2ffd
From Proteopedia
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[[Image:2ffd.gif|left|200px]] | [[Image:2ffd.gif|left|200px]] | ||
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'''Fibrinogen Fragment D with "A" knob peptide mimic GPRVVE''' | '''Fibrinogen Fragment D with "A" knob peptide mimic GPRVVE''' | ||
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[[Category: Protein complex]] | [[Category: Protein complex]] | ||
[[Category: Betts, L.]] | [[Category: Betts, L.]] | ||
| - | [[Category: | + | [[Category: Complex of fibrinogen with a site mimic gprvve in both a and b site]] |
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Revision as of 00:49, 4 May 2008
Fibrinogen Fragment D with "A" knob peptide mimic GPRVVE
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
2FFD is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
The structure of fibrinogen fragment D with the 'A' knob peptide GPRVVE., Betts L, Merenbloom BK, Lord ST, J Thromb Haemost. 2006 May;4(5):1139-41. PMID:16689770 Page seeded by OCA on Sun May 4 03:49:53 2008
