Cyclophilin-D binds strongly to complexes of the voltage-dependent anion channel and the adenine nucleotide translocase to form the permeability transition pore

European Journal of Biochemistry

Volumn 258, Issue 2, 1998, Pages 729-735

  Crompton, Martin ^a   Virji, Sukaina ^a   Ward, John M ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

Adenine nucleotide translocase; Cyclophilin; Permeability transition pore; Porin

Indexed keywords

ADENINE NUCLEOTIDE TRANSLOCASE; ANION CHANNEL; BINDING PROTEIN; CYCLOPHILIN; GLUTATHIONE TRANSFERASE; HYBRID PROTEIN; PORIN;

AMINO TERMINAL SEQUENCE; ANIMAL CELL; ARTICLE; ENZYME ACTIVITY; ESCHERICHIA COLI; FLUOROMETRY; GENE EXPRESSION; MEMBRANE PERMEABILITY; MOLECULAR CLONING; NONHUMAN; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN BINDING; RAT; WESTERN BLOTTING;

ANIMALIA; ESCHERICHIA COLI;

EID: 0032401567     PISSN: 00142956     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1432-1327.1998.2580729.x     Document Type: Article

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