Oregon Health & Science University, Portland, Oregon.
NYU Langone Health, New York, New York.
Curr Protoc. 2023 Jul;3(7):e845. doi: 10.1002/cpz1.845.
Understudied or dark proteins have the potential to shed light on as-yet undiscovered molecular mechanisms that underlie phenotypes and suggest innovative therapeutic approaches for many diseases. The Reactome-IDG (Illuminating the Druggable Genome) project aims to place dark proteins in the context of manually curated, highly reliable pathways in Reactome, the most comprehensive, open-source biological pathway knowledgebase, facilitating the understanding functions and predicting therapeutic potentials of dark proteins. The Reactome-IDG web portal, deployed at https://idg.reactome.org, provides a simple, interactive web page for users to search pathways that may functionally interact with dark proteins, enabling the prediction of functions of dark proteins in the context of Reactome pathways. Enhanced visualization features implemented at the portal allow users to investigate the functional contexts for dark proteins based on tissue-specific gene or protein expression, drug-target interactions, or protein or gene pairwise relationships in the original Reactome's systems biology graph notation (SBGN) diagrams or the new simplified functional interaction (FI) network view of pathways. The protocols in this chapter describe step-by-step procedures to use the web portal to learn biological functions of dark proteins in the context of Reactome pathways. © 2023 Wiley Periodicals LLC. Basic Protocol 1: Search for interacting pathways of a protein Support Protocol: Interacting pathway results for an annotated protein Alternate Protocol: Use individual pairwise relationships to predict interacting pathways of a protein Basic Protocol 2: Using the IDG pathway browser to study interacting pathways Basic Protocol 3: Overlaying tissue-specific expression data Basic Protocol 4: Overlaying protein/gene pairwise relationships in the pathway context Basic Protocol 5: Visualizing drug/target interactions.
未被充分研究或未知的蛋白质有可能揭示尚未被发现的潜在分子机制,这些机制是许多疾病表型的基础,并为许多疾病提供创新的治疗方法。Reactome-IDG(照亮可成药基因组)项目旨在将暗蛋白置于 Reactome 中手工整理的、高度可靠的途径背景下,Reactome 是最全面的开源生物途径知识库,有助于理解暗蛋白的功能并预测其治疗潜力。Reactome-IDG 门户网站部署在 https://idg.reactome.org,为用户提供了一个简单的交互网页,用于搜索可能与暗蛋白功能相互作用的途径,从而可以预测暗蛋白在 Reactome 途径中的功能。该门户实施的增强可视化功能允许用户根据组织特异性基因或蛋白质表达、药物靶点相互作用或蛋白质或基因在原始 Reactome 的系统生物学图形表示法 (SBGN) 图或新的简化功能相互作用 (FI) 途径网络视图中的成对关系,研究暗蛋白的功能背景。本章中的方案描述了使用门户网站在 Reactome 途径的背景下学习暗蛋白生物学功能的逐步过程。© 2023 Wiley Periodicals LLC。基础方案 1:搜索蛋白质相互作用的途径 支持方案:注释蛋白质的相互作用途径结果 备选方案:使用单个成对关系预测蛋白质的相互作用途径 基础方案 2:使用 IDG 途径浏览器研究相互作用的途径 基础方案 3:叠加组织特异性表达数据 基础方案 4:在途径上下文中叠加蛋白质/基因成对关系 基础方案 5:可视化药物/靶点相互作用。