Bos taurus Protein: ITGB2 | |||||||||||||||
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Summary | |||||||||||||||
InnateDB Protein | IDBP-691797.2 | ||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||
Gene Symbol | ITGB2 | ||||||||||||||
Protein Name | Integrin beta-2 | ||||||||||||||
Synonyms | |||||||||||||||
Species | Bos taurus | ||||||||||||||
Ensembl Protein | ENSBTAP00000022687 | ||||||||||||||
InnateDB Gene | IDBG-639611 (ITGB2) | ||||||||||||||
Protein Structure | |||||||||||||||
UniProt Annotation | |||||||||||||||
Function | Triggers neutrophil transmigration during lung injury through PTK2B/PYK2-mediated activation (By similarity). Integrin alpha-L/beta-2 is a receptor for ICAM1, ICAM2, ICAM3 and ICAM4. Integrins alpha-M/beta-2 and alpha-X/beta-2 are receptors for the iC3b fragment of the third complement component and for fibrinogen. Integrin alpha-X/beta-2 recognizes the sequence G-P-R in fibrinogen alpha-chain. Integrin alpha-M/beta-2 recognizes P1 and P2 peptides of fibrinogen gamma chain. Integrin alpha-M/beta-2 is also a receptor for factor X. Integrin alpha-D/beta-2 is a receptor for ICAM3 and VCAM1. {ECO:0000250}. | ||||||||||||||
Subcellular Localization | Membrane; Single-pass type I membrane protein. | ||||||||||||||
Disease Associations | Note=Defects in ITGB2 are the cause of leukocyte adhesion deficiency (LAD). The mutation causing LAD (Gly-128) is prevalent among Holstein cattle throughout the world, placing this disorder among the most common genetic diseases known in animal agriculture. All cattle with the mutant allele are related to one bull, who through the use of artificial insemination sired many calves in the 1950s and 1960s. | ||||||||||||||
Tissue Specificity | |||||||||||||||
Comments | |||||||||||||||
Interactions | |||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 35 interaction(s) predicted by orthology.
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Gene Ontology | |||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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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 |
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PFAM |
PF00092
PF00362 PF07965 PF07974 PF08725 |
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PRINTS |
PR01186
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PIRSF |
PIRSF002512
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SMART |
SM00327
SM00187 SM00423 |
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TIGRFAMs | |||||||||||||||
Post-translational Modifications | |||||||||||||||
Modification | |||||||||||||||
Cross-References | |||||||||||||||
SwissProt | P32592 | ||||||||||||||
PhosphoSite | PhosphoSite- | ||||||||||||||
TrEMBL | Q9N0Y4 | ||||||||||||||
UniProt Splice Variant | |||||||||||||||
Entrez Gene | 281877 | ||||||||||||||
UniGene | Bt.63143 | ||||||||||||||
RefSeq | NP_786975 | ||||||||||||||
HUGO | |||||||||||||||
OMIM | |||||||||||||||
CCDS | |||||||||||||||
HPRD | |||||||||||||||
IMGT | |||||||||||||||
EMBL | AF239220 FJ853493 KF840683 M81233 Y12672 | ||||||||||||||
GenPept | AAA30438 AAF64158 ACQ83645 AHD24932 CAA73212 | ||||||||||||||