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iEKPD 2.0:具有丰富注释的真核蛋白激酶、蛋白磷酸酶和含磷酸化蛋白结合域蛋白的更新版本。

iEKPD 2.0: an update with rich annotations for eukaryotic protein kinases, protein phosphatases and proteins containing phosphoprotein-binding domains.

机构信息

Department of Bioinformatics & Systems Biology, Key Laboratory of Molecular Biophysics of Ministry of Education, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074, China.

出版信息

Nucleic Acids Res. 2019 Jan 8;47(D1):D344-D350. doi: 10.1093/nar/gky1063.

DOI:10.1093/nar/gky1063
PMID:30380109
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6324023/
Abstract

Here, we described the updated database iEKPD 2.0 (http://iekpd.biocuckoo.org) for eukaryotic protein kinases (PKs), protein phosphatases (PPs) and proteins containing phosphoprotein-binding domains (PPBDs), which are key molecules responsible for phosphorylation-dependent signalling networks and participate in the regulation of almost all biological processes and pathways. In total, iEKPD 2.0 contained 197 348 phosphorylation regulators, including 109 912 PKs, 23 294 PPs and 68 748 PPBD-containing proteins in 164 eukaryotic species. In particular, we provided rich annotations for the regulators of eight model organisms, especially humans, by compiling and integrating the knowledge from 100 widely used public databases that cover 13 aspects, including cancer mutations, genetic variations, disease-associated information, mRNA expression, DNA & RNA elements, DNA methylation, molecular interactions, drug-target relations, protein 3D structures, post-translational modifications, protein expressions/proteomics, subcellular localizations and protein functional annotations. Compared with our previously developed EKPD 1.0 (∼0.5 GB), iEKPD 2.0 contains ∼99.8 GB of data with an ∼200-fold increase in data volume. We anticipate that iEKPD 2.0 represents a more useful resource for further study of phosphorylation regulators.

摘要

在这里,我们描述了经过更新的真核蛋白激酶(PKs)、蛋白磷酸酶(PPs)和含有磷酸化蛋白结合域(PPBDs)的蛋白质数据库 iEKPD 2.0(http://iekpd.biocuckoo.org),这些是负责磷酸化依赖信号网络的关键分子,参与了几乎所有生物过程和途径的调控。总的来说,iEKPD 2.0 包含了 197348 个磷酸化调控因子,包括 164 个真核物种中的 109912 个 PKs、23294 个 PPs 和 68748 个含有 PPBD 的蛋白质。特别是,我们通过整合 100 个广泛使用的公共数据库中的知识,为八个模式生物(特别是人类)的调控因子提供了丰富的注释,这些数据库涵盖了癌症突变、遗传变异、疾病相关信息、mRNA 表达、DNA 和 RNA 元件、DNA 甲基化、分子相互作用、药物靶点关系、蛋白质 3D 结构、翻译后修饰、蛋白质表达/蛋白质组学、亚细胞定位和蛋白质功能注释等 13 个方面。与我们之前开发的 EKPD 1.0(约 0.5GB)相比,iEKPD 2.0 包含约 99.8GB 的数据,数据量增加了约 200 倍。我们预计 iEKPD 2.0 将成为进一步研究磷酸化调控因子的更有用的资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb78/6324023/8ee5b2ab0b73/gky1063fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb78/6324023/84195cdf2436/gky1063fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb78/6324023/db9f5d0c408f/gky1063fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb78/6324023/faace7283409/gky1063fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb78/6324023/8ee5b2ab0b73/gky1063fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb78/6324023/84195cdf2436/gky1063fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb78/6324023/db9f5d0c408f/gky1063fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb78/6324023/faace7283409/gky1063fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb78/6324023/8ee5b2ab0b73/gky1063fig4.jpg

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