Structure-Guided Discovery of Phenyl-diketo Acids as Potent Inhibitors of M. tuberculosis Malate Synthase
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CLYBL is a polymorphic human enzyme with malate synthase and β-methylmalate synthase activityThe application of tetracyclineregulated gene expression systems in the validation of novel drug targets in Mycobacterium tuberculosisTuberculosis drug discovery in the post-post-genomic eraMycobacterium tuberculosis Malate Synthase Structures with Fragments Reveal a Portal for Substrate/Product ExchangeA new drug for an old bugDiarylcoumarins inhibit mycolic acid biosynthesis and kill Mycobacterium tuberculosis by targeting FadD32A Hidden Markov Model for identifying essential and growth-defect regions in bacterial genomes from transposon insertion sequencing data.The phosphatidyl-myo-inositol mannosyltransferase PimA is essential for Mycobacterium tuberculosis growth in vitro and in vivoBayesian analysis of gene essentiality based on sequencing of transposon insertion libraries.Discovery of Mycobacterium tuberculosis α-1,4-glucan branching enzyme (GlgB) inhibitors by structure- and ligand-based virtual screening.The tuberculosis drug discovery and development pipeline and emerging drug targets.Therapeutic Potential of the Mycobacterium tuberculosis Mycolic Acid Transporter, MmpL3Validation of CoaBC as a Bactericidal Target in the Coenzyme A Pathway of Mycobacterium tuberculosis.Tuberculosis drug discovery and emerging targets.Identification of spirocyclic or phosphate substituted quinolizine derivatives as novel HIV-1 integrase inhibitors: a patent evaluation of WO2016094197A1, WO2016094198A1 and WO2016154527A1.Glyoxylate detoxification is an essential function of malate synthase required for carbon assimilation in Mycobacterium tuberculosis.The Mycobacterium tuberculosis H37Ra gene MRA_1916 causes growth defects upon down-regulation.Sun sets on protein initiative, casting shadow over drug discovery.Novel Pyrimidines as Antitubercular Agents.Anion-π interactions in complexes of proteins and halogen-containing amino acids.Two isocitrate dehydrogenases from a plant pathogen Xanthomonas campestris pv. campestris 8004. Bioinformatic analysis, enzymatic characterization, and implication in virulence.TnSeq of Mycobacterium tuberculosis clinical isolates reveals strain-specific antibiotic liabilities.Experimental investigation of anion-π interactions--applications and biochemical relevance.RosettaLigandEnsemble: A Small-Molecule Ensemble-Driven Docking Approach.Molecular Targets Related Drug Resistance Mechanisms in MDR-, XDR-, and TDR-Mycobacterium tuberculosis Strains.On the non-classical contribution in lone-pair–π interaction: IQA perspective
P2860
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P2860
Structure-Guided Discovery of Phenyl-diketo Acids as Potent Inhibitors of M. tuberculosis Malate Synthase
description
2012 nî lūn-bûn
@nan
2012 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Structure-Guided Discovery of ...... . tuberculosis Malate Synthase
@ast
Structure-Guided Discovery of ...... . tuberculosis Malate Synthase
@en
Structure-Guided Discovery of ...... . tuberculosis Malate Synthase
@nl
type
label
Structure-Guided Discovery of ...... . tuberculosis Malate Synthase
@ast
Structure-Guided Discovery of ...... . tuberculosis Malate Synthase
@en
Structure-Guided Discovery of ...... . tuberculosis Malate Synthase
@nl
prefLabel
Structure-Guided Discovery of ...... . tuberculosis Malate Synthase
@ast
Structure-Guided Discovery of ...... . tuberculosis Malate Synthase
@en
Structure-Guided Discovery of ...... . tuberculosis Malate Synthase
@nl
P2093
P2860
P921
P3181
P1476
Structure-Guided Discovery of ...... . tuberculosis Malate Synthase
@en
P2093
Inna V Krieger
James C Sacchettini
Joel S Freundlich
Jose-Luis Lavandera
Joshua L Owen
Justin P Roberts
Maria T Fraile
Qingan Sun
Sofia I Huss
Thomas R Ioerger
P2860
P304
P3181
P356
10.1016/J.CHEMBIOL.2012.09.018
P577
2012-12-21T00:00:00Z