00327
SM00187
SM00423
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P05106
PhosphoSite PhosphoSite-P05106
TrEMBL F2X0V0
UniProt Splice Variant
Entrez Gene 3690
UniGene Hs.732035
RefSeq NP_000203
HUGO HGNC:6156
OMIM 173470
CCDS CCDS11511
HPRD 01428
IMGT
EMBL BC127666 BC127667 CH471231 HQ202730 HQ202731 HQ202732 HQ202734 HQ202735 HQ288894 J02703 KJ189224 L28832 M20311 M25108 M32667 M32672 M32673 M32674 M32675 M32680 M32681 M32682 M32685 M32686 M35999 M57481 M57482 M57483 M57484 M57485 M57486 M57487 M57488 M57489 M57490 M57491 M57492 M57493 M57494 S49379 U03881 U95204
GenPept AAA16076 AAA20880 AAA35927 AAA36121 AAA52589 AAA52600 AAA60122 AAA67537 AAB23689 AAB71380 AAI27667 AAI27668 ADZ28535 ADZ28536 ADZ28537 ADZ28538 ADZ28539 ADZ76020 AHV90406 EAW57682