2ffd
From Proteopedia
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| , resolution 2.890Å | |||||||
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| Ligands: | |||||||
| Gene: | FGA (Homo sapiens), FGB (Homo sapiens), FGG (Homo sapiens) | ||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||
Fibrinogen Fragment D with "A" knob peptide mimic GPRVVE
Disease
Known diseases associated with this structure: Afibrinogenemia, congenital OMIM:[134820], Afibrinogenemia, congenital OMIM:[134830], Amyloidosis, hereditary renal OMIM:[134820], Dysfibrinogenemia, alpha type, causing bleeding diathesis OMIM:[134820], Dysfibrinogenemia, alpha type, causing recurrent thrombosis OMIM:[134820], Dysfibrinogenemia, beta type OMIM:[134830], Dysfibrinogenemia, gamma type OMIM:[134850], Hypofibrinogenemia, gamma type OMIM:[134850], Thrombophilia, dysfibrinogenemic OMIM:[134830], 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 Thu Mar 20 16:51:45 2008
