Thai Quynh Mai, Phung Huong T T, Pham Ngoc Quynh Anh, Horng Jim-Tong, Tran Phuong-Thao, Tung Nguyen Thanh, Ngo Son Tung
Laboratory of Biophysics, Institute for Advanced Study in Technology, Ton Duc Thang University, Ho Chi Minh City, Vietnam.
Faculty of Pharmacy, Ton Duc Thang University, Ho Chi Minh City, Vietnam.
J Biomol Struct Dyn. 2024 Feb 28:1-9. doi: 10.1080/07391102.2024.2321509.
VP39, an essential 2'-O-RNA methyltransferase enzyme discovered in Monkeypox virus (MPXV), plays a vital role in viral RNA replication and transcription. Inhibition of the enzyme may prevent viral replication. In this context, using a combination of molecular docking and molecular dynamics (MDs) simulations, the inhibitory ability of NCI Diversity Set VII natural compounds to VP39 protein was investigated. It should be noted that the computed binding free energy of ligand molecular docking and linear interaction energy (LIE) approaches are in good agreement with the corresponding experiments with coefficients of and 0.75, respectively. NSC 319990, NSC 196515 and NSC 376254 compounds were demonstrated that can inhibit MPVX methyltransferase VP39 protein with the similar affinity compared to available inhibitor sinefungin. Moreover, nine residues involving , , , , , , , and may be argued that they play an important role in binding process of inhibitors to VP39.
VP39是在猴痘病毒(MPXV)中发现的一种必需的2'-O-RNA甲基转移酶,在病毒RNA复制和转录中起着至关重要的作用。抑制该酶可能会阻止病毒复制。在此背景下,结合分子对接和分子动力学(MDs)模拟,研究了美国国立癌症研究所(NCI)多样性集VII天然化合物对VP39蛋白的抑制能力。需要注意的是,通过配体分子对接计算的结合自由能和线性相互作用能(LIE)方法与相应实验结果吻合良好,系数分别为 和0.75。已证明化合物NSC 319990、NSC 196515和NSC 376254与现有抑制剂西奈芬净相比,能以相似的亲和力抑制MPVX甲基转移酶VP39蛋白。此外,涉及 、 、 、 、 、 、 、 和 的九个残基可能在抑制剂与VP39的结合过程中发挥重要作用。