Synechocystis DrgA protein functioning as nitroreductase and ferric reductase is capable of catalyzing the Fenton reaction

FEBS Journal

Volumn 274, Issue 5, 2007, Pages 1318-1327

  Takeda, Kouji ^a   Iizuka, Mayumi ^a   Watanabe, Toshihiro ^a   Nakagawa, Junichi ^a   Kawasaki, Shinji ^a   Niimura, Youichi ^a  

^a TOKYO UNIVERSITY OF AGRICULTURE   (Japan)

Author keywords

DrgA; Fenton reaction; Flavin reductase; Iron(III) reductase; Nitroreductase

Indexed keywords

BACTERIAL PROTEIN; CHELATING AGENT; DRGA PROTEIN; EDETIC ACID; FERRIC ION; FERRITIN; FLAVIN REDUCTASE; FLAVINE ADENINE NUCLEOTIDE; IRON REDUCTASE; NITROREDUCTASE; OXIDOREDUCTASE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE (PHOSPHATE) DEHYDROGENASE (QUINONE); TERT BUTYL HYDROPEROXIDE; TRANSFERRIN; UNCLASSIFIED DRUG;

AMINO TERMINAL SEQUENCE; ARTICLE; CATALYSIS; ELECTRON; ENZYME ACTIVITY; ENZYME PURIFICATION; FENTON REACTION; MOLECULAR WEIGHT; MUTANT; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN FUNCTION; REDUCTION; SYNECHOCYSTIS;

CATALYSIS; CHELATING AGENTS; EDETIC ACID; FLAVIN MONONUCLEOTIDE; FMN REDUCTASE; IRON; KINETICS; NAD; NADP; NITROREDUCTASES; OXIDATION-REDUCTION; SUBSTRATE SPECIFICITY; SYNECHOCYSTIS; TERT-BUTYLHYDROPEROXIDE;

SYNECHOCYSTIS;

EID: 33846946121     PISSN: 1742464X     EISSN: 17424658     Source Type: Journal    
DOI: 10.1111/j.1742-4658.2007.05680.x     Document Type: Article

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