1dxx: Difference between revisions
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[[Image:1dxx.gif|left|200px]] | [[Image:1dxx.gif|left|200px]] | ||
'''N-TERMINAL ACTIN-BINDING DOMAIN OF HUMAN DYSTROPHIN''' | {{Structure | ||
|PDB= 1dxx |SIZE=350|CAPTION= <scene name='initialview01'>1dxx</scene>, resolution 2.6Å | |||
|SITE= | |||
|LIGAND= | |||
|ACTIVITY= | |||
|GENE= DMD ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]) | |||
}} | |||
'''N-TERMINAL ACTIN-BINDING DOMAIN OF HUMAN DYSTROPHIN''' | |||
==Overview== | ==Overview== | ||
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==About this Structure== | ==About this Structure== | ||
1DXX is a [ | 1DXX is a [[Single protein]] structure of 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== | ||
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:[http:// | 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:[http://www.ncbi.nlm.nih.gov/pubmed/10801490 10801490] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
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[[Category: utrophin]] | [[Category: utrophin]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 10:46:13 2008'' | ||
