• 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

IPs-GRUAtt:一种基于注意力机制的双向门控循环单元网络,用于预测新型冠状病毒感染的磷酸化位点

IPs-GRUAtt: An attention-based bidirectional gated recurrent unit network for predicting phosphorylation sites of SARS-CoV-2 infection.

作者信息

Zhang Guiyang, Tang Qiang, Feng Pengmian, Chen Wei

机构信息

State Key Laboratory of Southwestern Chinese Medicine Resources, Innovative Chengdu University of Traditional Chinese Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China.

State Key Laboratory of Southwestern Chinese Medicine Resources, School of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China.

出版信息

Mol Ther Nucleic Acids. 2023 Jun 13;32:28-35. doi: 10.1016/j.omtn.2023.02.027. Epub 2023 Feb 26.

DOI:10.1016/j.omtn.2023.02.027
PMID:36908648
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9968446/
Abstract

The global pandemic of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has generated tremendous concern and poses a serious threat to international public health. Phosphorylation is a common post-translational modification affecting many essential cellular processes and is inextricably linked to SARS-CoV-2 infection. Hence, accurate identification of phosphorylation sites will be helpful to understand the mechanisms of SARS-CoV-2 infection and mitigate the ongoing COVID-19 pandemic. In the present study, an attention-based bidirectional gated recurrent unit network, called IPs-GRUAtt, was proposed to identify phosphorylation sites in SARS-CoV-2-infected host cells. Comparative results demonstrated that IPs-GRUAtt surpassed both state-of-the-art machine-learning methods and existing models for identifying phosphorylation sites. Moreover, the attention mechanism made IPs-GRUAtt able to extract the key features from protein sequences. These results demonstrated that the IPs-GRUAtt is a powerful tool for identifying phosphorylation sites. For facilitating its academic use, a freely available online web server for IPs-GRUAtt is provided at http://cbcb.cdutcm.edu.cn/phosphory/.

摘要

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染的全球大流行引起了极大关注,并对国际公共卫生构成严重威胁。磷酸化是一种常见的翻译后修饰,影响许多重要的细胞过程,并且与SARS-CoV-2感染有着千丝万缕的联系。因此,准确识别磷酸化位点将有助于理解SARS-CoV-2感染的机制,并缓解当前的COVID-19大流行。在本研究中,提出了一种基于注意力的双向门控循环单元网络,称为IPs-GRUAtt,用于识别SARS-CoV-2感染的宿主细胞中的磷酸化位点。比较结果表明,IPs-GRUAtt超过了最先进的机器学习方法和现有的磷酸化位点识别模型。此外,注意力机制使IPs-GRUAtt能够从蛋白质序列中提取关键特征。这些结果表明,IPs-GRUAtt是识别磷酸化位点的有力工具。为便于其学术使用,在http://cbcb.cdutcm.edu.cn/phosphory/提供了一个免费的IPs-GRUAtt在线网络服务器。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d08/10025107/3c1d34108557/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d08/10025107/647a9720e913/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d08/10025107/f7dcfe96a30a/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d08/10025107/6df08f976077/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d08/10025107/b8554ce4bf09/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d08/10025107/b0078cf8f317/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d08/10025107/3c1d34108557/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d08/10025107/647a9720e913/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d08/10025107/f7dcfe96a30a/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d08/10025107/6df08f976077/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d08/10025107/b8554ce4bf09/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d08/10025107/b0078cf8f317/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d08/10025107/3c1d34108557/gr5.jpg

相似文献

1
IPs-GRUAtt: An attention-based bidirectional gated recurrent unit network for predicting phosphorylation sites of SARS-CoV-2 infection.IPs-GRUAtt:一种基于注意力机制的双向门控循环单元网络,用于预测新型冠状病毒感染的磷酸化位点
Mol Ther Nucleic Acids. 2023 Jun 13;32:28-35. doi: 10.1016/j.omtn.2023.02.027. Epub 2023 Feb 26.
2
Adaptive learning embedding features to improve the predictive performance of SARS-CoV-2 phosphorylation sites.自适应学习嵌入特征,以提高 SARS-CoV-2 磷酸化位点的预测性能。
Bioinformatics. 2023 Nov 1;39(11). doi: 10.1093/bioinformatics/btad627.
3
Advancing the accuracy of SARS-CoV-2 phosphorylation site detection via meta-learning approach.通过元学习方法提高 SARS-CoV-2 磷酸化位点检测的准确性。
Brief Bioinform. 2023 Nov 22;25(1). doi: 10.1093/bib/bbad433.
4
PhosBERT: A self-supervised learning model for identifying phosphorylation sites in SARS-CoV-2-infected human cells.PhosBERT:一种用于识别 SARS-CoV-2 感染人类细胞中磷酸化位点的自监督学习模型。
Methods. 2024 Oct;230:140-146. doi: 10.1016/j.ymeth.2024.08.004. Epub 2024 Aug 22.
5
DeepIPs: comprehensive assessment and computational identification of phosphorylation sites of SARS-CoV-2 infection using a deep learning-based approach.DeepIPs:基于深度学习的方法对 SARS-CoV-2 感染的磷酸化位点进行全面评估和计算识别。
Brief Bioinform. 2021 Nov 5;22(6). doi: 10.1093/bib/bbab244.
6
A deep bidirectional recurrent neural network for identification of SARS-CoV-2 from viral genome sequences.一种用于从病毒基因组序列中识别 SARS-CoV-2 的深度双向循环神经网络。
Math Biosci Eng. 2021 Oct 15;18(6):8933-8950. doi: 10.3934/mbe.2021440.
7
BSG/CD147 and ACE2 receptors facilitate SARS-CoV-2 infection of human iPS cell-derived kidney podocytes.BSG/CD147和ACE2受体促进严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染人诱导多能干细胞衍生的肾足细胞。
bioRxiv. 2021 Nov 17:2021.11.16.468893. doi: 10.1101/2021.11.16.468893.
8
DE-MHAIPs: Identification of SARS-CoV-2 phosphorylation sites based on differential evolution multi-feature learning and multi-head attention mechanism.基于差分进化多特征学习和多头注意力机制的 SARS-CoV-2 磷酸化位点鉴定。
Comput Biol Med. 2023 Jun;160:106935. doi: 10.1016/j.compbiomed.2023.106935. Epub 2023 Apr 14.
9
Open Modification Searching of SARS-CoV-2-Human Protein Interaction Data Reveals Novel Viral Modification Sites.开放修饰的 SARS-CoV-2-人体蛋白相互作用数据搜索揭示了新型病毒修饰位点。
Mol Cell Proteomics. 2022 Dec;21(12):100425. doi: 10.1016/j.mcpro.2022.100425. Epub 2022 Oct 12.
10
DeepKla: An attention mechanism-based deep neural network for protein lysine lactylation site prediction.DeepKla:一种基于注意力机制的用于蛋白质赖氨酸乳酰化位点预测的深度神经网络。
Imeta. 2022 Mar 15;1(1):e11. doi: 10.1002/imt2.11. eCollection 2022 Mar.

引用本文的文献

1
Empirical Comparison and Analysis of Artificial Intelligence-Based Methods for Identifying Phosphorylation Sites of SARS-CoV-2 Infection.基于人工智能的新冠病毒感染磷酸化位点识别方法的实证比较与分析
Int J Mol Sci. 2024 Dec 21;25(24):13674. doi: 10.3390/ijms252413674.
2
GBMPhos: A Gating Mechanism and Bi-GRU-Based Method for Identifying Phosphorylation Sites of SARS-CoV-2 Infection.GBMPhos:一种基于门控机制和双向门控循环单元的新冠病毒感染磷酸化位点识别方法。
Biology (Basel). 2024 Oct 6;13(10):798. doi: 10.3390/biology13100798.
3
H2Opred: a robust and efficient hybrid deep learning model for predicting 2'-O-methylation sites in human RNA.

本文引用的文献

1
Structural basis for SARS-CoV-2 nucleocapsid (N) protein recognition by 14-3-3 proteins.SARS-CoV-2 核衣壳(N)蛋白被 14-3-3 蛋白识别的结构基础。
J Struct Biol. 2022 Sep;214(3):107879. doi: 10.1016/j.jsb.2022.107879. Epub 2022 Jun 30.
2
Human phospho-signaling networks of SARS-CoV-2 infection are rewired by population genetic variants.人群遗传变异重塑 SARS-CoV-2 感染的人类磷酸化信号网络。
Mol Syst Biol. 2022 May;18(5):e10823. doi: 10.15252/msb.202110823.
3
SARS-CoV-2 Infection Triggers Phosphorylation: Potential Target for Anti-COVID-19 Therapeutics.
H2Opred:一种用于预测人 RNA 2'-O-甲基化位点的稳健高效的混合深度学习模型。
Brief Bioinform. 2023 Nov 22;25(1). doi: 10.1093/bib/bbad476.
4
Advancing the accuracy of SARS-CoV-2 phosphorylation site detection via meta-learning approach.通过元学习方法提高 SARS-CoV-2 磷酸化位点检测的准确性。
Brief Bioinform. 2023 Nov 22;25(1). doi: 10.1093/bib/bbad433.
5
m5U-GEPred: prediction of RNA 5-methyluridine sites based on sequence-derived and graph embedding features.m5U-GEPred:基于序列衍生特征和图嵌入特征预测RNA 5-甲基尿苷位点
Front Microbiol. 2023 Oct 23;14:1277099. doi: 10.3389/fmicb.2023.1277099. eCollection 2023.
SARS-CoV-2 感染触发磷酸化:抗 COVID-19 治疗的潜在靶点。
Front Immunol. 2022 Feb 17;13:829474. doi: 10.3389/fimmu.2022.829474. eCollection 2022.
4
Novel inhibitors to ADP ribose phosphatase of SARS-CoV-2 identified by structure-based high throughput virtual screening and molecular dynamics simulations.通过基于结构的高通量虚拟筛选和分子动力学模拟鉴定出的新型严重急性呼吸综合征冠状病毒2(SARS-CoV-2)ADP核糖磷酸酶抑制剂。
Comput Biol Med. 2022 Jan;140:105084. doi: 10.1016/j.compbiomed.2021.105084. Epub 2021 Nov 30.
5
DeepIPs: comprehensive assessment and computational identification of phosphorylation sites of SARS-CoV-2 infection using a deep learning-based approach.DeepIPs:基于深度学习的方法对 SARS-CoV-2 感染的磷酸化位点进行全面评估和计算识别。
Brief Bioinform. 2021 Nov 5;22(6). doi: 10.1093/bib/bbab244.
6
Multilevel proteomics reveals host perturbations by SARS-CoV-2 and SARS-CoV.多水平蛋白质组学揭示 SARS-CoV-2 和 SARS-CoV 对宿主的干扰。
Nature. 2021 Jun;594(7862):246-252. doi: 10.1038/s41586-021-03493-4. Epub 2021 Apr 12.
7
mRNALocater: Enhance the prediction accuracy of eukaryotic mRNA subcellular localization by using model fusion strategy.mRNA 定位器:通过模型融合策略提高真核 mRNA 亚细胞定位的预测准确性。
Mol Ther. 2021 Aug 4;29(8):2617-2623. doi: 10.1016/j.ymthe.2021.04.004. Epub 2021 Apr 3.
8
The Mechanism of SARS-CoV-2 Nucleocapsid Protein Recognition by the Human 14-3-3 Proteins.SARS-CoV-2 核衣壳蛋白被人 14-3-3 蛋白识别的机制。
J Mol Biol. 2021 Apr 16;433(8):166875. doi: 10.1016/j.jmb.2021.166875. Epub 2021 Feb 5.
9
Growth Factor Receptor Signaling Inhibition Prevents SARS-CoV-2 Replication.生长因子受体信号抑制可预防 SARS-CoV-2 复制。
Mol Cell. 2020 Oct 1;80(1):164-174.e4. doi: 10.1016/j.molcel.2020.08.006. Epub 2020 Aug 11.
10
The Landscape of Human Cancer Proteins Targeted by SARS-CoV-2.人类癌症蛋白被 SARS-CoV-2 靶向的全景图。
Cancer Discov. 2020 Jul;10(7):916-921. doi: 10.1158/2159-8290.CD-20-0559. Epub 2020 May 22.