3e1i
From Proteopedia
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Revision as of 05:50, 13 May 2009
Contents |
Crystal Structure of BbetaD432A Variant Fibrinogen Fragment D with the Peptide Ligand Gly-His-Arg-Pro-amide
Template:ABSTRACT PUBMED 19075185
Disease
Known disease associated with this structure: Afibrinogenemia, congenital OMIM:[134820], Amyloidosis, hereditary renal OMIM:[134820], Dysfibrinogenemia, alpha type, causing bleeding diathesis OMIM:[134820], Dysfibrinogenemia, alpha type, causing recurrent thrombosis OMIM:[134820], Afibrinogenemia, congenital OMIM:[134830], Dysfibrinogenemia, beta type OMIM:[134830], Thrombophilia, dysfibrinogenemic OMIM:[134830]
About this Structure
3E1I is a 8 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Bowley SR, Lord ST. Fibrinogen variant BbetaD432A has normal polymerization but does not bind knob "B". Blood. 2009 Apr 30;113(18):4425-30. Epub 2008 Dec 15. PMID:19075185 doi:10.1182/blood-2008-09-178178
Page seeded by OCA on Wed May 13 08:50:35 2009
