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3hus
From Proteopedia
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Revision as of 05:22, 23 September 2009
Contents |
Crystal structure of recombinant gamma N308K fibrinogen fragment D with the peptide ligand Gly-Pro-Arg-Pro-amide
Template:ABSTRACT PUBMED 19650644
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]
About this Structure
3HUS is a 10 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Bowley SR, Okumura N, Lord ST. Impaired protofibril formation in fibrinogen N308K is due to altered D:D and A:a interactions. Biochemistry. 2009 Aug 3. PMID:19650644 doi:10.1021/bi900239b
Page seeded by OCA on Wed Sep 23 08:22:54 2009
Categories: Homo sapiens | Bowley, S R. | Lord, S T. | Okumura, N. | Alternative splicing | Amyloid | Amyloidosis | Blood clotting | Blood coagulation | Calcium | Coiled coil | Disease mutation | Disulfide bond | Fibrinogen fragment d | Glycoprotein | Isopeptide bond | Phosphoprotein | Polymorphism | Pyrrolidone carboxylic acid | Secreted | Sulfation
