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Large Scale Statistical Prediction of Protein-Protein Interaction by Potentially Interacting Domain (PID) Pair

机译:潜在的相互作用域(PID)对大规模统计蛋白质 - 蛋白质相互作用预测

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Protein-protein interaction plays a critical role in biological processes. The identification of interacting proteins by computational methods can provide new leads in functional studies of uncharacterized proteins without performing extensive experiments. We developed a database for the potentially interacting domain pairs (PID) extracted from a dataset of experimentally identified interacting protein pairs (DIP: database of interacting proteins) with InterPro, an integrated database of protein families, domains and functional sites. In developing protein interaction databases and predictive methods, sensitive statistical scoring systems is critical to provide a reliability index for accurate functional analysis of interaction networks. We presenta statistical scoring system, named "PID matrix score" as a measure of the interaction probability (interactability) between domains. This system provided a valuable tool for functional prediction of unknown proteins. For the evaluation of PID matrix, cross validation was performed with subsets of DIP data. The prediction system gives about 50% sensitivity and more than 98% specificity, which implies that the information for interacting proteins pairs could be enriched about 30 fold with the PID matrix.It is demonstrated that mapping of the genome-wide interaction network can be achieved by using the PID matrix.
机译:蛋白质 - 蛋白质相互作用在生物过程中起着关键作用。通过计算方法识别蛋白质可以提供在不进行广泛的实验的情况下的功能研究中的新铅。我们为从实验识别的相互作用蛋白对数据集(DIP:蛋白质数据库)的数据集中提取的潜在交互域对(PID)的数据库进行了分解,蛋白质家族,结构域和功能位点的集成数据库。在开发蛋白质相互作用数据库和预测方法中,敏感的统计评分系统对于提供可靠性指标,以提供对交互网络的准确功能分析的可靠性指标至关重要。我们介绍统计评分系统,名为“PID矩阵分数”作为域之间的交互概率(交互性)的量度。该系统为未知蛋白质的功能预测提供了有价值的工具。对于PID矩阵的评估,使用DIP数据的子集执行交叉验证。预测系统提供了大约50%的灵敏度和超过98%的特异性,这意味着与PID矩阵的相互作用蛋白对的信息可以富集约30倍。这证明可以实现基因组相互作用网络的映射通过使用PID矩阵。

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