1dxx
From Proteopedia
(Difference between revisions)
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==About this Structure== | ==About this Structure== | ||
| - | 1DXX is a | + | 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]. |
==Reference== | ==Reference== | ||
| - | + | <ref group="xtra">PMID:10801490</ref><references group="xtra"/> | |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
| - | [[Category: Single protein]] | ||
[[Category: Keep, N H.]] | [[Category: Keep, N H.]] | ||
[[Category: Kendrick-Jones, J.]] | [[Category: Kendrick-Jones, J.]] | ||
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[[Category: Utrophin]] | [[Category: Utrophin]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 08:00:11 2009'' |
Revision as of 06:00, 17 February 2009
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 4 chains structure of sequences 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
Page seeded by OCA on Tue Feb 17 08:00:11 2009
