Platelet glycoprotein

From Proteopedia

(Redirected from Platelet-receptor glycoprotein Ib alpha)

Platelet-receptor glycoprotein Ib alpha (blue) involved in Willebrand disease bound to the von Willebrand Factor A1 Domain (green surface), (1m10)

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Crystal structure of the complex of Glycoprotein Ib alpha and the von Willebrand Factor A1 Domain

Publication Abstract from PubMed

Transient interactions of platelet-receptor glycoprotein Ibalpha (GpIbalpha) and the plasma protein von Willebrand factor (VWF) reduce platelet velocity at sites of vascular damage and play a role in haemostasis and thrombosis. Here we present structures of the GpIbalpha amino-terminal domain and its complex with the VWF domain A1. In the complex, GpIbalpha wraps around one side of A1, providing two contact areas bridged by an area of solvated charge interaction. The structures explain the effects of gain-of-function mutations related to bleeding disorders and provide a model for shear-induced activation. These detailed insights into the initial interactions in platelet adhesion are relevant to the development of antithrombotic drugs.

Structures of glycoprotein Ibalpha and its complex with von Willebrand factor A1 domain., Huizinga EG, Tsuji S, Romijn RA, Schiphorst ME, de Groot PG, Sixma JJ, Gros P, Science. 2002 Aug 16;297(5584):1176-9. PMID:12183630

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

Platelet glycoprotein Ib alpha has a role in the adhesion and migration of leukocytes on vascular thrombus^[1].
Platelet glycoprotein 4 or CD36 functions as a receptor for thrombospondin and collagen ^[2].
Platelet glycoprotein 6 ha a role in collagen-induced platelet activation^[3].

Disease

Known disease associated with this structure: von Willebrand disease, autosomal dominant OMIM:[193400], von Willebrand disease, autosomal recessive OMIM:[193400], Bernard-Soulier syndrome, benign autosomal dominant OMIM:[606672], Bernard-Soulier syndrome, type A OMIM:[606672], von Willebrand disease, platelet-type OMIM:[606672], Nonarteritic anterior ischemic optic neuropathy, susceptibility to OMIM:[606672]

About this Structure

1m10 is a 2 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

3D structures of platelet glycoprotein

Updated on 21-July-2024

Reference

Huizinga EG, Tsuji S, Romijn RA, Schiphorst ME, de Groot PG, Sixma JJ, Gros P. Structures of glycoprotein Ibalpha and its complex with von Willebrand factor A1 domain. Science. 2002 Aug 16;297(5584):1176-9. PMID:12183630 doi:10.1126/science.107355

↑ Simon DI, Chen Z, Xu H, Li CQ, Dong Jf, McIntire LV, Ballantyne CM, Zhang L, Furman MI, Berndt MC, López JA. Platelet glycoprotein ibalpha is a counterreceptor for the leukocyte integrin Mac-1 (CD11b/CD18). J Exp Med. 2000 Jul 17;192(2):193-204. PMID:10899906 doi:10.1084/jem.192.2.193
↑ Kunicki TJ. Platelet membrane glycoproteins and their function: an overview. Blut. 1989 Jul;59(1):30-4. PMID:2665870
↑ Moroi M, Jung SM. Platelet glycoprotein VI: its structure and function. Thromb Res. 2004;114(4):221-33. PMID:15381385 doi:10.1016/j.thromres.2004.06.046

Proteopedia Page Contributors and Editors (what is this?)

Michal Harel, Alexander Berchansky, Joel L. Sussman, Wayne Decatur, Jaime Prilusky

Retrieved from "http://proteopedia.org/wiki/index.php/Platelet_glycoprotein"

Platelet glycoprotein

From Proteopedia

Crystal structure of the complex of Glycoprotein Ib alpha and the von Willebrand Factor A1 Domain

Disease

About this Structure

3D structures of platelet glycoprotein

Reference

See Also

Proteopedia Page Contributors and Editors (what is this?)

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