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I-Mutant2.0: predicting stability changes upon mutation from the protein sequence or structure

机译:I-Mutant2.0:预测蛋白质序列或结构突变后的稳定性变化

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摘要

I-Mutant2.0 is a support vector machine (SVM)-based tool for the automatic prediction of protein stability changes upon single point mutations. I-Mutant2.0 predictions are performed starting either from the protein structure or, more importantly, from the protein sequence. This latter task, to the best of our knowledge, is exploited for the first time. The method was trained and tested on a data set derived from ProTherm, which is presently the most comprehensive available database of thermodynamic experimental data of free energy changes of protein stability upon mutation under different conditions. I-Mutant2.0 can be used both as a classifier for predicting the sign of the protein stability change upon mutation and as a regression estimator for predicting the related ΔΔG values. Acting as a classifier, I-Mutant2.0 correctly predicts (with a cross-validation procedure) 80% or 77% of the data set, depending on the usage of structural or sequence information, respectively. When predicting ΔΔG values associated with mutations, the correlation of predicted with expected/experimental values is 0.71 (with a standard error of 1.30 kcal/mol) and 0.62 (with a standard error of 1.45 kcal/mol) when structural or sequence information are respectively adopted. Our web interface allows the selection of a predictive mode that depends on the availability of the protein structure and/or sequence. In this latter case, the web server requires only pasting of a protein sequence in a raw format. We therefore introduce I-Mutant2.0 as a unique and valuable helper for protein design, even when the protein structure is not yet known with atomic resolution. Availability: .
机译:I-Mutant2.0是基于支持向量机(SVM)的工具,用于在单点突变时自动预测蛋白质稳定性的变化。从蛋白质结构或更重要的是从蛋白质序列开始进行I-Mutant2.0预测。就我们所知,后一项任务是第一次被利用。在ProTherm衍生的数据集上对该方法进行了培训和测试,ProTherm是目前最全面的热力学实验数据数据库,可在不同条件下突变后稳定蛋白质的自由能。 I-Mutant2.0既可以用作预测突变后蛋白质稳定性变化迹象的分类器,也可以用作预测相关ΔΔG值的回归估计器。作为分类器,I-Mutant2.0可以正确预测(使用交叉验证程序)数据集的80%或77%,这分别取决于结构或序列信息的用法。当预测与突变相关的ΔΔG值时,当结构或序列信息分别为时,预测值与预期/实验值的相关性分别为0.71(标准误差为1.30 kcal / mol)和0.62(标准误差为1.45 kcal / mol)。通过。我们的Web界面允许根据蛋白质结构和/或序列的可用性选择预测模式。在后一种情况下,Web服务器仅需要粘贴原始格式的蛋白质序列。因此,即使尚未以原子分辨率了解蛋白质结构,我们也将I-Mutant2.0作为蛋白质设计的独特而有价值的助手。可用性: 。

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