首页> 外文期刊>Frontiers in Bioengineering and Biotechnology >Identifying Acetylation Protein by fusing its PseAAC and Functional Domain Annotation Running Title: Identifying Acetylation Protein
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Identifying Acetylation Protein by fusing its PseAAC and Functional Domain Annotation Running Title: Identifying Acetylation Protein

机译:通过融合PseAAC和功能域注释来鉴定乙酰化蛋白标题:乙酰化蛋白的鉴定

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摘要

Acetylation is one of post-translational modification (PTM), which is a reaction, usually with acetic acid, that introduces an acetyl radical into an organic compound. To understand the mechanism of acetylation profoundly, it is necessary to identify acetylation protein correctly in biological systems. Although high throughput experimental studies using mass spectrometry have identified many acetylation sites, the vast majority of acetylation sites remain undiscovered, even in well studied systems. To reduce experiment cost and improve the effectiveness and efficiency of acetylation site identification, computational (in silico) methods have been introduced and developed based on informatics techniques. In fact, if there is an approach can predict whether a query protein may be acetylated or may not, it is no doubt a very meaningful and effective method for this issue. In this study, we developed a novel computational method for predicting acetylation proteins by extracting features from sequence conservation information via grey system model and KNN scores based on functional domain annotation (FDA) and subcellular localization information. Together with the detailed features analysis and application of Relief feature selection algorithm, the paper also showed the results of 5-fold cross-validation on three datasets. The achieved accuracies are all satisfactory, as the mean performance, the accuracy is 77.10%, the Matthew’s correlation coefficient is 0.5457, and the AUC value is 0.8389. These works might guide the related experimental validation and provide useful insights for studying the mechanisms of acetylation, and the proposed method is looking forward to give a powerful help for further studies of other PTM process. Furthermore, a user-friendly web-server for “iACetyP” has been established, and is accessible at http://www.jci-bioinfo.cn/iAcetyP.
机译:乙酰化是翻译后修饰(PTM)之一,通常是与乙酸反应,将乙酰基引入有机化合物中。为了深刻理解乙酰化的机理,有必要在生物系统中正确鉴定乙酰化蛋白。尽管使用质谱的高通量实验研究已经确定了许多乙酰化位点,但即使在经过充分研究的系统中,绝大多数乙酰化位点仍未被发现。为了降低实验成本并提高乙酰化位点识别的效率和效率,已经基于信息技术引入和开发了计算机方法(计算机)。实际上,如果有一种方法可以预测查询蛋白是否会被乙酰化,那么毫无疑问,这是一种非常有意义和有效的方法。在这项研究中,我们开发了一种新的预测乙酰化蛋白的计算方法,该方法通过基于功能域注释(FDA)和亚细胞定位信息的灰色系统模型和KNN分数从序列保守性信息中提取特征。结合详细的特征分析和救济特征选择算法的应用,本文还显示了对三个数据集进行5倍交叉验证的结果。达到的精度都令人满意,平均性能为77.10%,马修相关系数为0.5457,AUC值为0.8389。这些工作可能会指导相关的实验验证,并为研究乙酰化的机理提供有用的见识,并且所提出的方法有望为进一步研究其他PTM工艺提供有力的帮助。此外,已经建立了一个用于“ iACetyP”的用户友好的Web服务器,可以从http://www.jci-bioinfo.cn/iAcetyP进行访问。

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