2.37A structure of gepotidacin with S.aureus DNA gyrase and uncleaved DNA

NIAID Data Ecosystem2026-05-02 收录

抗生素-靶点复合物结构

抗菌药物机制

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2.37A structure of gepotidacin with S.aureus DNA gyrase and uncleaved DNA

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2024-05-15

Transcriptome response of Pseudomonas aeruginosa PA14 to antimicrobial peptides

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We analyzed the transcriptome of P. aeruginosa grown for 16h in the presence or absence of 0.25 x MIC of polymyxinB, G3KL or T7 Comparative transcriptome in triplicate samples

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Subinhibitory concentrations of compound used to assess their influence on the gene expression profile of Bacillus anthracis. Bacillus anthracis cells were treated with 0.25X MIC of compound (Me2-Arg-

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A. baumannii MsbA in complex with TBT1 decoupler

细菌蛋白结构

抗菌药物机制

A. baumannii MsbA in complex with TBT1 decoupler Descriptor: 2-(4-chlorobenzamido)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylic acid, ATP-dependent lipid A-core flippase Authors: Thelot, F, Liao,

Protein Data Bank Japan2024-05-29 更新60

The Proteomic Response of Mycobacterium smegmatis to Anti-Tuberculosis Drugs Suggests Targeted Pathways

抗菌药物机制

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Mycobacterium smegmatis is a fast-growing model mycobacterial system that shares many features with the pathogenic Mycobacterium tuberculosis while allowing practical proteomics analysis. With the use

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抗菌药物机制

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We report differential regulated genes in three pathogenic bacterial strains after treatment with a new antimicrobial. Bacteria were grown in triplicates to mid-log phase in the presence or anbsence o

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2.37A structure of gepotidacin with S.aureus DNA gyrase and uncleaved DNA

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