Theoretical insights on the binding of isoniazid to the active site residues of Mycobacterium tuberculosis catalase-peroxidase
Author:
Funder
University Research Coordination Office of De La Salle University
Publisher
Elsevier BV
Subject
Infectious Diseases,Microbiology (medical),Immunology,Microbiology
Reference42 articles.
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5. Characterization of the catalase-peroxidase gene (katG) and inhA locus in isoniazid-resistant and -susceptible strains of Mycobacterium tuberculosis by automated DNA sequencing: restricted array of mutations associated with drug resistance;Musser;J Infect Dis,1996
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1. Synthesis of isoniazid analogs with promising antituberculosis activity and bioavailability: Biological evaluation and computational studies;Journal of Molecular Structure;2023-07
2. Genotypic Characterization of katG, inhA, and ahpC in Isoniazid-Resistant Mycobacterium tuberculosis Clinical Isolates in Shanghai, China;Jundishapur Journal of Microbiology;2020-01-15
3. Applications of Molecular Simulation in the Discovery of Antituberculosis Drugs: A Review;Protein & Peptide Letters;2019-09-16
4. DFT study on the effect of proximal residues on the Mycobacterium tuberculosis catalase-peroxidase (katG) heme compound I intermediate and its bonding interaction with isoniazid;Physical Chemistry Chemical Physics;2019
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