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Classification and Analysis of Regulatory Pathways Using Graph Property, Biochemical and Physicochemical Property, and Functional Property

机译:利用图特性,生化特性,理化特性和功能特性对监管途径进行分类和分析

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摘要

Given a regulatory pathway system consisting of a set of proteins, can we predict which pathway class it belongs to? Such a problem is closely related to the biological function of the pathway in cells and hence is quite fundamental and essential in systems biology and proteomics. This is also an extremely difficult and challenging problem due to its complexity. To address this problem, a novel approach was developed that can be used to predict query pathways among the following six functional categories: (i) “Metabolism”, (ii) “Genetic Information Processing”, (iii) “Environmental Information Processing”, (iv) “Cellular Processes”, (v) “Organismal Systems”, and (vi) “Human Diseases”. The prediction method was established trough the following procedures: (i) according to the general form of pseudo amino acid composition (PseAAC), each of the pathways concerned is formulated as a 5570-D (dimensional) vector; (ii) each of components in the 5570-D vector was derived by a series of feature extractions from the pathway system according to its graphic property, biochemical and physicochemical property, as well as functional property; (iii) the minimum redundancy maximum relevance (mRMR) method was adopted to operate the prediction. A cross-validation by the jackknife test on a benchmark dataset consisting of 146 regulatory pathways indicated that an overall success rate of 78.8% was achieved by our method in identifying query pathways among the above six classes, indicating the outcome is quite promising and encouraging. To the best of our knowledge, the current study represents the first effort in attempting to identity the type of a pathway system or its biological function. It is anticipated that our report may stimulate a series of follow-up investigations in this new and challenging area.
机译:给定一个由一组蛋白质组成的调节途径系统,我们能否预测它属于哪个途径类别?这个问题与细胞中该途径的生物学功能密切相关,因此在系统生物学和蛋白质组学中是非常基本和必不可少的。由于其复杂性,这也是一个非常困难和具有挑战性的问题。为了解决这个问题,开发了一种新颖的方法,可用于预测以下六个功能类别之间的查询途径:(i)“代谢”,(ii)“遗传信息处理”,(iii)“环境信息处理”, (iv)“细胞过程”,(v)“有机系统”和(vi)“人类疾病”。通过以下程序建立了预测方法:(i)根据伪氨基酸组成(PseAAC)的一般形式,将有关的每种途径表述为5570-D(维)载体; (ii)5570-D载体中的每个成分均根据其图形特性,生化和物理化学特性以及功能特性,通过从通路系统进行一系列特征提取而得到; (iii)采用最小冗余最大相关性(mRMR)方法进行预测。通过对由146条调控途径组成的基准数据集进行的折刀检验的交叉验证表明,通过我们的方法来识别上述六类中的查询途径,该方法的总体成功率为78.8%,这表明结果是非常有希望和令人鼓舞的。据我们所知,当前的研究代表了试图鉴定通路系统的类型或其生物学功能的第一步。可以预料,我们的报告可能会刺激这一新的充满挑战的领域的一系列后续调查。

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