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2KOY

Structure of the E1064A mutant of the N-domain of Wilson Disease Associated Protein

Summary for 2KOY
Entry DOI10.2210/pdb2koy/pdb
Related2ARF
NMR InformationBMRB: 16536
DescriptorCopper-transporting ATPase 2 (1 entity in total)
Functional Keywordsatp7b, wilson disease, atpase, copper transport, atp binding, atp-binding, disease mutation, golgi apparatus, hydrolase, ion transport, magnesium, membrane, metal-binding, mitochondrion, nucleotide-binding, phosphoprotein, transmembrane, transport, metal transport
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight14752.18
Authors
Dmitriev, O.Y. (deposition date: 2009-10-03, release date: 2010-12-15, Last modification date: 2021-10-13)
Primary citationDmitriev, O.Y.,Bhattacharjee, A.,Nokhrin, S.,Uhlemann, E.M.,Lutsenko, S.
Difference in stability of the N-domain underlies distinct intracellular properties of the E1064A and H1069Q mutants of copper-transporting ATPase ATP7B.
J. Biol. Chem., 286:16355-16362, 2011
Cited by
PubMed: 21398519
DOI: 10.1074/jbc.M110.198101
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

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