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首页> 外文期刊>BMC Bioinformatics >Discover protein sequence signatures from protein-protein interaction data
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Discover protein sequence signatures from protein-protein interaction data

机译:从蛋白质间相互作用数据发现蛋白质序列特征

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Background The development of high-throughput technologies such as yeast two-hybrid systems and mass spectrometry technologies has made it possible to generate large protein-protein interaction (PPI) datasets. Mining these datasets for underlying biological knowledge has, however, remained a challenge. Results A total of 3108 sequence signatures were found, each of which was shared by a set of guest proteins interacting with one of 944 host proteins in Saccharomyces cerevisiae genome. Approximately 94% of these sequence signatures matched entries in InterPro member databases. We identified 84 distinct sequence signatures from the remaining 172 unknown signatures. The signature sharing information was then applied in predicting sub-cellular localization of yeast proteins and the novel signatures were used in identifying possible interacting sites. Conclusion We reported a method of PPI data mining that facilitated the discovery of novel sequence signatures using a large PPI dataset from S. cerevisiae genome as input. The fact that 94% of discovered signatures were known validated the ability of the approach to identify large numbers of signatures from PPI data. The significance of these discovered signatures was demonstrated by their application in predicting sub-cellular localizations and identifying potential interaction binding sites of yeast proteins.
机译:背景技术诸如酵母双杂交系统和质谱技术之类的高通量技术的发展使得产生大的蛋白质-蛋白质相互作用(PPI)数据集成为可能。然而,挖掘这些数据集以获取基础生物学知识仍然是一个挑战。结果共发现3108个序列特征,每个特征均由一组与啤酒酵母基因组中944个宿主蛋白相互作用的客体蛋白共享。这些序列签名中约有94%与InterPro成员数据库中的条目匹配。我们从剩余的172个未知特征中识别出84个不同的序列特征。然后将签名共享信息应用于预测酵母蛋白的亚细胞定位,并将新的签名用于识别可能的相互作用位点。结论我们报道了一种PPI数据挖掘方法,该方法使用来自酿酒酵母基因组的大型PPI数据集作为输入,有助于发现新的序列特征。 94%的发现签名是已知的事实证明了该方法从PPI数据中识别大量签名的能力。这些发现的特征的重要性通过其在预测亚细胞定位和鉴定酵母蛋白潜在的相互作用结合位点中的应用得到了证明。

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