首页> 外文会议>Brazilian Symposium on Bioinformatics(BSB 2005); 20050727-29; Sao Leopoldo(BR) >Prediction of Myotoxic and Neurotoxic Activities in Phospholipases A2 from Primary Sequence Analysis
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Prediction of Myotoxic and Neurotoxic Activities in Phospholipases A2 from Primary Sequence Analysis

机译:从一级序列分析预测磷脂酶A2的肌毒性和神经毒性活性。

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We developed a methodology to predict myotoxicity and neurotoxicity of proteins of the family of Phospholipases A2 (PLA2) from sequence data. Combining two bioinformatics tools, MEME and HMMER, it was possible to detect conserved motifs and represent them as Hidden Markov Models (HMMs). In ten-fold cross validation testing we have determined the efficacy of each motif on prediction of PLA2 function. We selected motifs whose efficacy in predict function were above 60% at the Minimum Error Point (MEP), the score in which there are fewest both false positives and false negatives. Combining HMMs of the best motifs for each function, we have achieved a mean efficacy of 98 ± 4% on prediction of myotoxic function and 77.4 ± 4.8% on prediction of neurotoxicity. We have used the results of this work to build a web tool (available at www.cbiot.ufrgs.br/bioinfo/ phospholipase) to classify PLA2s of unknown function regarding myotoxic or neurotoxic activity.
机译:我们开发了一种方法,可以从序列数据中预测磷脂酶A2(PLA2)家族蛋白的肌毒性和神经毒性。结合MEME和HMMER这两种生物信息学工具,可以检测保守的基序并将其表示为隐马尔可夫模型(HMM)。在十项交叉验证测试中,我们确定了每个基序对PLA2功能预测的功效。我们选择了在最小错误点(MEP)上预测功能功效高于60%的模体,在该分数中,假阳性和假阴性最少。结合每种功能的最佳基序的HMM,我们在预测肌毒性功能方面的平均功效为98±4%,在预测神经毒性方面的平均功效为77.4±4.8%。我们已经使用这项工作的结果构建了一个网络工具(可从www.cbiot.ufrgs.br/bioinfo/phospholipase获得)对涉及肌毒性或神经毒性活性的功能未知的PLA2s进行分类。

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