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1rf0

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Revision as of 12:24, 17 February 2009 by OCA (Talk | contribs)
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Template:STRUCTURE 1rf0

Contents

Crystal Structure of Fragment D of gammaE132A Fibrinogen

Template:ABSTRACT PUBMED 14992585

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], Dysfibrinogenemia, gamma type OMIM:[134850], Hypofibrinogenemia, gamma type OMIM:[134850], Thrombophilia, dysfibrinogenemic OMIM:[134850]

About this Structure

1RF0 is a 6 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  • Kostelansky MS, Lounes KC, Ping LF, Dickerson SK, Gorkun OV, Lord ST. Calcium-binding site beta 2, adjacent to the "b" polymerization site, modulates lateral aggregation of protofibrils during fibrin polymerization. Biochemistry. 2004 Mar 9;43(9):2475-83. PMID:14992585 doi:http://dx.doi.org/10.1021/bi0359978

Page seeded by OCA on Tue Feb 17 14:24:36 2009

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