Species-specific model based on sequence and structural information for ubiquitination sites prediction

IF 4.7 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Molecular Biology Pub Date : 2024-09-07 DOI:10.1016/j.jmb.2024.168781
Weimin Li , Nan Chen , Jie Wang , Yin Luo , Huazhong Liu , Jihong Ding , Qun Jin
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Abstract

Ubiquitination is a common post-translational modification of proteins in eukaryotic cells, and it is also a significant method of regulating protein biological function. Computational methods for predicting ubiquitination sites can serve as a cost-effective and time-saving alternative to experimental methods. Existing computational methods often build classifiers based on protein sequence information, physical and chemical properties of amino acids, evolutionary information, and structural parameters. However, structural information about most proteins cannot be found in existing databases directly. The features of proteins differ among species, and some species have small amounts of ubiquitinated proteins. Therefore, it is necessary to develop species-specific models that can be applied to datasets with small sample sizes. To solve these problems, we propose a species-specific model (SSUbi) based on a capsule network, which integrates proteins’ sequence and structural information. In this model, the feature extraction module is composed of two sub-modules that extract multi-dimensional features from sequence and structural information respectively. In the submodule, the convolution operation is used to extract encoding dimension features, and the channel attention mechanism is used to extract feature map dimension features. After integrating the multi-dimensional features from both types of information, the species-specific capsule network further converts the features into capsule vectors and classifies species-specific ubiquitination sites. The experimental results show that SSUbi can effectively improve the prediction performance of species with small sample sizes and outperform other models.

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基于序列和结构信息的泛素化位点预测物种特异性模型。
泛素化是真核细胞中常见的蛋白质翻译后修饰,也是调节蛋白质生物功能的重要方法。使用计算方法预测泛素化位点可以取代昂贵而耗时的实验方法。现有的计算方法通常根据蛋白质序列信息、氨基酸的物理和化学特性、进化信息和结构参数建立分类器。然而,大多数蛋白质的结构信息无法直接从现有数据库中找到。不同物种的蛋白质特征各不相同,有些物种的泛素化蛋白质数量较少。因此,有必要开发可应用于样本量较小的数据集的物种特异性模型。为了解决这些问题,我们提出了一种基于胶囊网络的物种特异性模型(SSUbi),它整合了蛋白质的序列和结构信息。在该模型中,特征提取模块由两个子模块组成,分别从序列和结构信息中提取多维特征。在子模块中,利用卷积运算提取编码维度特征,利用通道注意机制提取特征图维度特征。整合两种信息的多维特征后,物种特异性胶囊网络进一步将特征转换为胶囊向量,并对物种特异性泛素化位点进行分类。实验结果表明,SSUbi 能有效提高小样本量物种的预测性能,并优于其他模型。
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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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Editorial Board Outside Front Cover Assembly of the human multi-tRNA synthetase complex through leucine zipper motifs. Corrigendum to “The Role of ATG9 Vesicles in Autophagosome Biogenesis” [J. Mol. Biol. 436(15) (2024) 168489] Structural studies on Mycobacterial NudC reveal a class of zinc independent NADH pyrophosphatase.
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