Residue Leu940 has a crucial role in the linkage and reaction specificity of the glucansucrase GTF180 of the probiotic bacterium lactobacillus reuteri 180

Journal of Biological Chemistry

Volumn 289, Issue 47, 2014, Pages 32773-32782

  Meng, Xiangfeng ^a   Dobruchowska, Justyna M ^a   Pijning, Tjaard ^a   López, Cesar A ^a,b   Kamerling, Johannis P ^a   Dijkhuizen, Lubbert ^a  

^a UNIVERSITY OF GRONINGEN   (Netherlands)

^b LOS ALAMOS NATIONAL LABORATORY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; AROMATIC COMPOUNDS; BACTERIA; GLUCOSE; HYDROLASES; MALTOSE; OLIGOSACCHARIDES; POLYSACCHARIDES; SUGAR (SUCROSE); SYNTHESIS (CHEMICAL);

DIFFERENT STRUCTURE; GLYCOSIDE HYDROLASES; ISOMALTO-OLIGOSACCHARIDES; LACTOBACILLUS REUTERI; OLIGOSACCHARIDE SYNTHESIS; PHYSICOCHEMICAL PROPERTY; STRUCTURAL DETERMINANTS; STRUCTURE-FUNCTION RELATIONSHIP;

CRYSTAL STRUCTURE;

BACTERIAL ENZYME; GLUCANSUCRASE GTF180; GLYCOSIDASE; LEUCINE; OLIGOSACCHARIDE; POLYSACCHARIDE; PROBIOTIC AGENT; TRYPTOPHAN; UNCLASSIFIED DRUG; ALTERNANSUCRASE; BACTERIAL PROTEIN; GLUCAN; GLUCOSE; GLYCOSYLTRANSFERASE; MALTOSE; PROTEIN BINDING; SUCROSE;

ANION EXCHANGE CHROMATOGRAPHY; ARTICLE; BINDING KINETICS; BINDING SITE; CARBOHYDRATE SYNTHESIS; ENZYME ACTIVITY; ENZYME ASSAY; ENZYME SPECIFICITY; ENZYME STRUCTURE; LACTOBACILLUS REUTERI; MOLECULAR DOCKING; MUTATION; NONHUMAN; NUCLEOTIDE SEQUENCE; PHYSICAL CHEMISTRY; PROTEIN DOMAIN; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ACTIVITY RELATION; WILD TYPE; CHEMISTRY; CONFORMATION; ENZYMOLOGY; GENETICS; METABOLISM; PROTEIN TERTIARY STRUCTURE; X RAY CRYSTALLOGRAPHY;

BACTERIA (MICROORGANISMS); LACTOBACILLUS REUTERI;

BACTERIAL PROTEINS; CARBOHYDRATE CONFORMATION; CRYSTALLOGRAPHY, X-RAY; GLUCANS; GLUCOSE; GLYCOSYLTRANSFERASES; LACTOBACILLUS REUTERI; LEUCINE; MALTOSE; MOLECULAR DOCKING SIMULATION; MUTATION; OLIGOSACCHARIDES; PROBIOTICS; PROTEIN BINDING; PROTEIN STRUCTURE, TERTIARY; SUBSTRATE SPECIFICITY; SUCROSE; TRYPTOPHAN;

EID: 84911887172     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M114.602524     Document Type: Article

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