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Exploiting the reversibility of natural product glycosyltransferase-catalyzed reactions

Exploiting the reversibility of natural product glycosyltransferase-catalyzed reactions

http://www.wikidata.org/entity/Q28261250

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Characterization of glycosyltransferase DesVII and its auxiliary partner protein DesVIII in the methymycin/picromycin biosynthetic pathway Natural product disaccharide engineering through tandem glycosyltransferase catalysis reversibility and neoglycosylation Biochemical and structural insights of the early glycosylation steps in calicheamicin biosynthesis Complete set of glycosyltransferase structures in the calicheamicin biosynthetic pathway reveals the origin of regiospecificity Accessing Nature's diversity through metabolic engineering and synthetic biology Structural characterization of CalO2: A putative orsellinic acid P450 oxidase in the calicheamicin biosynthetic pathway Directed Evolution and Structural Characterization of a Simvastatin Synthase Expanding the Nucleotide and Sugar 1-Phosphate Promiscuity of Nucleotidyltransferase RmlA via Directed Evolution Structural characterization of CalO1: a putative orsellinic acid methyltransferase in the calicheamicin-biosynthetic pathway Structure of a Dinuclear Iron Cluster-Containing β-Hydroxylase Active in Antibiotic Biosynthesis Structural Studies of the Spinosyn Forosaminyltransferase, SpnP Structure-Guided Functional Characterization of Enediyne Self-Sacrifice Resistance Proteins, CalU16 and CalU19 Using simple donors to drive the equilibria of glycosyltransferase-catalyzed reactions Enzymatic methods for glyco(diversification/randomization) of drugs and small molecules The in vitro characterization of polyene glycosyltransferases AmphDI and NysDI Natural-product sugar biosynthesis and enzymatic glycodiversification.Trans-sialidase activity of Photobacterium damsela alpha2,6-sialyltransferase and its application in the synthesis of sialosides Optimizing glycosyltransferase specificity via "hot spot" saturation mutagenesis presents a catalyst for novobiocin glycorandomization.A simple strategy for glycosyltransferase-catalyzed aminosugar nucleotide synthesis.A general NMR-based strategy for the in situ characterization of sugar-nucleotide-dependent biosynthetic pathways.Characterization of the calicheamicin orsellinate C2-O-methyltransferase CalO6.Natural products version 2.0: connecting genes to molecules.Functionalized anodic aluminum oxide membrane-electrode system for enzyme immobilization.Recombinant E. coli prototype strains for in vivo glycorandomization.Probing the aglycon promiscuity of an engineered glycosyltransferase Terfestatins B and C, New p-Terphenyl Glycosides Produced by Streptomyces sp. RM-5-8 Identification of Neuroprotective Spoxazomicin and Oxachelin Glycosides via Chemoenzymatic Glycosyl-Scanning.The impact of enzyme engineering upon natural product glycodiversification Preliminary X-ray crystallographic analysis of the glycosyltransferase from a marine Streptomyces species.Glycosyloxyamine neoglycosylation: a model study using calicheamicin.Engineering a Carbohydrate-processing Transglycosidase into Glycosyltransferase for Natural Product Glycodiversification.A comprehensive review of glycosylated bacterial natural products.Characterization of Early Enzymes Involved in TDP-Aminodideoxypentose Biosynthesis en Route to Indolocarbazole AT2433.Structural Characterization of CalS8, a TDP-α-D-Glucose Dehydrogenase Involved in Calicheamicin Aminodideoxypentose Biosynthesis Loop dynamics of thymidine diphosphate-rhamnose 3'-O-methyltransferase (CalS11), an enzyme in calicheamicin biosynthesis.Broadening the scope of glycosyltransferase-catalyzed sugar nucleotide synthesis Increasing carbohydrate diversity via amine oxidation: aminosugar, hydroxyaminosugar, nitrososugar, and nitrosugar biosynthesis in bacteria Structural dynamics of a methionine γ-lyase for calicheamicin biosynthesis: Rotation of the conserved tyrosine stacking with pyridoxal phosphate.Realizing the Promise of Chemical Glycobiology.Functional characterization and substrate specificity of spinosyn rhamnosyltransferase by in vitro reconstitution of spinosyn biosynthetic enzymes

P2860

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P2860

Exploiting the reversibility of natural product glycosyltransferase-catalyzed reactions

http://www.wikidata.org/entity/Q28261250

description

2006 nî lūn-bûn

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2006 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2006 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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name

Exploiting the reversibility of natural product glycosyltransferase-catalyzed reactions

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Exploiting the reversibility of natural product glycosyltransferase-catalyzed reactions

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Exploiting the reversibility of natural product glycosyltransferase-catalyzed reactions

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Exploiting the reversibility of natural product glycosyltransferase-catalyzed reactions

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Exploiting the reversibility of natural product glycosyltransferase-catalyzed reactions

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Exploiting the reversibility of natural product glycosyltransferase-catalyzed reactions

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Exploiting the reversibility of natural product glycosyltransferase-catalyzed reactions

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Exploiting the reversibility of natural product glycosyltransferase-catalyzed reactions

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Exploiting the reversibility of natural product glycosyltransferase-catalyzed reactions

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Exploiting the reversibility of natural product glycosyltransferase-catalyzed reactions

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Byron R Griffith

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Christoph Albermann

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In-Kyoung Lee

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Lingjun Li

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Qiang Fu

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Xun Fu

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1980893

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313

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Changsheng Zhang

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2006-09-01T00:00:00Z

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6842988

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