1dxx
From Proteopedia
Contents |
N-TERMINAL ACTIN-BINDING DOMAIN OF HUMAN DYSTROPHIN
Template:ABSTRACT PUBMED 10801490
Disease
Known disease associated with this structure: Becker muscular dystrophy OMIM:[300377], Cardiomyopathy, dilated, 3B OMIM:[300377], Duchenne muscular dystrophy OMIM:[300377]
About this Structure
1DXX is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
The structure of the N-terminal actin-binding domain of human dystrophin and how mutations in this domain may cause Duchenne or Becker muscular dystrophy., Norwood FL, Sutherland-Smith AJ, Keep NH, Kendrick-Jones J, Structure. 2000 May 15;8(5):481-91. PMID:10801490
Page seeded by OCA on Mon Jun 30 23:47:12 2008
