Fragment-based design and MD simulations of human papilloma virus-16 E6 protein inhibitors.

The main objective of this study is to screen potential small molecule inhibitors against HPV (Human Papilloma Virus)-16 E6 protein (HPV16 E6P) using a fragment-based approach. Twenty-six natural HPV inhibitors were selected based on the review of the literature. Among them, Luteolin was selected as the reference compound.

Analysis of Natural Inhibitors against HPV E6 Protein.

Background: Drug re-purposing is one of the cost-effective methods to establish novel therapeutics against many diseases. Established natural products are collected from databases and used to potentially screen them against HPV E6 protein, a critical viral protein.

Objective: This study aims to design potential small molecule inhibitors against HPV E6 protein using structure-based approaches.