Glycoprotein IX
From Wikipedia, the free encyclopedia
Glycoprotein IX (platelet)
|
||||||||||||||
Identifiers | ||||||||||||||
Symbol(s) | GP9; CD42a; GPIX | |||||||||||||
External IDs | OMIM: 173515 MGI: 1860137 HomoloGene: 144 | |||||||||||||
|
||||||||||||||
RNA expression pattern | ||||||||||||||
Orthologs | ||||||||||||||
Human | Mouse | |||||||||||||
Entrez | 2815 | 54368 | ||||||||||||
Ensembl | ENSG00000169704 | ENSMUSG00000030054 | ||||||||||||
Uniprot | P14770 | n/a | ||||||||||||
Refseq | NM_000174 (mRNA) NP_000165 (protein) |
NM_018762 (mRNA) NP_061232 (protein) |
||||||||||||
Location | Chr 3: 130.26 - 130.26 Mb | Chr 6: 87.74 - 87.75 Mb | ||||||||||||
Pubmed search | [1] | [2] |
Glycoprotein IX (platelet) (GP9) also known as CD42a (Cluster of Differentiation 42a), is a human gene.[1]
Platelet glycoprotein IX (GP9) is a small membrane glycoprotein found on the surface of human platelets. It forms a 1-to-1 noncovalent complex with glycoprotein Ib (GP Ib), a platelet surface membrane glycoprotein complex that functions as a receptor for von Willebrand factor (VWF; MIM 193400). The main portion of the receptor is a heterodimer composed of 2 polypeptide chains, an alpha chain (GP1BA; MIM 606672) and a beta chain (GP1BB; MIM 138720), that are linked by disulfide bonds. The complete receptor complex includes noncovalent association of the alpha and beta subunits with GP9 and platelet glycoprotein V (GP5; MIM 173511).[supplied by OMIM][1]
Contents |
[edit] See also
[edit] References
[edit] Further reading
- Kunishima S, Kamiya T, Saito H (2003). "Genetic abnormalities of Bernard-Soulier syndrome.". Int. J. Hematol. 76 (4): 319-27. PMID 12463594.
- Hickey MJ, Deaven LL, Roth GJ (1991). "Human platelet glycoprotein IX. Characterization of cDNA and localization of the gene to chromosome 3.". FEBS Lett. 274 (1-2): 189-92. PMID 2253772.
- Du X, Beutler L, Ruan C, et al. (1987). "Glycoprotein Ib and glycoprotein IX are fully complexed in the intact platelet membrane.". Blood 69 (5): 1524-7. PMID 2436691.
- Andrews RK, Booth WJ, Gorman JJ, et al. (1990). "Purification of botrocetin from Bothrops jararaca venom. Analysis of the botrocetin-mediated interaction between von Willebrand factor and the human platelet membrane glycoprotein Ib-IX complex.". Biochemistry 28 (21): 8317-26. PMID 2557900.
- Hickey MJ, Williams SA, Roth GJ (1989). "Human platelet glycoprotein IX: an adhesive prototype of leucine-rich glycoproteins with flank-center-flank structures.". Proc. Natl. Acad. Sci. U.S.A. 86 (17): 6773-7. PMID 2771955.
- Roth GJ, Ozols J, Nugent DJ, Williams SA (1988). "Isolation and characterization of human platelet glycoprotein IX.". Biochem. Biophys. Res. Commun. 156 (2): 931-9. PMID 3056407.
- Meyer SC, Fox JE (1995). "Interaction of platelet glycoprotein V with glycoprotein Ib-IX regulates expression of the glycoproteins and binding of von Willebrand factor to glycoprotein Ib-IX in transfected cells.". J. Biol. Chem. 270 (24): 14693-9. PMID 7782333.
- Clemetson JM, Kyrle PA, Brenner B, Clemetson KJ (1994). "Variant Bernard-Soulier syndrome associated with a homozygous mutation in the leucine-rich domain of glycoprotein IX.". Blood 84 (4): 1124-31. PMID 8049428.
- Hickey MJ, Roth GJ (1993). "Characterization of the gene encoding human platelet glycoprotein IX.". J. Biol. Chem. 268 (5): 3438-43. PMID 8429020.
- Wright SD, Michaelides K, Johnson DJ, et al. (1993). "Double heterozygosity for mutations in the platelet glycoprotein IX gene in three siblings with Bernard-Soulier syndrome.". Blood 81 (9): 2339-47. PMID 8481514.
- Berger G, Massé JM, Cramer EM (1996). "Alpha-granule membrane mirrors the platelet plasma membrane and contains the glycoproteins Ib, IX, and V.". Blood 87 (4): 1385-95. PMID 8608228.
- Hollmann C, Haag F, Schlott M, et al. (1996). "Molecular characterization of mouse T-cell ecto-ADP-ribosyltransferase Rt6: cloning of a second functional gene and identification of the Rt6 gene products.". Mol. Immunol. 33 (9): 807-17. PMID 8811076.
- Noris P, Simsek S, Stibbe J, von dem Borne AE (1997). "A phenylalanine-55 to serine amino-acid substitution in the human glycoprotein IX leucine-rich repeat is associated with Bernard-Soulier syndrome.". Br. J. Haematol. 97 (2): 312-20. PMID 9163595.
- Hayashi T, Suzuki K, Yahagi A, et al. (1997). "Corrected DNA sequence of the platelet glycoprotein IX gene.". Thromb. Haemost. 77 (5): 1034-5. PMID 9184424.
- Bradford HN, Dela Cadena RA, Kunapuli SP, et al. (1997). "Human kininogens regulate thrombin binding to platelets through the glycoprotein Ib-IX-V complex.". Blood 90 (4): 1508-15. PMID 9269768.
- Suzuki K, Hayashi T, Yahagi A, et al. (1998). "Novel point mutation in the leucine-rich motif of the platelet glycoprotein IX associated with Bernard-Soulier syndrome.". Br. J. Haematol. 99 (4): 794-800. PMID 9432024.
- Noris P, Arbustini E, Spedini P, et al. (1999). "A new variant of Bernard-Soulier syndrome characterized by dysfunctional glycoprotein (GP) Ib and severely reduced amounts of GPIX and GPV.". Br. J. Haematol. 103 (4): 1004-13. PMID 9886312.
- Longhurst CM, White MM, Wilkinson DA, Jennings LK (1999). "A CD9, alphaIIbbeta3, integrin-associated protein, and GPIb/V/IX complex on the surface of human platelets is influenced by alphaIIbbeta3 conformational states.". Eur. J. Biochem. 263 (1): 104-11. PMID 10429193.
- Kunishima S, Tomiyama Y, Honda S, et al. (2000). "Cys97-->Tyr mutation in the glycoprotein IX gene associated with Bernard-Soulier syndrome.". Br. J. Haematol. 107 (3): 539-45. PMID 10583255.
- Rivera CE, Villagra J, Riordan M, et al. (2001). "Identification of a new mutation in platelet glycoprotein IX (GPIX) in a patient with Bernard-Soulier syndrome.". Br. J. Haematol. 112 (1): 105-8. PMID 11167791.
[edit] External links
This article incorporates text from the United States National Library of Medicine, which is in the public domain.