2ffd: Difference between revisions

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{{Seed}}
[[Image:2ffd.png|left|200px]]
[[Image:2ffd.png|left|200px]]


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{{STRUCTURE_2ffd|  PDB=2ffd  |  SCENE=  }}  
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==Disease==
==About this Structure==
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]], Dysfibrinogenemia, gamma type OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134850 134850]], Hypofibrinogenemia, gamma type OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134850 134850]], Thrombophilia, dysfibrinogenemic OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134850 134850]]
[[2ffd]] is a 10 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=2FFD OCA].  


==About this Structure==
==See Also==
2FFD 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=2FFD OCA].
*[[Fibrinogen|Fibrinogen]]


==Reference==
==Reference==
<ref group="xtra">PMID:16689770</ref><references group="xtra"/>
<ref group="xtra">PMID:016689770</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Betts, L.]]
[[Category: Betts, L.]]
[[Category: Blood clotting]]
[[Category: Complex of fibrinogen with a site mimic gprvve in both a and b site]]
[[Category: Complex of fibrinogen with a site mimic gprvve in both a and b site]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 09:04:36 2009''

Revision as of 12:20, 26 July 2012

File:2ffd.png

Template:STRUCTURE 2ffd

Fibrinogen Fragment D with "A" knob peptide mimic GPRVVE

About this Structure

2ffd is a 10 chain structure of Fibrinogen with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See Also

Reference

  1. Betts L, Merenbloom BK, Lord ST. The structure of fibrinogen fragment D with the 'A' knob peptide GPRVVE. J Thromb Haemost. 2006 May;4(5):1139-41. PMID:16689770 doi:10.1111/j.1538-7836.2006.01902.x

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