1yjt
From Proteopedia
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===Solution structure of the Cu(I) form of the sixth soluble domain A69P mutant of Menkes protein=== | ===Solution structure of the Cu(I) form of the sixth soluble domain A69P mutant of Menkes protein=== | ||
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| - | ==Disease== | ||
| - | 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== | ||
| - | + | [[1yjt]] 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=1YJT OCA]. | |
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| + | ==See Also== | ||
| + | *[[ATPase|ATPase]] | ||
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:016083905</ref><references group="xtra"/> |
[[Category: Copper-exporting ATPase]] | [[Category: Copper-exporting ATPase]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
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[[Category: Rosato, A.]] | [[Category: Rosato, A.]] | ||
[[Category: Wang, S.]] | [[Category: Wang, S.]] | ||
| + | [[Category: Hydrolase]] | ||
[[Category: Metal homeostasis]] | [[Category: Metal homeostasis]] | ||
[[Category: Metallochaperone]] | [[Category: Metallochaperone]] | ||
[[Category: Protein-protein interaction]] | [[Category: Protein-protein interaction]] | ||
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| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Feb 18 01:59:35 2009'' | ||
Revision as of 08:50, 27 July 2012
Contents |
Solution structure of the Cu(I) form of the sixth soluble domain A69P mutant of Menkes protein
Template:ABSTRACT PUBMED 16083905
About this Structure
1yjt 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
