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3e1i

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[[Image:3e1i.png|left|200px]]
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{{ABSTRACT_PUBMED_19075185}}
{{ABSTRACT_PUBMED_19075185}}
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==Disease==
 
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Known disease associated with this structure: Afibrinogenemia, congenital OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134820 134820]], Amyloidosis, hereditary renal OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134820 134820]], Dysfibrinogenemia, alpha type, causing bleeding diathesis OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134820 134820]], Dysfibrinogenemia, alpha type, causing recurrent thrombosis OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134820 134820]], Afibrinogenemia, congenital OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134830 134830]], Dysfibrinogenemia, beta type OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134830 134830]], Thrombophilia, dysfibrinogenemic OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134830 134830]]
 
==About this Structure==
==About this Structure==
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3E1I is a 8 chains structure of sequences 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=3E1I OCA].
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[[3e1i]] is a 8 chain structure of [[Fibrinogen]] 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=3E1I OCA].
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==See Also==
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*[[Fibrinogen]]
==Reference==
==Reference==
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[[Category: Secreted]]
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[[Category: Sulfation]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed May 13 08:50:35 2009''
 

Revision as of 22:17, 26 December 2010

Template:STRUCTURE 3e1i

Contents

Crystal Structure of BbetaD432A Variant Fibrinogen Fragment D with the Peptide Ligand Gly-His-Arg-Pro-amide

Template:ABSTRACT PUBMED 19075185

About this Structure

3e1i is a 8 chain structure of Fibrinogen with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See Also

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

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