一致的排列代谢途径没有抽象。

F. Ay, Tamer Kahveci, V. de Crécy-Lagard
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引用次数: 16

摘要

途径显示了不同的生化实体如何相互作用,以执行生物体生存的重要功能。途径之间的相似性表明,很难通过比较构成这些途径的单个实体来识别功能上的相似性。当交互实体为单一类型时,识别相似度的问题可简化为图同构问题。然而,对于具有不同类型实体的路径,如代谢路径,对齐问题更具挑战性。现有的方法通常通过忽略除一种类型外的所有实体来解决代谢途径对齐问题。这种抽象显著地降低了对齐的相关性,因为它会导致信息内容的丢失。在本文中,我们开发了一种方法来解决代谢途径的成对比对问题。我们的方法的一个显著特点是,它对齐反应,化合物和酶没有抽象的途径。我们追求的直觉是,实体的两两相似性(同源性)和它们的组织(拓扑)对代谢途径对齐至关重要。在我们的算法中,我们通过为每个实体类型创建一个特征值问题来解释这两个问题。我们通过考虑对齐实体的可达性集来增强一致性。我们的实验表明,我们的方法在大约100个实体的路径中以秒为单位发现了生物学和统计学上显著的对齐。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Consistent alignment of metabolic pathways without abstraction.
Pathways show how different biochemical entities interact with each other to perform vital functions for the survival of organisms. Similarities between pathways indicate functional similarities that are difficult to identify by comparing the individual entities that make up those pathways. When interacting entities are of single type, the problem of identifying similarities reduces to graph isomorphism problem. However, for pathways with varying types of entities, such as metabolic pathways, alignment problem is more challenging. Existing methods, often, address the metabolic pathway alignment problem by ignoring all the entities except for one type. This kind of abstraction reduces the relevance of the alignment significantly as it causes losses in the information content. In this paper, we develop a method to solve the pairwise alignment problem for metabolic pathways. One distinguishing feature of our method is that it aligns reactions, compounds and enzymes without abstraction of pathways. We pursue the intuition that both pairwise similarities of entities (homology) and their organization (topology) are crucial for metabolic pathway alignment. In our algorithm, we account for both by creating an eigenvalue problem for each entity type. We enforce the consistency by considering the reachability sets of the aligned entities. Our experiments show that, our method finds biologically and statistically significant alignments in the order of seconds for pathways with approximately 100 entities.
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