Prospects for aminoacyl-tRNA synthetase inhibitors as new antimicrobial agents.
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Biotin Protein Ligase Is a Target for New AntibacterialsRecent advances in the biology and drug targeting of malaria parasite aminoacyl-tRNA synthetasesEvolutionary Limitation and Opportunities for Developing tRNA Synthetase Inhibitors with 5-Binding-Mode ClassificationtRNAs as antibiotic targetsIn silico discovery of aminoacyl-tRNA synthetase inhibitorsAsparagine requirement in Plasmodium berghei as a target to prevent malaria transmission and liver infections.Crystal structure of the aspartyl-tRNA synthetase from Entamoeba histolyticaCrystal Structures of Trypanosomal Histidyl-tRNA Synthetase Illuminate Differences between Eukaryotic and Prokaryotic HomologsFlexibility and communication within the structure of the Mycobacterium smegmatis methionyl-tRNA synthetaseThe Double-Length Tyrosyl-tRNA Synthetase from the Eukaryote Leishmania major Forms an Intrinsically Asymmetric Pseudo-DimerStructural Basis for Microcin C7 Inactivation by the MccE AcetyltransferaseStructure of the prolyl-tRNA synthetase from the eukaryotic pathogenGiardia lambliaDiscovery of a Novel Class of Boron-Based Antibacterials with Activity against Gram-Negative BacteriaBisubstrate Adenylation Inhibitors of Biotin Protein Ligase from Mycobacterium tuberculosisSelective inhibition of Biotin Protein Ligase from Staphylococcus aureusDiscovery of a potent benzoxaborole-based anti-pneumococcal agent targeting leucyl-tRNA synthetaseStructural analysis of malaria-parasite lysyl-tRNA synthetase provides a platform for drug developmentAnalogs of natural aminoacyl-tRNA synthetase inhibitors clear malaria in vivoComparative genomics analysis of Mycobacterium ulcerans for the identification of putative essential genes and therapeutic candidatesNovel hybrid virtual screening protocol based on molecular docking and structure-based pharmacophore for discovery of methionyl-tRNA synthetase inhibitors as antibacterial agentsLigand co-crystallization of aminoacyl-tRNA synthetases from infectious disease organismsLoss of cysteinyl-tRNA synthetase (CARS) induces the transsulfuration pathway and inhibits ferroptosis induced by cystine deprivationSelective and specific inhibition of the plasmodium falciparum lysyl-tRNA synthetase by the fungal secondary metabolite cladosporinUnusual domain architecture of aminoacyl tRNA synthetases and their paralogs from Leishmania majorGenome-wide Analysis of Mycoplasma hominis for the Identification of Putative Therapeutic Targets.High-resolution transcriptomic analysis of the adaptive response of Staphylococcus aureus during acute and chronic phases of osteomyelitis.Bacterial resistance to leucyl-tRNA synthetase inhibitor GSK2251052 develops during treatment of complicated urinary tract infections.Susceptibility and mode of binding of the Mycobacterium tuberculosis cysteinyl transferase mycothiol ligase to tRNA synthetase inhibitors.Identification of potent inhibitors of the Trypanosoma brucei methionyl-tRNA synthetase via high-throughput orthogonal screening.Novel and unique domains in aminoacyl-tRNA synthetases from human fungal pathogens Aspergillus niger, Candida albicans and Cryptococcus neoformans.Encyclopedia of bacterial gene circuits whose presence or absence correlate with pathogenicity--a large-scale system analysis of decoded bacterial genomesStructural Basis for Specific Inhibition of tRNA Synthetase by an ATP Competitive Inhibitor.A human leucyl-tRNA synthetase as an anticancer targetStable analogues of OSB-AMP: potent inhibitors of MenE, the o-succinylbenzoate-CoA synthetase from bacterial menaquinone biosynthesisNon-nucleoside inhibitors of BasE, an adenylating enzyme in the siderophore biosynthetic pathway of the opportunistic pathogen Acinetobacter baumannii.Aminoacyl-tRNA synthetases: essential and still promising targets for new anti-infective agents.Insights into the preclinical treatment of blood-stage malaria by the antibiotic borrelidin.Identifying the targets of aminoacyl-tRNA synthetase inhibitors by primer extension inhibition.Advances in Drug Discovery and Development for Pediatric Tuberculosis.Adenylating enzymes in Mycobacterium tuberculosis as drug targets.
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P2860
Prospects for aminoacyl-tRNA synthetase inhibitors as new antimicrobial agents.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh
2005年學術文章
@zh-hant
name
Prospects for aminoacyl-tRNA synthetase inhibitors as new antimicrobial agents.
@ast
Prospects for aminoacyl-tRNA synthetase inhibitors as new antimicrobial agents.
@en
type
label
Prospects for aminoacyl-tRNA synthetase inhibitors as new antimicrobial agents.
@ast
Prospects for aminoacyl-tRNA synthetase inhibitors as new antimicrobial agents.
@en
prefLabel
Prospects for aminoacyl-tRNA synthetase inhibitors as new antimicrobial agents.
@ast
Prospects for aminoacyl-tRNA synthetase inhibitors as new antimicrobial agents.
@en
P2093
P2860
P1476
Prospects for aminoacyl-tRNA synthetase inhibitors as new antimicrobial agents.
@en
P2093
Alexander John O'Neill
Ian Chopra
Julian Gregston Hurdle
P2860
P304
P356
10.1128/AAC.49.12.4821-4833.2005
P407
P577
2005-12-01T00:00:00Z