The rapid-onset dystonia parkinsonism mutation D923N of the Na +,K+-ATPase α3 isoform disrupts Na+ interaction at the third Na+ site

Journal of Biological Chemistry

Volumn 285, Issue 34, 2010, Pages 26245-26254

  Einholm, Anja Pernille ^a   Toustrup Jensen, Mads S ^a   Holm, Rikke ^a   Andersen, Jens Peter ^a   Vilsen, Bente ^a  

^a AARHUS UNIVERSITY   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

C TERMINUS; CONFORMATIONAL TRANSITIONS; EXTRACELLULAR; ISOFORMS; NEUROLOGICAL DISORDERS; SITE BINDING; STRUCTURAL MODELING; TRANSMEMBRANE HELICES; TRANSPORT CHANNEL; WILD TYPES;

CALCIUM; ENZYME ACTIVITY; PHOSPHORYLATION;

CRYSTAL STRUCTURE;

ADENOSINE TRIPHOSPHATASE (CALCIUM); ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); ASPARAGINE; SODIUM ION;

ARTICLE; BINDING AFFINITY; CARBOXY TERMINAL SEQUENCE; CELL MEMBRANE; CONTROLLED STUDY; CRYSTAL STRUCTURE; DYSTONIA; ENZYME ACTIVATION; ENZYME ACTIVE SITE; ENZYME PHOSPHORYLATION; ENZYME STRUCTURE; GENE MUTATION; HUMAN; PARKINSONISM; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN INTERACTION; PROTEIN LOCALIZATION; SODIUM CELL LEVEL; SODIUM TRANSPORT;

ANIMALS; BINDING SITES; CERCOPITHECUS AETHIOPS; COS CELLS; DYSTONIC DISORDERS; HUMANS; MUTATION, MISSENSE; PARKINSONIAN DISORDERS; POTASSIUM; PROTEIN BINDING; SODIUM; SODIUM-POTASSIUM-EXCHANGING ATPASE;

HUMAN ECHOVIRUS 1;

EID: 77956197644     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M110.123976     Document Type: Article

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