Functional expression of the Menkes disease protein reveals common biochemical mechanisms among the copper-transporting P-type ATPases

Journal of Biological Chemistry

Volumn 273, Issue 6, 1998, Pages 3765-3770

  Payne, Aimee S ^a   Gitlin, Jonathan D ^a,b  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b ST LOUIS CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; COMPLEMENTARY DNA; OXIDOREDUCTASE;

AMINO ACID SEQUENCE; ARTICLE; COPPER METABOLISM; MENKES SYNDROME; NONHUMAN; OPEN READING FRAME; PRIORITY JOURNAL; PROTEIN EXPRESSION; SACCHAROMYCES CEREVISIAE; SITE DIRECTED MUTAGENESIS; STRUCTURE ACTIVITY RELATION;

ADENOSINE TRIPHOSPHATASES; AMINO ACID SEQUENCE; CARRIER PROTEINS; CATION TRANSPORT PROTEINS; DNA, COMPLEMENTARY; HELA CELLS; HUMANS; MOLECULAR SEQUENCE DATA; MUTAGENESIS, SITE-DIRECTED; PROTEIN CONFORMATION; RECOMBINANT FUSION PROTEINS; SACCHAROMYCES CEREVISIAE;

EID: 0032488829     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.273.6.3765     Document Type: Article

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