Molecular docking study of Lens culinaris L. phytochemicals to NS3-NS2B protease of dengue virus serotype 2

Journal Title: German Journal of Microbiology - Year 2021, Vol 1, Issue 1

Abstract

Forty-three phytochemicals present in Lens culinaris were evaluated through in silico molecular docking studies for their binding affinities to the NS2B-NS3 activator-protease complex of dengue virus serotype 2 (DENV-2). Among the various compounds tested, flavonoids (flavanols, flavonols, proanthocyanidins, flavanones, flavones, and anthocyanins) demonstrated high binding affinities for the protease complex. Eriodictyol-7-O-rutinoside showed the least predicted binding energy at -9.1 kcal/mol followed by luteolin-7-O-glucoside at -8.8 kcal/mol. Glycosidic linkages appeared to enhance the binding affinities of flavonoids, aldohexoses being more potent than aldopentoses. Besides flavonoids, other classes of compounds demonstrating high binding affinities for the protease were carotenoids, phytosterols, and polyphenolic compounds like resveratrol and trans-resveratrol 3-O-b-glucoside (piceid), the latter showing predicted binding energy of -8.5 kcal/mol versus predicted binding energy of -7.2 kcal/mol for resveratrol. 2D interactions of four high binding affinity compounds like eriodictyol, eriodictyol-7-O-rutinoside, catechin gallate, and luteolin-7-O-glucoside showed that all four compounds bound to the active site of the NS3 protease and not to the activator NS2B. Lys74 of NS3 was the common amino acid interacting with all four phytochemicals. Analysis of physicochemical properties of the compounds (Lipinski’s Rule of 5) showed that the high binding affinity compounds all have less than two violations, indicating that they can serve as useful lead compounds or as dengue virus serotype 2 therapeutics.

Authors and Affiliations

Tohmina Afroze Bondhon, Anamul Hasan, Khoshnur Jannat, Alok Paul, Rownak Jahan, Tooba Mahboob, Veeranoot Nissapatorn, Karma G Dolma, Maria L. Pereira, Christophe Wiart and Mohammed Rahmatullah

Keywords

Related Articles

The German Journal of Microbiology; towards dissemination and globalization of microbiology research

The emergence and re-emergence of diseases pose serious challenges to the global community, giving a wake-up call for the entire scientific community to collaborate to understand the nature of microorganisms and control...

Emerging carbapenem resistance in ESKAPE organisms in sub-Saharan Africa and the way forward

The epidemiology of Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter species (ESKAPE) and their role in the development and spread of m...

Susceptibility of extended-spectrum β-lactamase (ESBL) producing Enterobacteriaceae to Roundup

Bacteria and other microorganisms have several mechanisms to react to stress in the environment. Exposure of bacteria to antibiotics, biocides, or selective pressure may favor the emergence of antimicrobial resistance by...

Klebsiella pneumoniae in Germany: An overview on spatiotemporal distribution and resistance development in humans

The emerging of multidrug-resistant Klebsiella pneumoniae (K. pneumoniae) is increasing worldwide. Rapid dissemination and increase of its incidence in Germany are observed and becoming a significant challenge for clinic...

Molecular docking study of Lens culinaris L. phytochemicals to NS3-NS2B protease of dengue virus serotype 2

Forty-three phytochemicals present in Lens culinaris were evaluated through in silico molecular docking studies for their binding affinities to the NS2B-NS3 activator-protease complex of dengue virus serotype 2 (DENV-2)....

Download PDF file
  • EP ID EP696841
  • DOI https://doi.org/10.51585/gjm.2021.0005
  • Views 116
  • Downloads 0

How To Cite

Tohmina Afroze Bondhon, Anamul Hasan, Khoshnur Jannat, Alok Paul, Rownak Jahan, Tooba Mahboob, Veeranoot Nissapatorn, Karma G Dolma, Maria L. Pereira, Christophe Wiart and Mohammed Rahmatullah (2021). Molecular docking study of Lens culinaris L. phytochemicals to NS3-NS2B protease of dengue virus serotype 2. German Journal of Microbiology, 1(1), -. https://europub.co.uk/articles/-A-696841