1p9a
From Proteopedia
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{{STRUCTURE_1p9a| PDB=1p9a | SCENE= }} | {{STRUCTURE_1p9a| PDB=1p9a | SCENE= }} | ||
- | + | ===Crystal Structure of N-Terminal Domain of Human Platelet Receptor Glycoprotein Ib-alpha at 1.7 Angstrom Resolution=== | |
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==Disease== | ==Disease== | ||
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[[Category: Leucine rich repeat]] | [[Category: Leucine rich repeat]] | ||
[[Category: Platelet receptor]] | [[Category: Platelet receptor]] | ||
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Revision as of 01:27, 28 July 2008
Contents |
Crystal Structure of N-Terminal Domain of Human Platelet Receptor Glycoprotein Ib-alpha at 1.7 Angstrom Resolution
Template:ABSTRACT PUBMED 12855810
Disease
Known disease associated with this structure: 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
1P9A is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Modulation of alpha-thrombin function by distinct interactions with platelet glycoprotein Ibalpha., Celikel R, McClintock RA, Roberts JR, Mendolicchio GL, Ware J, Varughese KI, Ruggeri ZM, Science. 2003 Jul 11;301(5630):218-21. PMID:12855810
Page seeded by OCA on Mon Jul 28 04:26:52 2008