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3e1i
From Proteopedia
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
Fibrinogen variant B{beta}D432A has normal polymerization but does not bind knob "B", Bowley SR, Lord ST, Blood. 2008 Dec 15. PMID:19075185
Page seeded by OCA on Wed Jan 14 13:04:42 2009
