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Analysis on multi-domain cooperation for predicting protein-protein interactions

机译:预测蛋白质相互作用的多域合作分析

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Background Domains are the basic functional units of proteins. It is believed that protein-protein interactions are realized through domain interactions. Revealing multi-domain cooperation can provide deep insights into the essential mechanism of protein-protein interactions at the domain level and be further exploited to improve the accuracy of protein interaction prediction. Results In this paper, we aim to identify cooperative domains for protein interactions by extending two-domain interactions to multi-domain interactions. Based on the high-throughput experimental data from multiple organisms with different reliabilities, the interactions of domains were inferred by a Linear Programming algorithm with Multi-domain pairs (LPM) and an Association Probabilistic Method with Multi-domain pairs (APMM). Experimental results demonstrate that our approach not only can find cooperative domains effectively but also has a higher accuracy for predicting protein interaction than the existing methods. Cooperative domains, including strongly cooperative domains and superdomains, were detected from major interaction databases MIPS and DIP, and many of them were verified by physical interactions from the crystal structures of protein complexes in PDB which provide intuitive evidences for such cooperation. Comparison experiments in terms of protein/domain interaction prediction justified the benefit of considering multi-domain cooperation. Conclusion From the computational viewpoint, this paper gives a general framework to predict protein interactions in a more accurate manner by considering the information of both multi-domains and multiple organisms, which can also be applied to identify cooperative domains, to reconstruct large complexes and further to annotate functions of domains. Supplementary information and software are provided in http://intelligent.eic.osaka-sandai.ac.jp/chenen/MDCinfer.htm and http://zhangroup.aporc.org/bioinfo/MDCinfer .
机译:背景结构域是蛋白质的基本功能单元。据信蛋白质-蛋白质相互作用是通过结构域相互作用实现的。揭示多域合作可以在域水平上深入了解蛋白质间相互作用的基本机制,并可以进一步用于提高蛋白质相互作用预测的准确性。结果在本文中,我们旨在通过将两结构域相互作用扩展为多结构域相互作用来识别蛋白质相互作用的协作域。基于来自具有不同可靠性的多个生物的高通量实验数据,通过具有多域对的线性规划算法(LPM)和具有多域对的关联概率方法(APMM)来推断域的相互作用。实验结果表明,与现有方法相比,我们的方法不仅可以有效地找到协作域,而且预测蛋白质相互作用的准确性更高。从主要的相互作用数据库MIPS和DIP中检测到了合作域,包括强合作域和超域,其中许多域通过PDB中蛋白质复合物的晶体结构的物理相互作用进行了验证,这为此类合作提供了直观的证据。在蛋白质/结构域相互作用预测方面的比较实验证明了考虑多结构域合作的益处。结论从计算的角度出发,本文通过考虑多域和多种生物的信息,提供了一个更准确地预测蛋白质相互作用的通用框架,该信息还可以用于识别协作域,重建大型复合体并进一步注释域的功能。在http://intelligent.eic.osaka-sandai.ac.jp/chenen/MDCinfer.htm和http://zhangroup.aporc.org/bioinfo/MDCinfer中提供了补充信息和软件。

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