Elucidating the function of hypothetical PE_PGRS45 protein of Mycobacterium tuberculosis as an oxido-reductase: a potential target for drug repurposing for the treatment of tuberculosis
Author:
Affiliation:
1. DSKC Bio Discovery Lab and Department of Zoology, Miranda House, University of Delhi, New Delhi, India
2. Laboratory of Molecular Biology and Genetic Engineering, School of Biotechnology, Jawaharlal Nehru University, New Delhi, India
Funder
Department of Science and Technology (DST), Government of India
Publisher
Informa UK Limited
Link
https://www.tandfonline.com/doi/pdf/10.1080/07391102.2022.2151514
Reference61 articles.
1. Triacylglycerol and wax ester-accumulating machinery in prokaryotes
2. The Mycobacterium tuberculosis Very-Long-Chain Fatty Acyl-CoA Synthetase: Structural Basis for Housing Lipid Substrates Longer than the Enzyme
3. New insights into the mycobacterial PE and PPE proteins provide a framework for future research
4. PE_PGRS Antigens ofMycobacterium tuberculosisInduce Maturation and Activation of Human Dendritic Cells
5. Are the PE-PGRS proteins of Mycobacterium tuberculosis variable surface antigens?
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1. Impact of Growth Conditions on High-Throughput Identification of Repurposing Drugs for Pseudomonas aeruginosa Cystic Fibrosis Lung Infections;Antibiotics;2024-07-12
2. Mycobacterium tuberculosis PE_PGRS45 (Rv2615c) Promotes Recombinant Mycobacteria Intracellular Survival via Regulation of Innate Immunity, and Inhibition of Cell Apoptosis;Journal of Microbiology;2024-01
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