In silico exploration of deep-sea fungal metabolites as inhibitor of Ebola and Marburg VP35 and VP40
Abdullah R. Alanzi,
Mohammed F. Alajmi,
Mohammed S. Al-Dosari
et al.
Abstract:VP30 and VP40 proteins of Ebola and Marburg viruses have been recognized as potential targets for antiviral drug development due to their essential roles in the viral lifecycle. Targeting these proteins could disrupt key stages of the viral replication process, inhibiting the viruses’ ability to propagate and cause disease. The current study aims to perform molecular docking and virtual screening on deep-sea fungal metabolites targeting Marburg virus VP40 Dimer, matrix protein VP40 from Ebola virus Sudan, Ebol… Show more
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