1sq0
From Proteopedia
(Difference between revisions)
| Line 1: | Line 1: | ||
| - | {{Seed}} | ||
[[Image:1sq0.png|left|200px]] | [[Image:1sq0.png|left|200px]] | ||
| - | <!-- | ||
| - | The line below this paragraph, containing "STRUCTURE_1sq0", creates the "Structure Box" on the page. | ||
| - | You may change the PDB parameter (which sets the PDB file loaded into the applet) | ||
| - | or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | ||
| - | or leave the SCENE parameter empty for the default display. | ||
| - | --> | ||
{{STRUCTURE_1sq0| PDB=1sq0 | SCENE= }} | {{STRUCTURE_1sq0| PDB=1sq0 | SCENE= }} | ||
===Crystal Structure of the Complex of the Wild-type Von Willebrand Factor A1 domain and Glycoprotein Ib alpha at 2.6 Angstrom Resolution=== | ===Crystal Structure of the Complex of the Wild-type Von Willebrand Factor A1 domain and Glycoprotein Ib alpha at 2.6 Angstrom Resolution=== | ||
| - | |||
| - | <!-- | ||
| - | The line below this paragraph, {{ABSTRACT_PUBMED_15039442}}, adds the Publication Abstract to the page | ||
| - | (as it appears on PubMed at http://www.pubmed.gov), where 15039442 is the PubMed ID number. | ||
| - | --> | ||
{{ABSTRACT_PUBMED_15039442}} | {{ABSTRACT_PUBMED_15039442}} | ||
| - | |||
| - | ==Disease== | ||
| - | Known disease associated with this structure: Bernard-Soulier syndrome, benign autosomal dominant OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606672 606672]], Bernard-Soulier syndrome, type A OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606672 606672]], von Willebrand disease, platelet-type OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606672 606672]], Nonarteritic anterior ischemic optic neuropathy, susceptibility to OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606672 606672]] | ||
==About this Structure== | ==About this Structure== | ||
| - | + | [[1sq0]] is a 2 chain structure of [[Platelet-receptor glycoprotein Ib alpha]] with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1SQ0 OCA]. | |
| + | |||
| + | ==See Also== | ||
| + | *[[Platelet-receptor glycoprotein Ib alpha|Platelet-receptor glycoprotein Ib alpha]] | ||
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:015039442</ref><references group="xtra"/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Dumas, J J.]] | [[Category: Dumas, J J.]] | ||
| Line 35: | Line 23: | ||
[[Category: Stahl, M L.]] | [[Category: Stahl, M L.]] | ||
[[Category: Sullivan, F.]] | [[Category: Sullivan, F.]] | ||
| - | + | [[Category: Blood clotting]] | |
| - | + | ||
Revision as of 01:57, 27 July 2012
Contents |
Crystal Structure of the Complex of the Wild-type Von Willebrand Factor A1 domain and Glycoprotein Ib alpha at 2.6 Angstrom Resolution
Template:ABSTRACT PUBMED 15039442
About this Structure
1sq0 is a 2 chain structure of Platelet-receptor glycoprotein Ib alpha with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Dumas JJ, Kumar R, McDonagh T, Sullivan F, Stahl ML, Somers WS, Mosyak L. Crystal structure of the wild-type von Willebrand factor A1-glycoprotein Ibalpha complex reveals conformation differences with a complex bearing von Willebrand disease mutations. J Biol Chem. 2004 May 28;279(22):23327-34. Epub 2004 Mar 23. PMID:15039442 doi:10.1074/jbc.M401659200
