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DisCanVis:可视化整合的结构和功能注释,以更好地理解位于无序蛋白质内的癌症突变的影响。

DisCanVis: Visualizing integrated structural and functional annotations to better understand the effect of cancer mutations located within disordered proteins.

机构信息

Department of Biochemistry, Institute of Biology, ELTE Eötvös Loránd University, Budapest, Hungary.

出版信息

Protein Sci. 2023 Jan;32(1):e4522. doi: 10.1002/pro.4522.

DOI:10.1002/pro.4522
PMID:36452990
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9793970/
Abstract

Intrinsically disordered proteins (IDPs) play important roles in a wide range of biological processes and have been associated with various diseases, including cancer. In the last few years, cancer genome projects have systematically collected genetic variations underlying multiple cancer types. In parallel, the number and different types of disordered proteins characterized by experimental methods have also significantly increased. Nevertheless, the role of IDPs in various types of cancer is still not well understood. In this work, we present DisCanVis, a novel visualization tool for cancer mutations with a special focus on IDPs. In order to aid the interpretation of observed mutations, genome level information is combined with information about the structural and functional properties of proteins. The web server enables users to inspect individual proteins, collect examples with existing annotations of protein disorder and associated function or to discover currently uncharacterized examples with likely disease relevance. Through a REST API interface and precompiled tables the analysis can be extended to a group of proteins.

摘要

无规卷曲蛋白质(IDPs)在广泛的生物过程中发挥着重要作用,并与各种疾病相关,包括癌症。在过去的几年中,癌症基因组项目已经系统地收集了多种癌症类型的遗传变异。与此同时,通过实验方法鉴定的无序蛋白质的数量和类型也显著增加。然而,IDPs 在各种类型癌症中的作用仍未被很好地理解。在这项工作中,我们提出了 DisCanVis,这是一种针对癌症突变的新型可视化工具,特别关注无规卷曲蛋白质。为了帮助解释观察到的突变,我们将基因组水平的信息与蛋白质结构和功能特性的信息相结合。该网络服务器允许用户检查单个蛋白质,收集具有现有蛋白质无序性和相关功能注释的示例,或者发现具有潜在疾病相关性但目前尚未表征的示例。通过 REST API 接口和预编译的表格,可以将分析扩展到一组蛋白质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83d4/9793970/bb8a5cd906ad/PRO-32-e4522-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83d4/9793970/046d547b25a3/PRO-32-e4522-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83d4/9793970/cb1fcb05076a/PRO-32-e4522-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83d4/9793970/90318a479a1a/PRO-32-e4522-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83d4/9793970/ef282426a11a/PRO-32-e4522-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83d4/9793970/bb8a5cd906ad/PRO-32-e4522-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83d4/9793970/046d547b25a3/PRO-32-e4522-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83d4/9793970/cb1fcb05076a/PRO-32-e4522-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83d4/9793970/90318a479a1a/PRO-32-e4522-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83d4/9793970/ef282426a11a/PRO-32-e4522-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83d4/9793970/bb8a5cd906ad/PRO-32-e4522-g005.jpg

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本文引用的文献

1
Phase separation driven by interchangeable properties in the intrinsically disordered regions of protein paralogs.由蛋白质同源物无规则区域的可互换特性驱动的相分离。
Commun Biol. 2022 Apr 29;5(1):400. doi: 10.1038/s42003-022-03354-4.
2
Pan-cancer assessment of mutational landscape in intrinsically disordered hotspots reveals potential driver genes.泛癌症分析内在无序热点区的突变景观揭示潜在的驱动基因。
Nucleic Acids Res. 2022 May 20;50(9):e49. doi: 10.1093/nar/gkac028.
3
Ensembl 2022.Ensembl 2022.
Nucleic Acids Res. 2022 Jan 7;50(D1):D988-D995. doi: 10.1093/nar/gkab1049.
4
AlphaFold Protein Structure Database: massively expanding the structural coverage of protein-sequence space with high-accuracy models.AlphaFold 蛋白质结构数据库:用高精度模型极大地扩展蛋白质序列空间的结构覆盖范围。
Nucleic Acids Res. 2022 Jan 7;50(D1):D439-D444. doi: 10.1093/nar/gkab1061.
5
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.
6
The Eukaryotic Linear Motif resource: 2022 release.真核线性基序资源:2022 年版。
Nucleic Acids Res. 2022 Jan 7;50(D1):D497-D508. doi: 10.1093/nar/gkab975.
7
RAF1 amplification drives a subset of bladder tumors and confers sensitivity to MAPK-directed therapeutics.RAF1 扩增驱动了一部分膀胱癌,并使其对 MAPK 靶向治疗药物敏感。
J Clin Invest. 2021 Nov 15;131(22). doi: 10.1172/JCI147849.
8
IUPred3: prediction of protein disorder enhanced with unambiguous experimental annotation and visualization of evolutionary conservation.IUPred3:利用明确的实验注释和进化保守性可视化增强的蛋白质无序性预测。
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9
Critical assessment of protein intrinsic disorder prediction.蛋白质固有无序预测的关键评估。
Nat Methods. 2021 May;18(5):472-481. doi: 10.1038/s41592-021-01117-3. Epub 2021 Apr 19.
10
Mutations of Intrinsically Disordered Protein Regions Can Drive Cancer but Lack Therapeutic Strategies.内在无序蛋白区域的突变可引发癌症,但缺乏治疗策略。
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