Bac-EPIC: A web interface for developing novel efflux pump inhibitor compounds targeting Escherichia coli

Q2 Medicine
Medicine in Drug Discovery Pub Date : 2023-12-01 Epub Date: 2023-10-26 DOI:10.1016/j.medidd.2023.100164
Shweta Singh Chauhan , Priyam Pandey , Sabrina Manickam , Ramakrishnan Parthasarathi
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引用次数: 0

Abstract

Multidrug resistance (MDR) poses a severe threat to human health. The existence of efflux pumps primarily contributes to resistance in Gram-negative bacterial infections. Efflux pump inhibitors (EPIs) can potentially improve the efficacy of antibiotics and reduce bacterial pathogenicity by inhibiting the mechanism of these pumps. Here we report Bac-EPIC, a web interface consisting of AcrA_Ipred, and AcrB_Ipred tools, can aid in the identification of potential EPIs that might bind to AcrAB-TolC pump subunits, alter its structure in vivo, prevent efflux, and enhance antibiotic efficacy in Escherichia coli (E. coli) and other Gram-negative bacteria. The web server is developed by collecting and archiving structural moieties from literature-reported EPIs. The web interface can be utilized in decision-making upon structural similarity-based screening on whether a compound should be examined experimentally or disregarded. It takes the SMILES format of chemical structure as an input. Users can also draw the 2D structure and get the output report of the possible structural similarity profile, similarity percentage, and the active moieties in the compound. The designed web interface is publicly accessible for in silico efflux pump inhibition prediction, at http://14.139.62.46/AcrAB_Ipred/. Overall, the webserver increases the diversity of EPIs, and proposes mechanistic insights to understand and regulate the efflux pump assembly & its function, ultimately aiding in fight against antibiotic resistance.

Abstract Image

Bac-EPIC:开发针对大肠杆菌的新型外排泵抑制剂化合物的web界面
多药耐药(MDR)严重威胁着人类健康。外排泵的存在主要有助于革兰氏阴性细菌感染的耐药性。外排泵抑制剂(EPIs)可以通过抑制外排泵的作用机制来提高抗生素的疗效,降低细菌的致病性。在这里,我们报道了Bac-EPIC,一个由AcrA_Ipred和AcrB_Ipred工具组成的网络界面,可以帮助鉴定可能结合AcrAB-TolC泵亚基的潜在epi,改变其体内结构,防止外排,并提高对大肠杆菌(E. coli)和其他革兰氏阴性菌的抗生素疗效。web服务器是通过收集和归档文献报道的EPIs结构片段而开发的,web界面可以用于基于结构相似性筛选化合物是否应该进行实验检查或忽略的决策。它以化学结构的SMILES格式作为输入。用户还可以绘制二维结构,并获得可能的结构相似曲线、相似百分比和化合物中活性成分的输出报告。设计的web界面是公开访问的硅外排泵抑制预测,在http://14.139.62.46/AcrAB_Ipred/。总体而言,网站服务器增加了epi的多样性,并提出了机制见解,以理解和调节外排泵组件。它的功能,最终帮助对抗抗生素耐药性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Medicine in Drug Discovery
Medicine in Drug Discovery Medicine-Pharmacology (medical)
CiteScore
8.30
自引率
0.00%
发文量
30
审稿时长
21 days
期刊介绍:
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