• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

KINAID:一种用于磷酸蛋白质组学的基于直系同源的激酶-底物预测与分析工具。

KINAID: an orthology-based kinase-substrate prediction and analysis tool for phosphoproteomics.

作者信息

Aman Javed M, Zhu Audrey W, Wühr Martin, Shvartsman Stanislav Y, Singh Mona

机构信息

Computer Science Department, Princeton University, Princeton, NJ, 08544, United States.

Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, 08544, United States.

出版信息

Bioinformatics. 2025 May 6;41(5). doi: 10.1093/bioinformatics/btaf300.

DOI:10.1093/bioinformatics/btaf300
PMID:40347463
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12122078/
Abstract

SUMMARY

Proteome-wide datasets of phosphorylated peptides, either measured in a condition of interest or in response to perturbations, are increasingly becoming available for model organisms across the evolutionary spectrum. We introduce KINAID (KINase Activity and Inference Dashboard), an interactive and extensible tool written in Dash/Plotly, that predicts kinase-substrate interactions, uncovers and displays kinases whose substrates are enriched amongst phosphorylated peptides, interactively illustrates kinase-substrate interactions, and clusters phosphopeptides targeted by similar kinases. KINAID is the first tool of its kind that can analyze data from not only Homo sapiens but also 10 additional model organisms (including Mus musculus, Danio rerio, Drosophila melanogaster, Caenorhabditis elegans, and Saccharomyces cerevisiae). We demonstrate KINAID's utility by applying it to recently published S. cerevisiae phosphoproteomics data.

AVAILABILITY AND IMPLEMENTATION

Webserver is available at https://kinaid.princeton.edu; open-source python library is available at https://github.com/Singh-Lab/kinaid; archive is available at https://doi.org/10.24433/CO.8460107.v1.

摘要

摘要

在整个进化谱系的模式生物中,无论是在感兴趣的条件下测量还是响应扰动而测量的磷酸化肽的全蛋白质组数据集越来越多。我们引入了KINAID(激酶活性和推理仪表板),这是一个用Dash/Plotly编写的交互式可扩展工具,它可以预测激酶-底物相互作用,发现并显示其底物在磷酸化肽中富集的激酶,以交互方式说明激酶-底物相互作用,并对相似激酶靶向的磷酸肽进行聚类。KINAID是同类工具中的第一个,它不仅可以分析来自智人的数据,还可以分析另外10种模式生物(包括小家鼠、斑马鱼、黑腹果蝇、秀丽隐杆线虫和酿酒酵母)的数据。我们通过将KINAID应用于最近发表的酿酒酵母磷酸蛋白质组学数据来证明其效用。

可用性和实现方式

网络服务器可在https://kinaid.princeton.edu获得;开源Python库可在https://github.com/Singh-Lab/kinaid获得;存档可在https://doi.org/10.24433/CO.8460107.v1获得。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ab/12122078/ebaa8d9b8648/btaf300f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ab/12122078/ebaa8d9b8648/btaf300f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ab/12122078/ebaa8d9b8648/btaf300f1.jpg

相似文献

1
KINAID: an orthology-based kinase-substrate prediction and analysis tool for phosphoproteomics.KINAID:一种用于磷酸蛋白质组学的基于直系同源的激酶-底物预测与分析工具。
Bioinformatics. 2025 May 6;41(5). doi: 10.1093/bioinformatics/btaf300.
2
PhosX: data-driven kinase activity inference from phosphoproteomics experiments.PhosX:基于磷酸化蛋白质组学实验的数据驱动激酶活性推断
Bioinformatics. 2024 Nov 28;40(12). doi: 10.1093/bioinformatics/btae697.
3
Positive-unlabeled ensemble learning for kinase substrate prediction from dynamic phosphoproteomics data.基于动态磷酸化蛋白质组学数据的激酶底物预测的正例-未标记样本集成学习
Bioinformatics. 2016 Jan 15;32(2):252-9. doi: 10.1093/bioinformatics/btv550. Epub 2015 Sep 22.
4
Protein kinases associated with the yeast phosphoproteome.与酵母磷酸化蛋白质组相关的蛋白激酶。
BMC Bioinformatics. 2006 Jan 31;7:47. doi: 10.1186/1471-2105-7-47.
5
Phosphoproteomics-Based Profiling of Kinase Activities in Cancer Cells.基于磷酸化蛋白质组学的癌细胞激酶活性分析
Methods Mol Biol. 2018;1711:103-132. doi: 10.1007/978-1-4939-7493-1_6.
6
msproteomics sitereport: reporting DIA-MS phosphoproteomics experiments at site level with ease.ms 蛋白质组学站点报告:轻松实现基于 DIA-MS 的磷酸化蛋白质组学实验的站点级报告。
Bioinformatics. 2024 Jul 1;40(7). doi: 10.1093/bioinformatics/btae432.
7
Phosphoproteome resource for systems biology research.用于系统生物学研究的磷酸化蛋白质组资源。
Methods Mol Biol. 2011;694:307-22. doi: 10.1007/978-1-60761-977-2_19.
8
Phosphoproteomics Meets Chemical Genetics: Approaches for Global Mapping and Deciphering the Phosphoproteome.磷酸化蛋白质组学与化学遗传学的交汇:全球磷酸蛋白质组图谱绘制与解读的方法。
Int J Mol Sci. 2020 Oct 15;21(20):7637. doi: 10.3390/ijms21207637.
9
IKAP: A heuristic framework for inference of kinase activities from Phosphoproteomics data.IKAP:一种从磷酸化蛋白质组学数据推断激酶活性的启发式框架。
Bioinformatics. 2016 Feb 1;32(3):424-31. doi: 10.1093/bioinformatics/btv699. Epub 2015 Dec 1.
10
Biotinylated phosphoproteins from kinase-catalyzed biotinylation are stable to phosphatases: implications for phosphoproteomics.激酶催化生物素化的生物素化磷酸蛋白对磷酸酶稳定:对磷酸蛋白质组学的影响。
Chembiochem. 2013 Feb 11;14(3):381-7. doi: 10.1002/cbic.201200626. Epub 2013 Jan 17.

本文引用的文献

1
The intrinsic substrate specificity of the human tyrosine kinome.人类酪氨酸激酶组的固有底物特异性。
Nature. 2024 May;629(8014):1174-1181. doi: 10.1038/s41586-024-07407-y. Epub 2024 May 8.
2
The regulatory landscape of the yeast phosphoproteome.酵母磷酸化组的调控格局。
Nat Struct Mol Biol. 2023 Nov;30(11):1761-1773. doi: 10.1038/s41594-023-01115-3. Epub 2023 Oct 16.
3
Positive feedback induces switch between distributive and processive phosphorylation of Hog1.正反馈诱导 Hog1 的分布式磷酸化和连续磷酸化之间的转换。
Nat Commun. 2023 Apr 29;14(1):2477. doi: 10.1038/s41467-023-37430-y.
4
Protein phosphorylation database and prediction tools.蛋白质磷酸化数据库及预测工具。
Brief Bioinform. 2023 Mar 19;24(2). doi: 10.1093/bib/bbad090.
5
An atlas of substrate specificities for the human serine/threonine kinome.人类丝氨酸/苏氨酸激酶组的底物特异性图谱
Nature. 2023 Jan;613(7945):759-766. doi: 10.1038/s41586-022-05575-3. Epub 2023 Jan 11.
6
Inferring kinase activity from phosphoproteomic data: Tool comparison and recent applications.从磷酸化蛋白质组学数据推断激酶活性:工具比较与近期应用
Mass Spectrom Rev. 2024 Jul-Aug;43(4):725-751. doi: 10.1002/mas.21808. Epub 2022 Sep 26.
7
dbPTM in 2022: an updated database for exploring regulatory networks and functional associations of protein post-translational modifications.dbPTM 在 2022 年:一个更新的数据库,用于探索蛋白质翻译后修饰的调控网络和功能关联。
Nucleic Acids Res. 2022 Jan 7;50(D1):D471-D479. doi: 10.1093/nar/gkab1017.
8
Robust inference of kinase activity using functional networks.使用功能网络进行激酶活性的稳健推断。
Nat Commun. 2021 Feb 19;12(1):1177. doi: 10.1038/s41467-021-21211-6.
9
Sequence and Structure-Based Analysis of Specificity Determinants in Eukaryotic Protein Kinases.基于序列和结构的真核蛋白激酶特异性决定因素分析。
Cell Rep. 2021 Jan 12;34(2):108602. doi: 10.1016/j.celrep.2020.108602.
10
Using phosphoproteomics data to understand cellular signaling: a comprehensive guide to bioinformatics resources.利用磷酸化蛋白质组学数据理解细胞信号传导:生物信息学资源综合指南
Clin Proteomics. 2020 Jul 11;17:27. doi: 10.1186/s12014-020-09290-x. eCollection 2020.