• 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

OpenProt 2021:深入注释真核生物基因组的编码潜能。

OpenProt 2021: deeper functional annotation of the coding potential of eukaryotic genomes.

机构信息

Department of Biochemistry and Functional Genomics, Université de Sherbrooke, 3201 Jean Mignault, Sherbrooke, QC J1E 4K8, Canada.

PROTEO, Quebec Network for Research on Protein Function, Structure, and Engineering, Université Laval, Quebec City, QC G1V0A6, Canada.

出版信息

Nucleic Acids Res. 2021 Jan 8;49(D1):D380-D388. doi: 10.1093/nar/gkaa1036.

DOI:10.1093/nar/gkaa1036
PMID:33179748
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7779043/
Abstract

OpenProt (www.openprot.org) is the first proteogenomic resource supporting a polycistronic annotation model for eukaryotic genomes. It provides a deeper annotation of open reading frames (ORFs) while mining experimental data for supporting evidence using cutting-edge algorithms. This update presents the major improvements since the initial release of OpenProt. All species support recent NCBI RefSeq and Ensembl annotations, with changes in annotations being reported in OpenProt. Using the 131 ribosome profiling datasets re-analysed by OpenProt to date, non-AUG initiation starts are reported alongside a confidence score of the initiating codon. From the 177 mass spectrometry datasets re-analysed by OpenProt to date, the unicity of the detected peptides is controlled at each implementation. Furthermore, to guide the users, detectability statistics and protein relationships (isoforms) are now reported for each protein. Finally, to foster access to deeper ORF annotation independently of one's bioinformatics skills or computational resources, OpenProt now offers a data analysis platform. Users can submit their dataset for analysis and receive the results from the analysis by OpenProt. All data on OpenProt are freely available and downloadable for each species, the release-based format ensuring a continuous access to the data. Thus, OpenProt enables a more comprehensive annotation of eukaryotic genomes and fosters functional proteomic discoveries.

摘要

OpenProt(www.openprot.org)是第一个支持真核生物基因组多顺反子注释模型的蛋白质组学资源。它通过使用最先进的算法挖掘实验数据来提供更深入的开放阅读框(ORF)注释,并为支持证据提供了更深入的注释。此更新介绍了自 OpenProt 初始发布以来的主要改进。所有物种都支持最新的 NCBI RefSeq 和 Ensembl 注释,OpenProt 会报告注释的更改。使用 OpenProt 迄今为止重新分析的 131 个核糖体分析数据集,报告了非 AUG 起始的起始密码子及其起始密码子置信度评分。从 OpenProt 迄今为止重新分析的 177 个质谱数据集,在每个实现中都控制了检测到的肽的唯一性。此外,为了指导用户,现在为每个蛋白质报告了可检测性统计信息和蛋白质关系(同工型)。最后,为了促进在不依赖于用户生物信息学技能或计算资源的情况下访问更深入的 ORF 注释,OpenProt 现在提供了一个数据分析平台。用户可以提交他们的数据集进行分析,并从 OpenProt 接收分析结果。OpenProt 上的所有数据都可免费获得,并且可以下载每个物种的数据,基于版本的格式确保了对数据的持续访问。因此,OpenProt 能够更全面地注释真核生物基因组,并促进功能蛋白质组学的发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336f/7779043/ad1d87e3497f/gkaa1036fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336f/7779043/557eed14d3ac/gkaa1036fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336f/7779043/ad1d87e3497f/gkaa1036fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336f/7779043/557eed14d3ac/gkaa1036fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336f/7779043/ad1d87e3497f/gkaa1036fig2.jpg

相似文献

1
OpenProt 2021: deeper functional annotation of the coding potential of eukaryotic genomes.OpenProt 2021:深入注释真核生物基因组的编码潜能。
Nucleic Acids Res. 2021 Jan 8;49(D1):D380-D388. doi: 10.1093/nar/gkaa1036.
2
OpenProt: a more comprehensive guide to explore eukaryotic coding potential and proteomes.OpenProt:探索真核生物编码潜能和蛋白质组的更全面指南。
Nucleic Acids Res. 2019 Jan 8;47(D1):D403-D410. doi: 10.1093/nar/gky936.
3
How to Illuminate the Dark Proteome Using the Multi-omic OpenProt Resource.如何利用多组学开放蛋白质组资源照亮暗蛋白质组。
Curr Protoc Bioinformatics. 2020 Sep;71(1):e103. doi: 10.1002/cpbi.103.
4
Mass Spectrometry-Based Proteomics Analyses Using the OpenProt Database to Unveil Novel Proteins Translated from Non-Canonical Open Reading Frames.基于质谱的蛋白质组学分析,利用OpenProt数据库揭示从非经典开放阅读框翻译而来的新型蛋白质。
J Vis Exp. 2019 Apr 11(146). doi: 10.3791/59589.
5
Exploring the Alternative Proteome with OpenProt and Mass Spectrometry.探索开放蛋白质组学和质谱技术中的替代蛋白质组。
Methods Mol Biol. 2024;2836:3-17. doi: 10.1007/978-1-0716-4007-4_1.
6
OpenProt 2.0 builds a path to the functional characterization of alternative proteins.OpenProt 2.0 为探索替代蛋白的功能特性开辟了道路。
Nucleic Acids Res. 2024 Jan 5;52(D1):D522-D528. doi: 10.1093/nar/gkad1050.
7
Peptimapper: proteogenomics workflow for the expert annotation of eukaryotic genomes.Peptimapper:用于真核生物基因组专家注释的蛋白质基因组学工作流程。
BMC Genomics. 2019 Jan 17;20(1):56. doi: 10.1186/s12864-019-5431-9.
8
smORFer: a modular algorithm to detect small ORFs in prokaryotes.smORFer:一种用于在原核生物中检测小开放阅读框的模块化算法。
Nucleic Acids Res. 2021 Sep 7;49(15):e89. doi: 10.1093/nar/gkab477.
9
Comparison of RefSeq protein-coding regions in human and vertebrate genomes.比较人类和脊椎动物基因组中的 RefSeq 编码蛋白区域。
BMC Genomics. 2013 Sep 25;14:654. doi: 10.1186/1471-2164-14-654.
10
An integrative strategy to identify the entire protein coding potential of prokaryotic genomes by proteogenomics.通过蛋白质基因组学鉴定原核基因组全部蛋白质编码潜能的综合策略。
Genome Res. 2017 Dec;27(12):2083-2095. doi: 10.1101/gr.218255.116. Epub 2017 Nov 15.

引用本文的文献

1
Identification of Small Open Reading Frame-Encoded Peptides in Glioma by an Optimized Proteomics Strategy.通过优化的蛋白质组学策略鉴定胶质瘤中小开放阅读框编码的肽段
Mol Cell Proteomics. 2025 Jun 11;24(7):101016. doi: 10.1016/j.mcpro.2025.101016.
2
Harnessing Noncanonical Proteins for Next-Generation Drug Discovery and Diagnosis.利用非规范蛋白质进行下一代药物发现与诊断。
WIREs Mech Dis. 2025 May-Jun;17(3):e70001. doi: 10.1002/wsbm.70001.
3
Current Perspectives on Functional Involvement of Micropeptides in Virus-Host Interactions.

本文引用的文献

1
Factorial study of the RNA-seq computational workflow identifies biases as technical gene signatures.RNA测序计算工作流程的析因研究将偏差识别为技术基因特征。
NAR Genom Bioinform. 2020 Jun 29;2(2):lqaa043. doi: 10.1093/nargab/lqaa043. eCollection 2020 Jun.
2
The FUS gene is dual-coding with both proteins contributing to FUS-mediated toxicity.FUS 基因具有双重编码功能,两种蛋白质都有助于 FUS 介导的毒性。
EMBO Rep. 2021 Jan 7;22(1):e50640. doi: 10.15252/embr.202050640. Epub 2020 Nov 23.
3
Identification and analysis of small proteins and short open reading frame encoded peptides in Hep3B cell.
微小肽在病毒-宿主相互作用中功能参与的当前观点
Int J Mol Sci. 2025 Apr 12;26(8):3651. doi: 10.3390/ijms26083651.
4
Proteomics-based characterization of ribosome heterogeneity in adult mouse organs.基于蛋白质组学对成年小鼠器官中核糖体异质性的表征
Cell Mol Life Sci. 2025 Apr 24;82(1):175. doi: 10.1007/s00018-025-05708-7.
5
Small open reading frame-encoded microproteins in cancer: identification, biological functions and clinical significance.癌症中的小开放阅读框编码微蛋白:鉴定、生物学功能及临床意义
Mol Cancer. 2025 Apr 2;24(1):105. doi: 10.1186/s12943-025-02278-x.
6
Enhanced Discovery of Alternative Proteins (AltProts) in Mouse Cardiac Development Using Data-Independent Acquisition (DIA) Proteomics.利用数据非依赖采集(DIA)蛋白质组学增强小鼠心脏发育过程中替代蛋白(AltProts)的发现
Anal Chem. 2025 Jan 28;97(3):1517-1527. doi: 10.1021/acs.analchem.4c02924. Epub 2025 Jan 15.
7
Mass Spectrometry-Based Workflow for the Identification and Quantification of Alternative and Canonical Proteins in Pancreatic Cancer Cells.基于质谱的流程用于鉴定和定量胰腺癌细胞中的可变蛋白和典型蛋白
Cells. 2024 Nov 28;13(23):1966. doi: 10.3390/cells13231966.
8
RiboSeq.Org: an integrated suite of resources for ribosome profiling data analysis and visualization.RiboSeq.Org:用于核糖体谱数据分析与可视化的综合资源套件。
Nucleic Acids Res. 2025 Jan 6;53(D1):D268-D274. doi: 10.1093/nar/gkae1020.
9
Proteomics Can Rise to the Challenge of Pseudogenes' Coding Nature.蛋白质组学能够应对假基因编码特性带来的挑战。
J Proteome Res. 2024 Dec 6;23(12):5233-5249. doi: 10.1021/acs.jproteome.4c00116. Epub 2024 Nov 1.
10
Alternative transcripts recode human genes to express overlapping, frameshifted microproteins.可变转录本对人类基因进行重新编码,以表达重叠的、移码的微小蛋白质。
bioRxiv. 2024 Oct 25:2024.10.22.619581. doi: 10.1101/2024.10.22.619581.
鉴定和分析 Hep3B 细胞中的小蛋白和短开放阅读框编码肽。
J Proteomics. 2021 Jan 6;230:103965. doi: 10.1016/j.jprot.2020.103965. Epub 2020 Sep 3.
4
How to Illuminate the Dark Proteome Using the Multi-omic OpenProt Resource.如何利用多组学开放蛋白质组资源照亮暗蛋白质组。
Curr Protoc Bioinformatics. 2020 Sep;71(1):e103. doi: 10.1002/cpbi.103.
5
Comparative Proteomic Profiling of Unannotated Microproteins and Alternative Proteins in Human Cell Lines.人类细胞系中未注释的微蛋白和替代蛋白的比较蛋白质组学分析。
J Proteome Res. 2020 Aug 7;19(8):3418-3426. doi: 10.1021/acs.jproteome.0c00254. Epub 2020 Jun 3.
6
Reconsidering proteomic diversity with functional investigation of small ORFs and alternative ORFs.重新考虑小 ORF 和替代 ORF 的功能研究中的蛋白质组多样性。
Exp Cell Res. 2020 Aug 1;393(1):112057. doi: 10.1016/j.yexcr.2020.112057. Epub 2020 May 6.
7
Reference and Ghost Proteins Identification in Rat C6 Glioma Extracellular Vesicles.大鼠C6胶质瘤细胞外囊泡中参考蛋白和“幽灵”蛋白的鉴定
iScience. 2020 May 22;23(5):101045. doi: 10.1016/j.isci.2020.101045. Epub 2020 Apr 10.
8
Alternative proteins are functional regulators in cell reprogramming by PKA activation.替代蛋白通过 PKA 激活成为细胞重编程的功能调节剂。
Nucleic Acids Res. 2020 Aug 20;48(14):7864-7882. doi: 10.1093/nar/gkaa277.
9
The microproteome of cancer: From invisibility to relevance.癌症的微蛋白质组学:从不可见性到相关性。
Exp Cell Res. 2020 Jul 1;392(1):111997. doi: 10.1016/j.yexcr.2020.111997. Epub 2020 Apr 14.
10
Ribosome profiling at isoform level reveals evolutionary conserved impacts of differential splicing on the proteome.核糖体图谱分析在异构体水平上揭示了可变剪接对蛋白质组的进化保守影响。
Nat Commun. 2020 Apr 14;11(1):1768. doi: 10.1038/s41467-020-15634-w.