1p9a: Difference between revisions

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{{ABSTRACT_PUBMED_12855810}}
{{ABSTRACT_PUBMED_12855810}}
==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==
1P9A is a 1 chain structure of 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=1P9A OCA].  
1P9A is a 1 chain structure 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=1P9A OCA].  


==Reference==
==Reference==
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[[Category: Ruggeri, Z M.]]
[[Category: Ruggeri, Z M.]]
[[Category: Varughese, K I.]]
[[Category: Varughese, K I.]]
[[Category: Blood clotting]]
[[Category: Glycocalicin]]
[[Category: Glycocalicin]]
[[Category: Leucine rich repeat]]
[[Category: Leucine rich repeat]]
[[Category: Platelet receptor]]
[[Category: Platelet receptor]]


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