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Volumn 278, Issue 15, 2003, Pages 13302-13308
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The role of the invariant His-1069 in folding and function of the Wilson's disease protein, the human copper-transporting ATPase ATP7B
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Author keywords
[No Author keywords available]
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Indexed keywords
CATALYSIS;
COPPER;
HYDROLYSIS;
NEUROLOGY;
HUMAN CELLS;
PROTEINS;
ADENOSINE TRIPHOSPHATASE;
ADENYLYLIMIDODIPHOSPHATE;
ALANINE;
COPPER;
CYSTEINE;
GLUTAMINE;
HISTIDINE;
MUTANT PROTEIN;
UNCLASSIFIED DRUG;
WILSON DISEASE PROTEIN;
ADENOSINE TRIPHOSPHATE;
CATION TRANSPORT PROTEIN;
PRIMER DNA;
RECOMBINANT PROTEIN;
AMINO ACID SUBSTITUTION;
ANIMAL CELL;
ARTICLE;
ATP7B GENE;
BINDING AFFINITY;
CONFORMATIONAL TRANSITION;
CONTROLLED STUDY;
ENZYME ACTIVE SITE;
GENE;
GENE MUTATION;
LIVER DISEASE;
NEUROLOGIC DISEASE;
NONHUMAN;
NUCLEOTIDE SEQUENCE;
PRIORITY JOURNAL;
PROTEIN ANALYSIS;
PROTEIN BINDING;
PROTEIN DOMAIN;
PROTEIN FOLDING;
PROTEIN LOCALIZATION;
PROTEIN PHOSPHORYLATION;
PROTEIN STRUCTURE;
STRUCTURE ANALYSIS;
WILD TYPE;
WILSON DISEASE;
AMINO ACID SEQUENCE;
BINDING SITE;
CELL MEMBRANE;
CHEMICAL STRUCTURE;
CHEMISTRY;
ENZYMOLOGY;
GENETICS;
HUMAN;
METABOLISM;
MOLECULAR GENETICS;
PROTEIN SECONDARY STRUCTURE;
SEQUENCE ALIGNMENT;
SEQUENCE HOMOLOGY;
SITE DIRECTED MUTAGENESIS;
ULTRASTRUCTURE;
ANIMALIA;
MAMMALIA;
ADENOSINE TRIPHOSPHATASES;
ADENOSINE TRIPHOSPHATE;
AMINO ACID SEQUENCE;
AMINO ACID SUBSTITUTION;
BASE SEQUENCE;
BINDING SITES;
CATION TRANSPORT PROTEINS;
CELL MEMBRANE;
DNA PRIMERS;
HEPATOLENTICULAR DEGENERATION;
HISTIDINE;
HUMANS;
MODELS, MOLECULAR;
MOLECULAR SEQUENCE DATA;
MUTAGENESIS, SITE-DIRECTED;
PROTEIN FOLDING;
PROTEIN STRUCTURE, SECONDARY;
RECOMBINANT PROTEINS;
SEQUENCE ALIGNMENT;
SEQUENCE HOMOLOGY, AMINO ACID;
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EID: 0038482198
PISSN: 00219258
EISSN: None
Source Type: Journal
DOI: 10.1074/jbc.M300034200 Document Type: Article |
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Times cited : (71)
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References (23)
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