Atox1 contains positive residues that mediate membrane association and aid subsequent copper loading

Journal of Membrane Biology

Volumn 246, Issue 12, 2013, Pages 903-913

  Flores, Adrian G ^a   Unger, Vinzenz M ^a  

^a NORTHWESTERN UNIVERSITY   (United States)

Author keywords

Atox1; Chaperone; Copper homeostasis; Copper trafficking; Membrane scaffold

Indexed keywords

COPPER; COPPER ZINC SUPEROXIDE DISMUTASE; CYSTEINE; LIPOSOME; LYSINE; PEROXIREDOXIN 3;

ARTICLE; BILAYER MEMBRANE; CONTROLLED STUDY; ENZYME LINKED IMMUNOSORBENT ASSAY; GEL PERMEATION CHROMATOGRAPHY; HUMAN; HUMAN CELL; HUMAN CELL CULTURE; IN VIVO STUDY; MASS SPECTROMETRY; MEMBRANE BINDING; MEMBRANE BIOLOGY; MUTAGENESIS; MUTATION; NONHUMAN; PROTEIN EXPRESSION; PROTEIN PURIFICATION; SECRETORY PATHWAY;

AMINO ACID SUBSTITUTION; AMINO ACIDS; CELL MEMBRANE; COPPER; HUMANS; METALLOCHAPERONES; MODELS, MOLECULAR; MUTATION; PROTEIN BINDING; PROTEIN CONFORMATION;

EID: 84888301851     PISSN: 00222631     EISSN: 14321424     Source Type: Journal    
DOI: 10.1007/s00232-013-9592-1     Document Type: Article

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