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Potential of Mycobacterium tuberculosis Type II NADH-Dehydrogenase in Antitubercular Drug Discovery.
- Source :
-
ACS infectious diseases [ACS Infect Dis] 2025 Feb 14; Vol. 11 (2), pp. 398-412. Date of Electronic Publication: 2025 Jan 15. - Publication Year :
- 2025
-
Abstract
- The type II NADH-dehydrogenase enzyme in Mycobacterium tuberculosis plays a critical role in the efficient functioning of the oxidative phosphorylation pathway. It acts as the entry point for electrons in the electron transport chain, which is essential for fulfilling the energy requirements of both replicating and nonreplicating mycobacterial species. Due to the absence of the type II NADH-dehydrogenase enzyme in mammalian mitochondria, targeting the type II NADH-dehydrogenase enzyme for antitubercular drug discovery could be a vigilant approach. Utilizing type II NADH-dehydrogenase inhibitors in antitubercular therapy led to bactericidal response, even in monotherapy. However, the absence of the cryo-EM structure of Mycobacterium tuberculosis type II NADH-dehydrogenase has constrained drug discovery efforts to rely on high-throughput screening methods, limiting the use of structure-based drug discovery. Here, we have delineated the literature-reported Mycobacterium tuberculosis type II NADH-dehydrogenase inhibitors and the rationale behind selecting this specific enzyme for antitubercular drug discovery, along with shedding light on the architecture of the enzyme structure and functionality. The gap in the current research and future research direction for TB treatment have been addressed.
- Subjects :
- Humans
Enzyme Inhibitors pharmacology
Enzyme Inhibitors chemistry
Bacterial Proteins metabolism
Bacterial Proteins antagonists & inhibitors
Bacterial Proteins chemistry
Tuberculosis drug therapy
Tuberculosis microbiology
Mycobacterium tuberculosis enzymology
Mycobacterium tuberculosis drug effects
Antitubercular Agents pharmacology
Antitubercular Agents chemistry
Drug Discovery
NADH Dehydrogenase antagonists & inhibitors
NADH Dehydrogenase metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2373-8227
- Volume :
- 11
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- ACS infectious diseases
- Publication Type :
- Academic Journal
- Accession number :
- 39812155
- Full Text :
- https://doi.org/10.1021/acsinfecdis.4c01005