Structural characterization of AtmS13, a putative sugar aminotransferase involved in indolocarbazole AT2433 aminopentose biosynthesis

Proteins: Structure, Function and Bioinformatics

Volumn 83, Issue 8, 2015, Pages 1547-1554

  Singh, Shanteri ^a   Kim, Youngchang ^b   Wang, Fengbin ^c   Bigelow, Lance ^b   Endres, Michael ^b   Kharel, Madan K ^d   Babnigg, Gyorgy ^b   Bingman, Craig A ^e   Joachimiak, Andrzej ^b   Thorson, Jon S ^a   Phillips, George N ^c,e  

^a UNIVERSITY OF KENTUCKY   (United States)

^b ARGONNE NATIONAL LABORATORY   (United States)

^c RICE UNIVERSITY   (United States)

^d UNIVERSITY OF MARYLAND EASTERN SHORE   (United States)

^e UNIVERSITY OF WISCONSIN MADISON   (United States)

Author keywords

Carbohydrate; Indolocarbazole; Natural product; Sugar nucleotide; Transamination; X ray crystallography

Indexed keywords

AMINOTRANSFERASE S13; ANTINEOPLASTIC ANTIBIOTIC; ASPARTATE AMINOTRANSFERASE; ASPARTATE AMINOTRANSFERASE FOLD TYPE 1; AT 2433; AT2433; ATMS13 PROTEIN; BACTERIAL ENZYME; CALICHEAMICIN DERIVATIVE; CALLOSE SYNTHASE 13; CALS13 PROTEIN; CARBAZOLE DERIVATIVE; CARBOXYLIC ACID; HEXOSE; HOMODIMER; HYDROXYL GROUP; INDOLE DERIVATIVE; LYSINE; MONOMER; PENTOSE; PYRIDINIUM DERIVATIVE; PYRIDOXAL 5 PHOSPHATE; SELENOMETHIONINE; SUGAR NUCLEOTIDE; UNCLASSIFIED DRUG; AMINOTRANSFERASE; BACTERIAL PROTEIN; RECOMBINANT PROTEIN;

ACTINOMADURA MELLIAURA; ARTICLE; BETA SHEET; BINDING SITE; BIOSYNTHESIS; CONTROLLED STUDY; CRYSTAL STRUCTURE; DRUG SYNTHESIS; ENZYME ACTIVE SITE; ENZYME ACTIVITY; ENZYME ANALYSIS; ENZYME SPECIFICITY; ENZYME STRUCTURE; GENOMICS; HYDROGEN BOND; MOLECULAR INTERACTION; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN FOLDING; PROTEIN STRUCTURE; PROTON TRANSPORT; SURFACE AREA; TRANSAMINATION; X RAY CRYSTALLOGRAPHY; ACTINOMYCETALES; CHEMISTRY; ENZYMOLOGY; GENETICS; METABOLISM; MOLECULAR MODEL;

ACTINOMADURA;

ACTINOMYCETALES; BACTERIAL PROTEINS; BINDING SITES; CARBAZOLES; CRYSTALLOGRAPHY, X-RAY; MODELS, MOLECULAR; RECOMBINANT PROTEINS; TRANSAMINASES;

EID: 84937739542     PISSN: 08873585     EISSN: 10970134     Source Type: Journal    
DOI: 10.1002/prot.24844     Document Type: Article

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