Molecular Network Simulation of Bawang Ada’ (Eleutherine americana Merr.) from Dayak Lundayeh in North Kalimantan Tackle various Viral Infection Targeting Key Protein

Viol Dhea Kharisma, Priscilla Listiyani, Ahmad Affan Ali Murtadlo, Rizal Adistya Putra Pradana, A. N.M. Ansori, Alexander Patera Nugraha, Rollando Rollando, Raden Joko Kuncoroningrat Susilo, Suhailah Hayaza, Sofya Olegovna Budagova, Gregory Vadimovich Nadvodnyk, Ivan Gennadievich Lebedev, Zaira Nadirovna Khalibekova, Igor Vladimirovich Rzhepakovsky, Maksim Rebezov, Vikash Jakhmola, Hery Purnobasuki, Dwi Kusuma Wahyuni

Research output: Contribution to journalArticlepeer-review

Abstract

Viral replication inhibition strategies are needed to prevent pandemics through the latest therapeutic agent designs. A viral infection occurring over a wide area is called a pandemic. The strategy of inhibiting virus replication is used to tackle the pandemic Viruses can trigger negative regulation of apoptosis in host cells for viral survival. Apoptosis can reduce viral load and inhibit viral replication. Several types of viruses can evade the immune response through upregulation of various anti-apoptotic proteins, which allows this research to explore specific types of anti-apoptotic proteins in host cells for the design of candidate therapeutic agents. Medicinal plants from the Dayak Lundayeh tribe in North Kalimantan have potential for health, the antiviral potential of these plants has not been identified. This study aims to reveal the potential of the bioactive compounds from Bawang Ada' as antivirals with a molecular mechanism through apoptosis with an in silico approach. The in silico method used in this study consisted of ligand preparation, druglikeness analysis, pathway prediction, docking, and molecular interaction. Bawang Ada' acts as the best antiviral candidate through the activity of Erythrolaccin and Isoeleutherin compounds in inhibiting antiapoptotic proteins consisting of GSK3B and AKT1. We recommend the binding sites Val70, Leu132, Ile62, Leu188, Asp200, and Cys199 (GSK3B) and Leu210, Leu264, Tyr272, Asp292, Trp80, Lys 268, Val270, and Ser205 (AKT1) for further research as antiviral target development.

Original languageEnglish
Pages (from-to)1961-1967
Number of pages7
JournalResearch Journal of Pharmacy and Technology
Volume17
Issue number5
DOIs
Publication statusPublished - 2024

Keywords

  • Antiviral
  • Apoptosis Agonist
  • Bawang Ada’
  • Bioinformatics
  • Eleutherine americana

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