Department of Biomedical Engineering, The G.W.C. Whiting School of Engineering, Johns Hopkins University, Baltimore, MD 21218, USA.
Department of Biochemistry and Molecular Biology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD 21205, USA.
Nucleic Acids Res. 2021 Jan 8;49(D1):D261-D265. doi: 10.1093/nar/gkaa941.
ADP-ribosylation is a protein modification responsible for biological processes such as DNA repair, RNA regulation, cell cycle and biomolecular condensate formation. Dysregulation of ADP-ribosylation is implicated in cancer, neurodegeneration and viral infection. We developed ADPriboDB (adpribodb.leunglab.org) to facilitate studies in uncovering insights into the mechanisms and biological significance of ADP-ribosylation. ADPriboDB 2.0 serves as a one-stop repository comprising 48 346 entries and 9097 ADP-ribosylated proteins, of which 6708 were newly identified since the original database release. In this updated version, we provide information regarding the sites of ADP-ribosylation in 32 946 entries. The wealth of information allows us to interrogate existing databases or newly available data. For example, we found that ADP-ribosylated substrates are significantly associated with the recently identified human protein interaction networks associated with SARS-CoV-2, which encodes a conserved protein domain called macrodomain that binds and removes ADP-ribosylation. In addition, we create a new interactive tool to visualize the local context of ADP-ribosylation, such as structural and functional features as well as other post-translational modifications (e.g. phosphorylation, methylation and ubiquitination). This information provides opportunities to explore the biology of ADP-ribosylation and generate new hypotheses for experimental testing.
ADP-核糖基化是一种蛋白质修饰,负责多种生物学过程,如 DNA 修复、RNA 调控、细胞周期和生物分子凝聚体形成。ADP-核糖基化的失调与癌症、神经退行性疾病和病毒感染有关。我们开发了 ADPriboDB(adpribodb.leunglab.org),以促进研究揭示 ADP-核糖基化的机制和生物学意义。ADPriboDB 2.0 作为一个一站式存储库,包含 48346 项条目和 9097 种 ADP-核糖基化蛋白,其中 6708 种是自原始数据库发布以来新发现的。在这个更新版本中,我们提供了 32946 项条目中 ADP-核糖基化位点的信息。丰富的信息使我们能够查询现有的数据库或新可用的数据。例如,我们发现 ADP-核糖基化的底物与最近发现的与 SARS-CoV-2 相关的人类蛋白质相互作用网络显著相关,该网络编码一个称为宏结构域的保守蛋白结构域,它可以结合并去除 ADP-核糖基化。此外,我们创建了一个新的交互式工具,用于可视化 ADP-核糖基化的局部上下文,例如结构和功能特征以及其他翻译后修饰(如磷酸化、甲基化和泛素化)。这些信息为探索 ADP-核糖基化的生物学提供了机会,并为实验测试生成了新的假设。