3bvh

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==About this Structure==
==About this Structure==
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3BVH is a [[Protein complex]] 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=3BVH OCA].
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3BVH is a 10 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=3BVH OCA].
==Reference==
==Reference==
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Polymerization-defective fibrinogen variant gammaD364A binds knob "A" peptide mimic., Bowley SR, Merenbloom BK, Okumura N, Betts L, Heroux A, Gorkun OV, Lord ST, Biochemistry. 2008 Aug 19;47(33):8607-13. Epub 2008 Jul 22. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/18642883 18642883]
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<ref group="xtra">PMID:18642883</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Protein complex]]
 
[[Category: Betts, L.]]
[[Category: Betts, L.]]
[[Category: Bowley, S R.]]
[[Category: Bowley, S R.]]
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[[Category: Sulfation]]
[[Category: Sulfation]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 18:16:42 2009''

Revision as of 16:16, 16 February 2009

Image:3bvh.png

Template:STRUCTURE 3bvh

Contents

Crystal Structure of Recombinant gammaD364A Fibrinogen Fragment D with the Peptide Ligand Gly-Pro-Arg-Pro-Amide

Template:ABSTRACT PUBMED 18642883

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

3BVH is a 10 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  • Bowley SR, Merenbloom BK, Okumura N, Betts L, Heroux A, Gorkun OV, Lord ST. Polymerization-defective fibrinogen variant gammaD364A binds knob "A" peptide mimic. Biochemistry. 2008 Aug 19;47(33):8607-13. Epub 2008 Jul 22. PMID:18642883 doi:10.1021/bi8000769

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