An atomic-level investigation of the disease-causing A629P mutant of the menkes protein, ATP7A

Journal of Molecular Biology

Volumn 352, Issue 2, 2005, Pages 409-417

  Banci, Lucia ^a,b   Bertini, Ivano ^a   Cantini, Francesca ^a   Migliardi, Manuele ^a   Rosato, Antonio ^a   Wang, Shenlin ^a  

^a UNIVERSITY OF FLORENCE   (Italy)

^b FiorGen   (Italy)

Author keywords

ATP7A; Copper; Hydrogen exchange; Menkes disease; Metal homeostasis

Indexed keywords

ADENOSINE TRIPHOSPHATE; AMINO ACID; COPPER; MENKES PROTEIN;

AMINO ACID SUBSTITUTION; ARTICLE; BETA SHEET; GENE MUTATION; GENETIC SUSCEPTIBILITY; MENKES SYNDROME; MOLECULAR BIOLOGY; PATHOPHYSIOLOGY; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN DOMAIN; PROTEIN PROTEIN INTERACTION; PROTEIN STRUCTURE; PROTEIN TRANSPORT; RECEPTOR AFFINITY; STRUCTURE ANALYSIS;

EID: 23944471692     PISSN: 00222836     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jmb.2005.07.034     Document Type: Article

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