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3bvh
From Proteopedia
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 Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
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:18642883
Page seeded by OCA on Wed Sep 3 13:08:50 2008
Categories: Homo sapiens | Protein complex | Betts, L. | Bowley, S R. | Gorkun, O V. | Heroux, A. | Lord, S T. | Merenbloom, B K. | Okumura, N. | Alternative splicing | Blood clotting | Blood coagulation | Calcium | Coiled coil | Disease mutation | Glycoprotein | Phosphoprotein | Polymorphism | Pyrrolidone carboxylic acid | Secreted | Sulfation
