In vitro-mutagenesis of NADPH:protochlorophyllide oxidoreductase B: Two distinctive protochlorophyllide binding sites participate in enzyme catalysis and assembly

Molecular Genetics and Genomics

Volumn 275, Issue 6, 2006, Pages 540-552

  Reinbothe, Christiane ^a   Buhr, Frank ^a   Bartsch, Sandra ^a   Desvignes, Claire ^b   Quigley, Françoise ^b   Pesey, Hélène ^b   Reinbothe, Steffen ^b  

^a UNIVERSITY OF BAYREUTH   (Germany)

^b CNRS   (France)

Author keywords

(POR) B; Chlorophyll biosynthesis; Homology modelling; In vitro mutagenesis; LHPP; NADPH:protochlorophyllide oxidoreductase

Indexed keywords

CYSTEINE; OXIDOREDUCTASE; PIGMENT; PROTOCHLOROPHYLLIDE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE;

ANGIOSPERM; ARTICLE; BINDING AFFINITY; BINDING SITE; BIOCHEMISTRY; CATALYSIS; ENZYME MECHANISM; EVOLUTION; MUTAGENESIS; NONHUMAN; PLANT; PLASTID; PRIORITY JOURNAL;

AMINO ACID SEQUENCE; BASE SEQUENCE; CATALYSIS; DNA PRIMERS; MOLECULAR SEQUENCE DATA; MUTAGENESIS; OXIDOREDUCTASES ACTING ON CH-CH GROUP DONORS; SEQUENCE HOMOLOGY, AMINO ACID;

MAGNOLIOPHYTA;

EID: 33746076676     PISSN: 16174615     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00438-006-0109-9     Document Type: Article

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