LmbE proteins from Bacillus cereus are de-N-acetylases with broad substrate specificity and are highly similar to proteins in Bacillus anthracis

FEBS Journal

Volumn 277, Issue 13, 2010, Pages 2740-2753

  Deli, Alexandra ^a   Koutsioulis, Dimitrios ^b   Fadouloglou, Vasiliki E ^b   Spiliotopoulou, Panagiota ^a   Balomenou, Stavroula ^a   Arnaouteli, Sofia ^a   Tzanodaskalaki, Maria ^b   Mavromatis, Konstantinos ^c   Kokkinidis, Michalis ^a,b   Bouriotis, Vassilis ^a,b  

^a UNIVERSITY OF CRETE   (Greece)

^b INSTITUTE OF MOLECULAR BIOLOGY AND BIOTECHNOLOGY   (Greece)

^c DOE JOINT GENOME INSTITUTE   (United States)

Author keywords

Bacillus anthracis; De N acetylase; Glucosamine; LmbE; Mutational analysis

Indexed keywords

CHITIN; N ACETYL DEXTRO GLUCOSAMINE 1 PHOSPHATE; N ACETYL DEXTRO GLUCOSAMINE 6 PHOSPHATE; N ACETYL DEXTRO GLUCOSAMINYL [BETA 1,4] N ACETYLMURAMYL LEVO ALANYL DEXTRO ISOGLUTAMINE; N ACETYL DEXTRO MANNOSAMINE; N ACETYLGALACTOSAMINE; N ACETYLGLUCOSAMINE; N,N' DIACETYLCHITOBIOSE; PEPTIDOGLYCAN; PROTEIN; PROTEIN BC 1534; PROTEIN BC 3461; PROTEIN LMBE; RECOMBINANT ENZYME; UNCLASSIFIED DRUG; URIDINE 5' DIPHOSPHATE N ACETYL DEXTRO GLUCOSAMINE;

ARTICLE; BACILLUS ANTHRACIS; BACILLUS CEREUS; CATALYSIS; CRYSTAL STRUCTURE; ENZYME ACTIVITY; ENZYME KINETICS; ENZYME SPECIFICITY; ENZYME STRUCTURE; ENZYME SUBSTRATE; ESCHERICHIA COLI; GENE EXPRESSION; MOLECULAR CLONING; MOLECULAR WEIGHT; MUTATIONAL ANALYSIS; NONHUMAN; NUCLEOTIDE SEQUENCE; PH; PRIORITY JOURNAL;

AMIDOHYDROLASES; AMINO ACID SEQUENCE; BACILLUS ANTHRACIS; BACILLUS CEREUS; BACTERIAL PROTEINS; CLONING, MOLECULAR; DNA MUTATIONAL ANALYSIS; ENZYME ACTIVATION; HYDROGEN-ION CONCENTRATION; KINETICS; MODELS, MOLECULAR; MOLECULAR CONFORMATION; MOLECULAR SEQUENCE DATA; RECOMBINANT PROTEINS; SEQUENCE ALIGNMENT; SEQUENCE HOMOLOGY, AMINO ACID; SUBSTRATE SPECIFICITY; TEMPERATURE;

BACILLUS ANTHRACIS; BACILLUS CEREUS; ESCHERICHIA COLI;

EID: 77953563381     PISSN: 1742464X     EISSN: 17424658     Source Type: Journal    
DOI: 10.1111/j.1742-4658.2010.07691.x     Document Type: Article

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