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1yju

From Proteopedia

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{{Seed}}
 
[[Image:1yju.png|left|200px]]
[[Image:1yju.png|left|200px]]
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{{ABSTRACT_PUBMED_16083905}}
{{ABSTRACT_PUBMED_16083905}}
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==Disease==
 
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Known disease associated with this structure: Cutis laxa, neonatal OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300011 300011]], Menkes disease OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300011 300011]], Occipital horn syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300011 300011]]
 
==About this Structure==
==About this Structure==
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1YJU is a 1 chain structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1YJU OCA].
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[[1yju]] is a 1 chain structure of [[ATPase]] with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1YJU OCA].
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==See Also==
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*[[ATPase]]
==Reference==
==Reference==
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[[Category: SPINE, Structural Proteomics in Europe.]]
[[Category: SPINE, Structural Proteomics in Europe.]]
[[Category: Wang, S.]]
[[Category: Wang, S.]]
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[[Category: Hydrolase]]
[[Category: Metal homeostasis]]
[[Category: Metal homeostasis]]
[[Category: Metallochaperone]]
[[Category: Metallochaperone]]
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[[Category: Structural genomic]]
[[Category: Structural genomic]]
[[Category: Structural proteomics in europe]]
[[Category: Structural proteomics in europe]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 19:50:05 2009''
 

Revision as of 08:08, 26 December 2010

Image:1yju.png

Template:STRUCTURE 1yju

Contents

Solution structure of the apo form of the sixth soluble domain of Menkes protein

Template:ABSTRACT PUBMED 16083905

About this Structure

1yju is a 1 chain structure of ATPase with sequence from Homo sapiens. Full experimental information is available from OCA.

See Also

Reference

  • Banci L, Bertini I, Cantini F, Migliardi M, Rosato A, Wang S. An atomic-level investigation of the disease-causing A629P mutant of the Menkes protein, ATP7A. J Mol Biol. 2005 Sep 16;352(2):409-17. PMID:16083905 doi:10.1016/j.jmb.2005.07.034

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OCA

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