التفاصيل البيبلوغرافية
| العنوان: |
Experimental and computational insights of Albizia amara phytoconstituents targeting anthranilate phosphoribosyltransferase from Malassezia globosa. |
| المؤلفون: |
Subhashini, Ramakrishnan1 (AUTHOR) subhashini.r@grd.edu.in, Jebastin, Thomas1,2 (AUTHOR) jebastin.bi@bhc.edu.in, Khasamwala, Abbas M1 (AUTHOR), Al-Anazi, Khalid Mashay3 (AUTHOR), Farah, Mohammad Abul3 (AUTHOR), Jeyam, Muthusamy1,4 (AUTHOR) jeyam@buc.edu.in |
| المصدر: |
Acta Tropica. Nov2024, Vol. 259, pN.PAG-N.PAG. 1p. |
| مصطلحات موضوعية: |
*DERMATOMYCOSES, *BIOACTIVE compounds, *BINDING energy, *DRUG target, *MOLECULAR docking, *ANTIFUNGAL agents |
| مستخلص: |
• Commensals transit as pathogens, associated with dermatological conditions. • Targeted specific enzyme exists only in pathogen metabolic pathway. • Phytoconstituents inducing the antifungal activity signifies the remedy. • Computational approaches ascertain the prominent compound against the target. The fungus Malassezia globosa is often responsible for superficial mycoses posing significant treatment challenges because of the unfavourable side effects of available antifungal drugs. To reduce potential hazards to the host and overcome these hurdles, new therapeutic medicines must be developed that selectively target enzymes unique to the pathogen. This study focuses on the enzyme anthranilate phosphoribosyltransferase (AnPRT), which is vital to M. globosa 's tryptophan production pathway. To learn more about the function of the AnPRT enzyme, we modeled, validated, and simulated its structure. Moreover, many bioactive components were found in different extracts from the plant Albizia amara after phytochemical screening. Interestingly, at doses ranging from 500 to 2000 µg/ml, the chloroform extract showed significant antifungal activity, with inhibition zones measured between 11.0 ± 0.0 and 25.6 ± 0.6 mm. According to molecular docking analyses, the compounds from the active extract, particularly 2-tert-Butyl-4-isopropyl-5-methylphenol, interacted with the AnPRT enzyme's critical residues, ARG 205 and PHE 214, with an effective binding energy of -4.9 kcal/mol. The extract's revealed component satisfies the requirements for drug-likeness and shows promise as a strong antifungal agent against infections caused by M. globosa. These findings imply that using plant-derived chemicals to target the AnPRT enzyme is a viable path for the creation of innovative antifungal treatments. [ABSTRACT FROM AUTHOR] |
| قاعدة البيانات: |
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