A structural model of the copper ATPase ATP7B to facilitate analysis of Wilson disease-causing mutations and studies of the transport mechanism

Metallomics

Volumn 4, Issue 7, 2012, Pages 669-678

  Schushan, Maya ^a   Bhattacharjee, Ashima ^b   Ben Tal, Nir ^a   Lutsenko, Svetlana ^b  

^a TEL AVIV UNIVERSITY   (Israel)

^b JOHNS HOPKINS UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MODEL STRUCTURES; NEURODEGENERATIVE DISEASES;

BRAIN FUNCTIONS; DELETERIOUS EFFECTS; EVOLUTIONARY CONSERVATIONS; HUMAN PHYSIOLOGY; LOW FREQUENCY; MOLECULAR INTERPRETATION; STRUCTURAL FEATURE; STRUCTURAL MODELS; TRANSPORT MECHANISM; WILSON DISEASE;

COPPER;

WILSON DISEASE PROTEIN;

CONFERENCE PAPER; GENOTYPE; HUMAN; HYDROPHOBICITY; MISSENSE MUTATION; MOLECULAR MECHANICS; MUTAGENESIS; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN BINDING; WILSON DISEASE;

BACTERIA (MICROORGANISMS); EUKARYOTA;

EID: 84863708072     PISSN: 17565901     EISSN: 1756591X     Source Type: Journal    
DOI: 10.1039/c2mt20025b     Document Type: Conference Paper

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