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首页> 外文期刊>Combinatorial chemistry & high throughput screening >Self-Organizing Map (SOM) and Support Vector Machine (SVM) Models for the Prediction of Human Epidermal Growth Factor Receptor (EGFR/ErbB-1) Inhibitors
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Self-Organizing Map (SOM) and Support Vector Machine (SVM) Models for the Prediction of Human Epidermal Growth Factor Receptor (EGFR/ErbB-1) Inhibitors

机译:自组织图(SOM)和支持向量机(SVM)模型用于预测人类表皮生长因子受体(EGFR / ErbB-1)抑制剂

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摘要

EGFR (ErbB-1/HER1) kinase plays an important role in cancer therapy. Two classification models were established to predict whether a compound is an inhibitor or a decoy of human EGFR (ErbR-1) by using Kohonen's self-organizing map (SOM) and support vector machine (SVM). A dataset containing 1248 ATP binding site inhibitors and 3090 decoys was collected and randomly divided into a training set (831 inhibitors and 2064 decoys) and a test set (417 inhibitors and 1029 decoys). The descriptors that represent molecular structures were calculated by software ADRIANA. Code. Thirteen significant descriptors including five global descriptors and eight 2D property autocorrelation descriptors were selected by Pearson correlation analysis and stepwise analysis. The prediction accuracies on training set and test set are 98.5% and 96.3% for SOM model, 99.0% and 97.0% for SVM model, respectively. Both of these two classification models have good performance on distinguishing EGFR inhibitors from decoys.
机译:EGFR(ErbB-1 / HER1)激酶在癌症治疗中起重要作用。通过使用Kohonen的自组织图(SOM)和支持向量机(SVM),建立了两个分类模型来预测化合物是人类EGFR(ErbR-1)的抑制剂还是诱饵。收集包含1248个ATP结合位点抑制剂和3090个诱饵的数据集,并将其随机分为训练集(831个抑制剂和2064个诱饵)和测试集(417个抑制剂和1029个诱饵)。代表分子结构的描述符由软件ADRIANA计算。码。通过Pearson相关分析和逐步分析,选择了13个重要的描述符,包括5个全局描述符和8个2D属性自相关描述符。对于SOM模型,训练集和测试集的预测准确度分别为98.5%和96.3%,对于SVM模型,分别为99.0%和97.0%。这两种分类模型在区分EGFR抑制剂和诱饵上均具有良好的性能。

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