1re4
From Proteopedia
Contents |
Crystal Structure of Fragment D of BbetaD398A Fibrinogen
Template:ABSTRACT PUBMED 14992584
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
1RE4 is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
B beta Glu397 and B beta Asp398 but not B beta Asp432 are required for "B:b" interactions., Kostelansky MS, Bolliger-Stucki B, Betts L, Gorkun OV, Lord ST, Biochemistry. 2004 Mar 9;43(9):2465-74. PMID:14992584
Page seeded by OCA on Tue Jul 29 12:36:58 2008
