Structural studies of AntD: An N-acyltransferase involved in the biosynthesis of d-anthrose

Biochemistry

Volumn 51, Issue 4, 2012, Pages 867-878

  Kubiak, Rachel L ^a   Holden, Hazel M ^a  

^a UNIVERSITY OF WISCONSIN MADISON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACYL DONORS; AMINO GROUP; BACILLUS ANTHRACIS; CARBONYL OXYGEN; CATALYTIC EFFICIENCIES; CATALYTIC MECHANISMS; CONFORMATIONAL CHANGE; D-GLUCOSE; ENZYMATIC ACTIVITIES; HIGH-RESOLUTION STRUCTURES; HYDROGEN BONDINGS; INFECTIOUS AGENTS; MUTANT PROTEINS; OXYANION HOLE; SIDE-CHAINS; STRUCTURAL STUDIES; SUBSTRATE BINDING; SUBSTRATE INHIBITION; TERNARY COMPLEX; THREE-DIMENSIONAL STRUCTURE; WILD-TYPE ENZYMES;

BACILLI; BACILLUS CEREUS; BACTERIOLOGY; BIOCHEMISTRY; BIOSYNTHESIS; ENZYMES; GLUCOSE; HYDROGEN; HYDROGEN BONDS;

PROTEINS;

3 HYDROXY 3 METHYLBUTYRYL COENZYME A; ACYLTRANSFERASE; ALANINE; AMINE; AMINO ACID DERIVATIVE; ANTHROSE; ASPARAGINE; ASPARTIC ACID; BACTERIAL ENZYME; CARBONYL OXYGEN; COENZYME A; GLUCOSE DERIVATIVE; GLUTAMINE; HYDROGEN; MUTANT PROTEIN; OXYGEN DERIVATIVE; PROTEIN; SERINE; SUGAR; THYMIDINE DIPHOSPHATE; THYMIDINE DIPHOSPHATE 4 AMINO 4,6 DIDEOXYGLUCOSE; UNCLASSIFIED DRUG;

ACYLATION; AMINO ACID SUBSTITUTION; ANIMAL EXPERIMENT; ARTICLE; BACILLUS CEREUS; BACTERIAL STRAIN; CATALYSIS; COMPLEX FORMATION; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME STRUCTURE; ENZYME SUBSTRATE; ENZYME SYNTHESIS; HYDROGEN BOND; KINETICS; NONHUMAN; PRIORITY JOURNAL; PROTEIN CONFORMATION; PROTEIN QUATERNARY STRUCTURE; WILD TYPE;

ACYL COENZYME A; ACYLTRANSFERASES; AMINO ACID SUBSTITUTION; AMINO SUGARS; ASPARTIC ACID; BACILLUS CEREUS; BACTERIAL PROTEINS; BIOCATALYSIS; CATALYTIC DOMAIN; COENZYME A; CRYSTALLOGRAPHY, X-RAY; DEOXY SUGARS; DEOXYGLUCOSE; KINETICS; MODELS, MOLECULAR; MUTAGENESIS, SITE-DIRECTED; MUTANT PROTEINS; PROTEIN CONFORMATION; RECOMBINANT PROTEINS; SERINE; THYMINE NUCLEOTIDES;

BACILLUS ANTHRACIS; BACILLUS CEREUS; BACTERIA (MICROORGANISMS);

EID: 84856499397     PISSN: 00062960     EISSN: 15204995     Source Type: Journal    
DOI: 10.1021/bi201650c     Document Type: Article

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