1yjt
From Proteopedia
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 Single protein structure of sequence from Homo sapiens. Full experimental information is available from OCA.
Reference
An atomic-level investigation of the disease-causing A629P mutant of the Menkes protein, ATP7A., Banci L, Bertini I, Cantini F, Migliardi M, Rosato A, Wang S, J Mol Biol. 2005 Sep 16;352(2):409-17. PMID:16083905
Page seeded by OCA on Tue Jul 29 08:51:12 2008
