1yjt

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Image:1yjt.png

Template:STRUCTURE 1yjt

Contents

Solution structure of the Cu(I) form of the sixth soluble domain A69P mutant of Menkes protein

Template:ABSTRACT PUBMED 16083905

Disease

Known disease associated with this structure: Cutis laxa, neonatal OMIM:[300011], Menkes disease OMIM:[300011], Occipital horn syndrome OMIM:[300011]

About this Structure

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

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

Page seeded by OCA on Wed Feb 18 01:59:35 2009

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