Copper-regulated trafficking of the Menkes disease copper ATPase is associated with formation of a phosphorylated catalytic intermediate

Journal of Biological Chemistry

Volumn 277, Issue 48, 2002, Pages 46736-46742

  Petris, Michael J ^a   Voskoboinik, Ilia ^b   Cater, Michael ^c   Smith, Kathryn ^a   Kim, Byung Eun ^a   Llanos, Roxana M ^c   Strausak, Daniel ^c   Camakaris, James ^b   Mercer, Julian F B ^c  

^a University of Missouri   (United States)

^b UNIVERSITY OF MELBOURNE   (Australia)

^c DEAKIN UNIVERSITY   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINETRIPHOSPHATE; BIOSYNTHESIS; CATALYSIS; COPPER; ENZYMES;

DEFICIENCY DISORDERS;

BIOCHEMISTRY;

ADENOSINE TRIPHOSPHATASE; COPPER; PHOSPHATASE;

ANIMAL CELL; ARTICLE; CELL MEMBRANE TRANSPORT; CONTROLLED STUDY; ENZYME LOCALIZATION; ENZYME MECHANISM; ENZYME PHOSPHORYLATION; GENE MUTATION; GENETIC CONSERVATION; MENKES SYNDROME; NONHUMAN; PRIORITY JOURNAL; PROTEIN CONFORMATION; PROTEIN DOMAIN; PROTEIN TRANSPORT; REGULATORY MECHANISM; TRANS GOLGI NETWORK; WILSON DISEASE;

ADENOSINE TRIPHOSPHATASES; ANIMALS; BLOTTING, WESTERN; CATALYSIS; CATION TRANSPORT PROTEINS; CHO CELLS; COPPER; CRICETINAE; FLUORESCENT ANTIBODY TECHNIQUE; GENETIC COMPLEMENTATION TEST; MUTAGENESIS; PHOSPHORYLATION; PROTEIN TRANSPORT; RECOMBINANT FUSION PROTEINS; SUBCELLULAR FRACTIONS;

ANIMALIA;

EID: 2242427117     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.M208864200     Document Type: Article

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