1dxx: Difference between revisions

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{{Seed}}
[[Image:1dxx.png|left|200px]]
[[Image:1dxx.png|left|200px]]


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{{STRUCTURE_1dxx|  PDB=1dxx  |  SCENE=  }}  
{{STRUCTURE_1dxx|  PDB=1dxx  |  SCENE=  }}  


===N-TERMINAL ACTIN-BINDING DOMAIN OF HUMAN DYSTROPHIN===
===N-TERMINAL ACTIN-BINDING DOMAIN OF HUMAN DYSTROPHIN===


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{{ABSTRACT_PUBMED_10801490}}
{{ABSTRACT_PUBMED_10801490}}
==Disease==
Known disease associated with this structure: Becker muscular dystrophy OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300377 300377]], Cardiomyopathy, dilated, 3B OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300377 300377]], Duchenne muscular dystrophy OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300377 300377]]


==About this Structure==
==About this Structure==
1DXX is a 4 chains structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1DXX OCA].  
[[1dxx]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1DXX OCA].  


==Reference==
==Reference==
<ref group="xtra">PMID:10801490</ref><references group="xtra"/>
<ref group="xtra">PMID:010801490</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Keep, N H.]]
[[Category: Keep, N H.]]
Line 36: Line 21:
[[Category: Dystrophin]]
[[Category: Dystrophin]]
[[Category: Muscular dystrophy]]
[[Category: Muscular dystrophy]]
[[Category: Structural protein]]
[[Category: Utrophin]]
[[Category: Utrophin]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 08:00:11 2009''

Revision as of 09:56, 31 October 2012

Template:STRUCTURE 1dxx

N-TERMINAL ACTIN-BINDING DOMAIN OF HUMAN DYSTROPHIN

Template:ABSTRACT PUBMED 10801490

About this Structure

1dxx is a 4 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  1. Norwood FL, Sutherland-Smith AJ, Keep NH, Kendrick-Jones J. 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. Structure. 2000 May 15;8(5):481-91. PMID:10801490

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