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PROTEIN STRUCTURE ALIGNMENT AND FAST SIMILARITY SEARCH USING LOCAL SHAPE SIGNATURES

机译:蛋白质结构对齐和快速相似性使用本地形状签名进行搜索

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摘要

We present a new method for conducting protein structure similarity searches, which improves on the efficiency of some existing techniques. Our method is grounded in the theory of differential geometry on 3D space curve matching. We generate shape signatures for proteins that are invariant, localized, robust, compact, and biologically meaningful. The invariancy of the shape signatures allows us to improve similarity searching efficiency by adopting a hierarchical coarse-to-fine strategy. We index the shape signatures using an efficient hashing-based technique. With the help of this technique we screen out unlikely candidates and perform detailed pairwise alignments only for a small number of candidates that survive the screening process. Contrary to other hashing based techniques, our technique employs domain specific information (not just geometric information) in constructing the hash key, and hence, is more tuned to the domain of biology. Furthermore, the invariancy, localization, and compactness of the shape signatures allow us to utilize a well-known local sequence alignment algorithm for aligning two protein structures. One measure of the efficacy of the proposed technique is that we were able to perform structure alignment queries 36 times faster (on the average) than a well-known method while keeping the quality of the query results at an approximately similar level.
机译:我们提出了一种进行蛋白质结构相似性搜索的新方法,这提高了一些现有技术的效率。我们的方法基于3D空间曲线匹配的差分几何理论。我们为不变,局部,鲁棒,紧凑和生物有意义的蛋白质产生形状签名。形状签名的INRARARCY通过采用分层粗略策略来提高相似性搜索效率。我们使用基于有效的散列技术索引形状签名。在这种技术的帮助下,我们屏蔽了不太可能的候选人,仅针对少量候选的候选者进行详细的成对对齐。与基于其他散列的技术相反,我们的技术在构建散列键时使用域特定信息(不仅仅是几何信息),因此,更调谐到生物学领域。此外,形状签名的InorRARCY,定位和紧凑性允许我们利用众所周知的局部序列对准算法来对准两个蛋白质结构。提出技术的效力的一个衡量标准是,我们能够比众所周知的方法更快地(平均)执行结构对准查询36倍(平均值),同时保持查询的质量结果在大致相似的水平上。

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