2KOY
Structure of the E1064A mutant of the N-domain of Wilson Disease Associated Protein
Summary for 2KOY
Entry DOI | 10.2210/pdb2koy/pdb |
Related | 2ARF |
NMR Information | BMRB: 16536 |
Descriptor | Copper-transporting ATPase 2 (1 entity in total) |
Functional Keywords | atp7b, 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 source | Homo sapiens (human) |
Total number of polymer chains | 1 |
Total formula weight | 14752.18 |
Authors | Dmitriev, O.Y. (deposition date: 2009-10-03, release date: 2010-12-15, Last modification date: 2024-05-22) |
Primary citation | Dmitriev, 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: 21398519DOI: 10.1074/jbc.M110.198101 PDB entries with the same primary citation |
Experimental method | SOLUTION NMR |
Structure validation
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