Prediction of voltage-gated ion channel toxins by increment of diversity

Chaofeng Lan, Lei Zhang, Ming Zhu, Jingyu Wang, Ya Zhang
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Abstract

Voltage-gated ion channel is the molecular target for a broad range of toxins. Voltage-gated ion channel toxins are excellent pharmacological tools in toxicology and neuroscience. They have been used as molecular scaffolding agents, drugs, and insecticides. In this study, voltage-gated calcium, potassium and sodium channel toxins are predicted by the increment of diversity (ID) algorithm. Each protein is represented by 400 pseudo amino acid compositions and 9 MEME motif features. The Maximum Relevance Minimum Redundancy (MRMR) is applied for ranking 400 pseudo amino acid compositions. The results of jackknife test indicate that the best predictive results are obtained when using 50 higher ranked pseudo amino acid compositions and 9 MEME motif features. Based on the predictive results, our results suggest the usefulness and potential of ID algorithm for prediction of voltage-gated ion channel toxins using protein sequence derived information.
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利用多样性增量预测电压门控离子通道毒素
电压门控离子通道是多种毒素的分子靶点。电压门控离子通道毒素是毒理学和神经科学中很好的药理学工具。它们已被用作分子支架剂、药物和杀虫剂。本研究采用多样性增量(ID)算法对电压门控的钙、钾、钠通道毒素进行预测。每个蛋白由400个伪氨基酸组成和9个模因基序特征代表。应用最大相关最小冗余度(MRMR)对400种伪氨基酸组合进行排序。叠刀试验结果表明,利用50个排名靠前的伪氨基酸组合和9个模因基序特征可获得最佳的预测结果。基于预测结果,我们的研究结果表明ID算法利用蛋白质序列衍生信息预测电压门控离子通道毒素的有效性和潜力。
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