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CIPPN: computational identification of protein pupylation sites by using neural network

机译:CIPPN:使用神经网络通过计算机识别蛋白的酰化位点

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摘要

Recently, experiments revealed the pupylation to be a signal for the selective regulation of proteins in several serious human diseases. As one of the most significant post translational modification in the field of biology and disease, pupylation has the ability to playing the key role in the regulation various diseases’ biological processes. Meanwhile, effectively identification such type modification will be helpful for proteins to perform their biological functions and contribute to understanding the molecular mechanism, which is the foundation of drug design. The existing algorithms of identification such types of modified sites often have some defects, such as low accuracy and time-consuming. In this research, the pupylation sites’ identification model, CIPPN, demonstrates better performance than other existing approaches in this field. The proposed predictor achieves Acc value of 89.12 and Mcc value of 0.7949 in 10-fold cross-validation tests in the Pupdb Database (). Significantly, such algorithm not only investigates the sequential, structural and evolutionary hallmarks around pupylation sites but also compares the differences of pupylation from the environmental, conservative and functional characterization of substrates. Therefore, the proposed feature description approach and algorithm results prove to be useful for further experimental investigation of such modification’s identification.
机译:最近,实验表明,Pupylation是选择性调节几种严重人类疾病中蛋白质的信号。 pupylation是生物学和疾病领域最重要的翻译后修饰之一,具有在调节各种疾病的生物学过程中发挥关键作用的能力。同时,有效识别这种类型修饰将有助于蛋白质发挥其生物学功能,有助于理解分子机制,这是药物设计的基础。识别这种类型的修饰位点的现有算法通常具有一些缺陷,例如准确性低和费时。在这项研究中,联合化位点的识别模型CIPPN展示了比该领域其他现有方法更好的性能。在Pupdb数据库()中进行10倍交叉验证测试后,拟议的预测变量实现了89.12的Acc值和0.7949的Mcc值。值得注意的是,这种算法不仅研究了Pupylation位点周围的顺序,结构和进化特征,而且还比较了Pupylation与底物的环境特征,保守特征和功能特征之间的差异。因此,所提出的特征描述方法和算法结果被证明可用于对这种修改的识别进行进一步的实验研究。

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