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Research Articles

Identification of potential novel inhibitors against glutamine synthetase enzyme of Leishmania major by using computational tools

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Pages 13914-13922 | Received 29 Nov 2022, Accepted 28 Jan 2023, Published online: 06 Feb 2023
 

Abstract

Glutamine Synthetase (GS) is functionally important in many pathogens, so its viability as a drug target has been widely investigated. We identified Leishmania major glutamine synthetase (Lm-GS) as an appealing target for developing potential leishmaniasis inhibitors. Comparative modeling, virtual screening, MD simulations along with MM-PBSA analyses were performed and two FDA approved compounds namely Chlortalidone (id ZINC00020253) and Ciprofloxacin (id ZINC00020220) were identified as potential inhibitor among the screened library. These compounds may be used as a lead molecule, although additional in vitro and in vivo testing is required to establish its anti-leishmanial effect. Hence, the goal of this study was to locate and identify certain medications that were previously FDA-approved for definite disorders and that might show anti-leishmanial effect. Due to GS's presence in additional Leishmania species, a novel medication docked with Lm-GS may have broad anti-leishmania efficacy.

Communicated by Ramaswamy H. Sarma

Acknowledgement

Mohammad Kashif is thankful to ICMR for providing Research Associate fellowship. Bioinformatics infrastructure facility at our school funded by Department of Biotechnology, Government of India.

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

The author(s) reported there is no funding associated with the work featured in this article.

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