Evolution study of the Baeyer-Villiger monooxygenases enzyme family: Functional importance of the highly conserved residues

Biochimie

Volumn 95, Issue 7, 2013, Pages 1394-1402

  Rebehmed, Joseph ^a,b,c,d   Alphand, Véronique ^e   De Berardinis, Véronique ^f   De Brevern, Alexandre G ^a,b,c,d  

^a INSERM   (France)

^b Institut National de la Transfusion Sanguine   (France)

^c INSTITUT NATIONAL DE LA TRANSFUSION SANGUINE   (France)

^d Laboratoire d'Excellence   (France)

^e AIX MARSEILLE UNIVERSITÉ   (France)

^f DIF   (France)

Author keywords

Function; Interactions; Phylogeny; Protein structure; Sequence alignment

Indexed keywords

AMINO ACID; BAEYER VILLIGER MONOOXYGENASE; FLAVINE ADENINE NUCLEOTIDE; KETONE; OXYGEN; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE; THREONINE; UNCLASSIFIED DRUG; UNSPECIFIC MONOOXYGENASE;

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ARTICLE; BAEYER VILLIGER REACTION; BINDING SITE; DATA BASE; ENANTIOSELECTIVITY; ENZYME BINDING; ENZYME MECHANISM; ENZYME STRUCTURE; GENETIC CONSERVATION; GREEN CHEMISTRY; PHYLOGENETIC TREE; PROTEIN FAMILY; PROTEIN FUNCTION; PROTEIN INTERACTION; PROTEIN MOTIF; SEQUENCE ALIGNMENT; SEQUENCE HOMOLOGY;

BINDING SITES; CONSERVED SEQUENCE; FLAVIN-ADENINE DINUCLEOTIDE; MIXED FUNCTION OXYGENASES; NADP; PHYLOGENY; PSEUDOMONAS; RHODOCOCCUS; THREONINE;

EID: 84878596405     PISSN: 03009084     EISSN: 61831638     Source Type: Journal    
DOI: 10.1016/j.biochi.2013.03.005     Document Type: Article

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