Dystonia-associated forms of TorsinA are deficient in ATPase activity

Journal of Molecular Neuroscience

Volumn 25, Issue 1, 2005, Pages 105-117

  Konakova, Marina ^a,c   Pulst, Stefan M ^a,b  

^a BURNS AND ALLEN RESEARCH INSTITUTE   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c ProteomTech Inc   (United States)

Author keywords

ATPase; Dystonia; Inclusion bodies; Protein refolding; TorsinA

Indexed keywords

ADENOSINE TRIPHOSPHATASE; AMINO ACID; RECOMBINANT PROTEIN; TORSINA PROTEIN; UNCLASSIFIED DRUG; VANADATE SODIUM; ADENOSINE TRIPHOSPHATE; CHAPERONE; DYT1 PROTEIN, HUMAN;

ARTICLE; BACTERIUM; CATALYSIS; CELL INCLUSION; DISEASE ASSOCIATION; DYSTONIA; ENZYME ACTIVITY; ESCHERICHIA COLI; GENE MUTATION; GENE OVEREXPRESSION; HYDROLYSIS; IONIC STRENGTH; PH; PROTEIN EXPRESSION; TEMPERATURE; AMINO ACID SEQUENCE; CHEMISTRY; DRUG ANTAGONISM; ENZYME STABILITY; GENETICS; HUMAN; METABOLISM; MOLECULAR GENETICS; MUTATION; NUCLEOTIDE SEQUENCE; PROTEIN CONFORMATION; PROTEIN FOLDING; TORSION DYSTONIA;

ESCHERICHIA COLI;

ADENOSINE TRIPHOSPHATASES; ADENOSINE TRIPHOSPHATE; AMINO ACID SEQUENCE; BASE SEQUENCE; DYSTONIA MUSCULORUM DEFORMANS; ENZYME STABILITY; HUMANS; MOLECULAR CHAPERONES; MOLECULAR SEQUENCE DATA; MUTATION; PROTEIN CONFORMATION; PROTEIN FOLDING; RECOMBINANT PROTEINS;

EID: 25144442749     PISSN: 08958696     EISSN: None     Source Type: Journal    
DOI: 10.1385/JMN:25:1:105     Document Type: Article

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