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代谢途径的一致排列,无需抽象化。

Consistent alignment of metabolic pathways without abstraction.

作者信息

Ay Ferhat, Kahveci Tamer, de Crécy-Lagard Valerie

机构信息

Department of Computer Science and Engineering, University of Florida, Gainesville, FL 32611, USA.

出版信息

Comput Syst Bioinformatics Conf. 2008;7:237-48.

Abstract

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.

摘要

代谢途径展示了不同的生化实体如何相互作用,以执行对生物体生存至关重要的功能。代谢途径之间的相似性表明了功能上的相似性,而仅通过比较构成这些途径的单个实体很难识别这种相似性。当相互作用的实体为单一类型时,识别相似性的问题就简化为图同构问题。然而,对于具有不同类型实体的代谢途径,比如代谢途径,比对问题更具挑战性。现有的方法通常通过忽略除一种类型之外的所有实体来解决代谢途径比对问题。这种抽象化显著降低了比对的相关性,因为它导致了信息内容的损失。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。我们方法的一个显著特点是它在不抽象代谢途径的情况下对反应、化合物和酶进行比对。我们基于这样一种直觉,即实体的成对相似性(同源性)及其组织(拓扑结构)对于代谢途径比对都至关重要。在我们的算法中,我们通过为每种实体类型创建一个特征值问题来兼顾这两者。我们通过考虑比对实体的可达集来强制保持一致性。我们的实验表明,对于大约有100个实体的代谢途径,我们的方法能在数秒内找到具有生物学和统计学意义的比对结果。

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