BEAGLE 2.0:利用形状导向RNA结构测定的RNA二级结构相似性检测的Web服务器。

IF 4.7 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
F. Ballesio , A. Teofani , C. Carrino , M. Catalano , M.L. Nicolaeasa , G. Ausiello , M. Helmer-Citterich , P.F. Gherardini
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引用次数: 0

摘要

近年来的研究强调了RNA二级结构在各种生物和病理过程中的重要作用。结构保守性可以揭示单靠序列分析无法检测到的同源性,这使得准确预测和比较RNA二级结构至关重要。BEAGLE算法通过动态规划实现RNA二级结构的成对比对,利用BEAR编码表示RNA二级结构。最初,BEAGLE被设计用于对用户提供的rna或有限数量的数据集进行成对比对。我们现在介绍BEAGLE 2.0,这是一个web服务器,旨在方便搜索用户提供的RNA分子和扩展的RNA二级结构数据集之间的结构相似性。这些数据集包括来自智人、小家鼠、丹尼奥雷奥、大肠杆菌、枯草芽孢杆菌和各种病毒(包括SARS-CoV-2)的SHAPE实验的结构。它还结合了来自NONCODE数据库的预测结构,用于广泛的动物和植物,以及基于Rfam家族中保守位置的约束的结构数据集。用户可以输入RNA序列或序列和二级结构的组合,使用点括号或BEAR格式。BEAGLE 2.0输出具有结构相似性和统计显著性的成对比对。此外,它还提供了二级结构的视觉表现,结构元素以不同的颜色突出显示。总的来说,BEAGLE 2.0可以利用实验支持的数据在RNA结构数据集中进行搜索,以识别感兴趣的RNA的结构相似性。BEAGLE 2.0可从https://beagle2.bio.uniroma2.it获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
BEAGLE 2.0: A Web Server for RNA Secondary Structure Similarity Detection Leveraging SHAPE-directed RNA Structure Determination
Recent studies underscore the significant role of RNA secondary structures in various biological and pathological processes. Structural conservation can reveal homologies undetectable by sequence analysis alone, making accurate prediction and comparison of RNA secondary structures crucial. The BEAGLE algorithm enables pairwise alignments of RNA secondary structures through dynamic programming, leveraging the BEAR encoding for RNA secondary structures representation. Initially, BEAGLE was designed to perform pairwise alignments of user-provided RNAs or against a limited number of datasets. We now introduce BEAGLE 2.0, a web server designed to facilitate the search for structural similarities between user-provided RNA molecules and an expanded collection of RNA secondary structure datasets. These datasets include structures derived from SHAPE experiments in Homo sapiens, Mus musculus, Danio rerio, Escherichia coli, Bacillus subtilis, and various viruses, including SARS-CoV-2. It also incorporates predicted structures from the NONCODE database for a wide range of animals and plants, as well as a dataset of structures based on constraints derived from conserved positions within the families present in Rfam. Users can input RNA sequences or a combination of sequences and secondary structures in either dot-bracket or BEAR format. BEAGLE 2.0 outputs pairwise alignments with measures of structural similarity and statistical significance. Additionally, it offers a visual representation of the secondary structures, with structural elements highlighted in different colors. Overall, BEAGLE 2.0 enables searches in RNA structure datasets leveraging experimentally supported data, to identify structural similarities in RNAs of interest. BEAGLE 2.0 is available at https://beagle2.bio.uniroma2.it.
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来源期刊
Journal of Molecular Biology
Journal of Molecular Biology 生物-生化与分子生物学
CiteScore
11.30
自引率
1.80%
发文量
412
审稿时长
28 days
期刊介绍: Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions. Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.
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