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IRESPred: Web Server for Prediction of Cellular and Viral Internal Ribosome Entry Site (IRES)

机译:IRESPRED:用于预测细胞和病毒内部核糖体入口部位(IRES)的Web服务器

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摘要

Cellular mRNAs are predominantly translated in a cap-dependent manner. However, some viral and a subset of cellular mRNAs initiate their translation in a cap-independent manner. This requires presence of a structured RNA element, known as, Internal Ribosome Entry Site (IRES) in their 5' untranslated regions (UTRs). Experimental demonstration of IRES in UTR remains a challenging task. Computational prediction of IRES merely based on sequence and structure conservation is also difficult, particularly for cellular IRES. A web server, IRESPred is developed for prediction of both viral and cellular IRES using Support Vector Machine (SVM). The predictive model was built using 35 features that are based on sequence and structural properties of UTRs and the probabilities of interactions between UTR and small subunit ribosomal proteins (SSRPs). The model was found to have 75.51% accuracy, 75.75% sensitivity, 75.25% specificity, 75.75% precision and Matthews Correlation Coefficient (MCC) of 0.51 in blind testing. IRESPred was found to perform better than the only available viral IRES prediction server, VIPS. The IRESPred server is freely available at http://bioinfo.net.in/IRESPred/.
机译:细胞mRNA主要以依赖性方式翻译。然而,一些病毒和蜂窝MRNA的子集以帽独立的方式引发它们的翻译。这需要在其5'未翻译区(UTRS)中存在的结构化RNA元素,称为内部核糖体入口位点(IRE)。 UTR中IRE的实验证明仍然是一个具有挑战性的任务。仅基于序列和结构守恒的IRES的计算预测也是困难的,特别是对于蜂窝室内的难度。使用支持向量机(SVM)开发了一种Web服务器,用于预测病毒和蜂窝IRE的预测。预测模型是使用基于UTR的序列和结构性质的35个特征构建的,以及UTR和小亚基核糖体蛋白(SSRP)之间的相互作用的概率。发现该模型具有75.51%的精度,灵敏度为75.75%,特异性75.25%,75.75%的精度,75.75%的精度和马太福德相关系数(MCC)为0.51的盲试验。发现IRESPRED比唯一可用的病毒IRES预测服务器,vips表现更好。 IRESPRED服务器在http://bioinfo.net.in/irespred/上自由使用。

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