about
P185
Genomic plasticity of the causative agent of melioidosis, Burkholderia pseudomalleiThe Scottish Structural Proteomics Facility: targets, methods and outputsAcsD catalyzes enantioselective citrate desymmetrization in siderophore biosynthesisStructure and Function of the RedJ Protein, a Thioesterase from the Prodiginine Biosynthetic Pathway in Streptomyces coelicolorStructural Basis for Acyl Acceptor Specificity in the Achromobactin Biosynthetic Enzyme AcsDFunctional and Structural Analysis of the Siderophore Synthetase AsbB through Reconstitution of the Petrobactin Biosynthetic Pathway from Bacillus anthracisEngineering p-hydroxyphenylpyruvate dioxygenase to a p-hydroxymandelate synthase and evidence for the proposed benzene oxide intermediate in homogentisate formationThe insect pathogen Serratia marcescens Db10 uses a hybrid non-ribosomal peptide synthetase-polyketide synthase to produce the antibiotic althiomycinPCR-targeted Streptomyces gene replacement identifies a protein domain needed for biosynthesis of the sesquiterpene soil odor geosmin.A new family of ATP-dependent oligomerization-macrocyclization biocatalysts.The complete genome sequence and comparative genome analysis of the high pathogenicity Yersinia enterocolitica strain 8081.Purification, crystallization and data collection of Pectobacterium chrysanthemi AcsD, a type A siderophore synthetaseThe dynamic architecture of the metabolic switch in Streptomyces coelicolor.Watasemycin biosynthesis in Streptomyces venezuelae: thiazoline C-methylation by a type B radical-SAM methylase homologueIdentification of a bioactive 51-membered macrolide complex by activation of a silent polyketide synthase in Streptomyces ambofaciens.Ribosomally synthesized and post-translationally modified peptide natural products: overview and recommendations for a universal nomenclature.Genome mining of Streptomyces ambofaciens.A widely distributed bacterial pathway for siderophore biosynthesis independent of nonribosomal peptide synthetases.Antimalarial activity of natural and synthetic prodiginines.Structural aspects of non-ribosomal peptide biosynthesis.Mechanisms for incorporation of glycerol-derived precursors into polyketide metabolites.Cytochrome P450–catalyzed L-tryptophan nitration in thaxtomin phytotoxin biosynthesis.2-Alkyl-4-hydroxymethylfuran-3-carboxylic acids, antibiotic production inducers discovered by Streptomyces coelicolor genome mining.Genome mining for novel natural product discovery.Genomic and genetic analyses of diversity and plant interactions of Pseudomonas fluorescens.Recent advances in siderophore biosynthesis.A crotonyl-CoA reductase-carboxylase independent pathway for assembly of unusual alkylmalonyl-CoA polyketide synthase extender units.New natural product biosynthetic chemistry discovered by genome mining.The long-overlooked enzymology of a nonribosomal peptide synthetase-independent pathway for virulence-conferring siderophore biosynthesis.Tailoring reactions catalyzed by heme-dependent enzymes: spectroscopic characterization of the L-tryptophan-nitrating cytochrome P450 TxtE.Oxidative tailoring reactions catalyzed by nonheme iron-dependent enzymes: streptorubin B biosynthesis as an example.Exploitation of the Streptomyces coelicolor A3(2) genome sequence for discovery of new natural products and biosynthetic pathways.Discovery of microbial natural products by activation of silent biosynthetic gene clusters.Discovery and Biosynthesis of Gladiolin: A Burkholderia gladioli Antibiotic with Promising Activity against Mycobacterium tuberculosis.Structure, Chemical Synthesis, and Biosynthesis of Prodiginine Natural Products.Mechanistic insights into class B radical-S-adenosylmethionine methylases: ubiquitous tailoring enzymes in natural product biosynthesis.Discovery of Unusual Biaryl Polyketides by Activation of a Silent Streptomyces venezuelae Biosynthetic Gene Cluster.Type III polyketide synthase beta-ketoacyl-ACP starter unit and ethylmalonyl-CoA extender unit selectivity discovered by Streptomyces coelicolor genome mining.Strategies for the discovery of new natural products by genome mining.Unique post-translational oxime formation in the biosynthesis of the azolemycin complex of novel ribosomal peptides from Streptomyces sp. FXJ1.264
P50
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P50
description
organic chemist
@en
scheikundige
@nl
عالم كيمياء عضوية
@ar
name
Gregory L. Challis
@ast
Gregory L. Challis
@en
Gregory L. Challis
@es
Gregory L. Challis
@sl
غريغوري ل. تشاليس
@ar
type
label
Gregory L. Challis
@ast
Gregory L. Challis
@en
Gregory L. Challis
@es
Gregory L. Challis
@sl
غريغوري ل. تشاليس
@ar
altLabel
Greg Challis
@en
prefLabel
Gregory L. Challis
@ast
Gregory L. Challis
@en
Gregory L. Challis
@es
Gregory L. Challis
@sl
غريغوري ل. تشاليس
@ar
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0000-0001-5976-3545