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Combinatorial Optimization Algorithms for Metabolic Networks Alignments and Their Applications

机译:代谢网络对准的组合优化算法及其应用

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The accumulation of high-throughput genomic and proteomic data allows for reconstruction of large and complex metabolic networks. To analyze accumulated data and reconstructed networks, it is critical to identify network patterns and evolutionary relations between metabolic networks; finding similar networks is computationally challenging. Based on gene duplication and function sharing in biological networks, a network alignment problem is formulated that asks the optimal vertex-to-vertex mapping allowing path contraction, different types of vertex deletion, and vertex insertions. This paper presents fixed parameter tractable combinatorial optimization algorithms, which take into account the similarity of both the enzymes' functions arbitrary network topologies. Results are evaluated by the randomized P- Value computation. The authors perform pairwise alignments of all pathways for four organisms and find a set of statistically significant pathway similarities. The network alignment is used to identify pathway holes that are the result of inconsistencies and missing enzymes. The authors propose a framework of filling pathway holes by including database searches for missing enzymes and proteins with the matching prosites and further finding potential candidates with high sequence similarity.
机译:高通量基因组和蛋白质组学数据的积累可以重建大型复杂的代谢网络。为了分析积累的数据和重建的网络,识别网络模式和代谢网络之间的进化关系至关重要。寻找类似的网络在计算上具有挑战性。基于生物网络中的基因复制和功能共享,提出了一种网络对齐问题,该问题要求最优的顶点到顶点映射,以允许路径收缩,不同类型的顶点删除和顶点插入。本文提出了固定参数易处理的组合优化算法,该算法考虑了两种酶的功能的相似性以及任意网络拓扑。通过随机P值计算评估结果。作者对四种生物的所有途径进行了成对比对,发现了一组统计学上显着的途径相似性。网络比对用于识别不一致和缺少酶的结果导致的通路孔。作者提出了一种填补途径漏洞的框架,方法是包括通过数据库搜索匹配的脯氨酸缺失的酶和蛋白质,并进一步寻找具有高度序列相似性的潜在候选物。

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