1dxx
From Proteopedia
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[[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}} | ||
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| - | ==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 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: | + | <ref group="xtra">PMID:010801490</ref><references group="xtra"/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Keep, N H.]] | [[Category: Keep, N H.]] | ||
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[[Category: Dystrophin]] | [[Category: Dystrophin]] | ||
[[Category: Muscular dystrophy]] | [[Category: Muscular dystrophy]] | ||
| + | [[Category: Structural protein]] | ||
[[Category: Utrophin]] | [[Category: Utrophin]] | ||
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| - | ''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
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
- 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
