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分析和共识目前可用的内在蛋白无序注释源在 MobiDB 数据库中。

Analysis and consensus of currently available intrinsic protein disorder annotation sources in the MobiDB database.

机构信息

Department of Biology, University of Padova, Viale G. Colombo 3, 35131 Padova, Italy.

出版信息

BMC Bioinformatics. 2013;14 Suppl 7(Suppl 7):S3. doi: 10.1186/1471-2105-14-S7-S3. Epub 2013 Apr 22.

Abstract

BACKGROUND

Intrinsic protein disorder is becoming an increasingly important topic in protein science. During the last few years, intrinsically disordered proteins (IDPs) have been shown to play a role in many important biological processes, e.g. protein signalling and regulation. This has sparked a need to better understand and characterize different types of IDPs, their functions and roles. Our recently published database, MobiDB, provides a centralized resource for accessing and analysing intrinsic protein disorder annotations.

RESULTS

Here, we present a thorough description and analysis of the data made available by MobiDB, providing descriptive statistics on the various available annotation sources. Version 1.2.1 of the database contains annotations for ca. 4,500,000 UniProt sequences, covering all eukaryotic proteomes. In addition, we describe a novel consensus annotation calculation and its related weighting scheme. The comparison between disorder information sources highlights how the MobiDB consensus captures the main features of intrinsic disorder and correlates well with manually curated datasets. Finally, we demonstrate the annotation of 13 eukaryotic model organisms through MobiDB's datasets, and of an example protein through the interactive user interface.

CONCLUSIONS

MobiDB is a central resource for intrinsic disorder research, containing both experimental data and predictions. In the future it will be expanded to include additional information for all known proteins.

摘要

背景

蛋白质的固有无序性正成为蛋白质科学中一个日益重要的课题。在过去的几年中,无序蛋白质(IDP)已被证明在许多重要的生物过程中发挥作用,例如蛋白质信号转导和调控。这就需要更好地理解和描述不同类型的 IDP、它们的功能和作用。我们最近发布的数据库 MobiDB 为访问和分析固有蛋白质无序注释提供了一个集中的资源。

结果

在这里,我们对 MobiDB 提供的数据进行了全面的描述和分析,提供了各种可用注释源的描述性统计信息。数据库的 1.2.1 版本包含了大约 450 万个 UniProt 序列的注释,涵盖了所有真核生物的蛋白质组。此外,我们还描述了一种新的共识注释计算及其相关权重方案。无序信息源之间的比较突出了 MobiDB 共识如何捕获固有无序的主要特征,并与人工整理的数据集很好地相关。最后,我们通过 MobiDB 的数据集展示了 13 种真核模式生物的注释,以及通过交互式用户界面展示了一个示例蛋白质的注释。

结论

MobiDB 是固有无序研究的中心资源,包含实验数据和预测。在未来,它将扩展到包括所有已知蛋白质的其他信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5896/3633070/e02daee9acfd/1471-2105-14-S7-S3-1.jpg

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