[HTML][HTML] Identification of novel mycobacterium tuberculosis leucyl-tRNA synthetase inhibitor using a knowledge-based computational screening approach

FA Alsulaimany, H Almukadi, NMO Zabermawi… - Journal of King Saud …, 2022 - Elsevier
Objectives Tuberculosis is a chronic lung disease caused by Mycobacterium tuberculosis
(MTB), whose thick cell envelope and drug metabolizing enzymes offering it multidrug …

Insights into the Effects of Ligand Binding on Leucyl-tRNA Synthetase Inhibitors for Tuberculosis: In Silico Analysis and Isothermal Titration Calorimetry Validation

ZU Rehman, A Najmi, K Zoghebi - Biomolecules, 2024 - mdpi.com
Incidences of drug-resistant tuberculosis have become common and are rising at an
alarming rate. Aminoacyl t-RNA synthetase has been validated as a newer target against …

Discovery of potent anti-tuberculosis agents targeting leucyl-tRNA synthetase

OI Gudzera, AG Golub, VG Bdzhola… - Bioorganic & Medicinal …, 2016 - Elsevier
Tuberculosis is a serious infectious disease caused by human pathogen bacteria
Mycobacterium tuberculosis. Bacterial drug resistance is a very significant medical problem …

In silico based virtual screening and mixed mode QM/MM calculation identifies caffeine scaffold for designing potential inhibitors for tyrosyl tRNA synthetase of M …

R Sathya, S Thamotharan - International Journal of Quantum …, 2015 - Wiley Online Library
Aminoacyl tRNA synthetases are novel antibacterial drug target because of their important
role in protein synthesis. In this study, we performed high throughput virtual screening of …

Anti-Tuberculosis Potential of OJT008 against Active and Multi-Drug-Resistant Mycobacterium Tuberculosis: In Silico and In Vitro Inhibition of Methionine …

C Onyenaka, KA Idowu, NP Ha, EA Graviss… - International Journal of …, 2023 - mdpi.com
Despite the recent progress in the diagnosis of tuberculosis (TB), the chemotherapeutic
management of TB continues to be challenging. Mycobacterium tuberculosis (Mtb), the …

Identification of Dual-Targeted Mycobacterium Tuberculosis Aminoacyl-tRNA Synthetase Inhibitors Using Machine Learning

GP Volynets, MO Usenko, OI Gudzera… - Future Medicinal …, 2022 - Taylor & Francis
Background: The most serious challenge in the treatment of tuberculosis is the multidrug
resistance of Mycobacterium tuberculosis to existing antibiotics. As a strategy to overcome …

Identification of Trypanosoma brucei leucyl-tRNA synthetase inhibitors by pharmacophore-and docking-based virtual screening and synthesis

Y Zhao, Q Wang, Q Meng, D Ding, H Yang… - Bioorganic & medicinal …, 2012 - Elsevier
Human African trypanosomiasis (HAT), caused by the protozoan parasite Trypanosoma
brucei, is a neglected fatal disease. Leucyl-tRNA synthetase (LeuRS), which has been …

An in silico approach to identify potential inhibitors against multiple drug targets of Mycobacterium tuberculosis

S Kumar, P Sahu, L Jena - The International Journal of …, 2019 - journals.lww.com
Background: The increasing incidence of multidrug-resistant cases of tuberculosis (TB) and
difficulty in treating these cases requires an urgent need to find an effective anti-TB drug …

Screening of natural compounds that targets glutamate racemase of Mycobacterium tuberculosis reveals the anti-tubercular potential of flavonoids

A Pawar, P Jha, M Chopra, U Chaudhry, D Saluja - Scientific reports, 2020 - nature.com
Tuberculosis (TB) is caused by Mycobacterium tuberculosis (MTB), a highly infectious
disease accounting for nearly 1.5 million deaths every year and has been a major global …

Computational screening of natural MtbDXR inhibitors for novel anti-tuberculosis compound discovery

S Islam, R Salekeen, A Ashraf - Journal of Biomolecular Structure …, 2024 - Taylor & Francis
Abstract DXR (1-deoxy-d-xylulose-5-phosphate reductoisomerase) is an essential enzyme
in the Methylerythritol 4-phosphate (MEP) pathway, which is used by M. tuberculosis and a …