Protein Visualizer 2.0: Intuitive and Interactive Visualization of Protein Topology and Co/Post-Translational Modifications

IF 3.8 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Manthan Desai,  and , Bingyun Sun*, 
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引用次数: 0

Abstract

Topology and post-translational modifications (PTMs) are critical features in studying the structures and functions of proteins. Several popular and detailed protein visualization algorithms are available for such studies, such as PyMOL, NCBI’s iCn3D, UniProt PTM viewing, and Protter. However, none of the studies depict the special relationships between key structural features such as N-glycosylation, disulfide bonds, potential N-glycosylation sites (free sequons), potential disulfide bonds (free cysteine sites), and protein topology in a way conducive to detailed analyses. We introduce Protein Visualizer 2.0 (https://sfu-sun-lab.github.io/protein-visualizer-2.0/), a web-based tool that visualizes these features and the topology of all human proteins. This tool allows users to readily assess potential conflicts among predicted protein topology and known co/post-translational modifications. This tool also helps to reveal hidden relationships among displayed structural features.

Abstract Image

Protein Visualizer 2.0:蛋白质拓扑和共/翻译后修饰的直观互动可视化
拓扑结构和翻译后修饰(PTM)是研究蛋白质结构和功能的关键特征。目前有几种流行的详细蛋白质可视化算法可用于此类研究,如 PyMOL、NCBI 的 iCn3D、UniProt PTM 查看和 Protter。然而,这些研究都没有以有利于详细分析的方式描述关键结构特征之间的特殊关系,如 N-糖基化、二硫键、潜在的 N-糖基化位点(游离序列)、潜在的二硫键(游离半胱氨酸位点)和蛋白质拓扑结构。我们介绍了 Protein Visualizer 2.0 (https://sfu-sun-lab.github.io/protein-visualizer-2.0/),这是一种基于网络的工具,可将这些特征和所有人类蛋白质的拓扑结构可视化。该工具允许用户随时评估预测的蛋白质拓扑结构与已知的共翻译/翻译后修饰之间的潜在冲突。该工具还有助于揭示所显示的结构特征之间的隐藏关系。
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
ACS Chemical Biology
ACS Chemical Biology 生物-生化与分子生物学
CiteScore
7.50
自引率
5.00%
发文量
353
审稿时长
3.3 months
期刊介绍: ACS Chemical Biology provides an international forum for the rapid communication of research that broadly embraces the interface between chemistry and biology. The journal also serves as a forum to facilitate the communication between biologists and chemists that will translate into new research opportunities and discoveries. Results will be published in which molecular reasoning has been used to probe questions through in vitro investigations, cell biological methods, or organismic studies. We welcome mechanistic studies on proteins, nucleic acids, sugars, lipids, and nonbiological polymers. The journal serves a large scientific community, exploring cellular function from both chemical and biological perspectives. It is understood that submitted work is based upon original results and has not been published previously.
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