3hus: Difference between revisions
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Revision as of 05:22, 23 September 2009
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
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- 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
