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Multiscale Visual Drilldown for the Analysis of Large Ensembles of Multi-Body Protein Complexes

机译:用于大规模分析多体蛋白复合物的多尺度可视化深入分析

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When studying multi-body protein complexes, biochemists use computational tools that can suggest hundreds or thousands of their possible spatial configurations. However, it is not feasible to experimentally verify more than only a very small subset of them. In this paper, we propose a novel multiscale visual drilldown approach that was designed in tight collaboration with proteomic experts, enabling a systematic exploration of the configuration space. Our approach takes advantage of the hierarchical structure of the data from the whole ensemble of protein complex configurations to the individual configurations, their contact interfaces, and the interacting amino acids. Our new solution is based on interactively linked 2D and 3D views for individual hierarchy levels. At each level, we offer a set of selection and filtering operations that enable the user to narrow down the number of configurations that need to be manually scrutinized. Furthermore, we offer a dedicated filter interface, which provides the users with an overview of the applied filtering operations and enables them to examine their impact on the explored ensemble. This way, we maintain the history of the exploration process and thus enable the user to return to an earlier point of the exploration. We demonstrate the effectiveness of our approach on two case studies conducted by collaborating proteomic experts.
机译:在研究多体蛋白质复合物时,生物化学家使用可以建议数百或数千种可能的空间构型的计算工具。但是,仅通过实验中的一小部分进行验证是不可行的。在本文中,我们提出了一种新颖的多尺度可视化向下钻取方法,该方法是在与蛋白质组学专家紧密合作的基础上设计的,从而可以对配置空间进行系统的探索。我们的方法利用了从蛋白质复合物整个配置到单个配置,它们的接触界面以及相互作用的氨基酸的整体数据层次结构。我们的新解决方案基于针对各个层次结构级别的交互式链接的2D和3D视图。在每个级别,我们提供了一组选择和过滤操作,使用户能够缩小需要手动检查的配置的数量。此外,我们提供了专用的过滤器界面,该界面为用户提供了所应用的过滤操作的概述,并使他们能够检查其对所探索集合的影响。这样,我们可以维护探索过程的历史,从而使用户能够返回到探索的更早点。我们在蛋白质组学专家合作进行的两个案例研究中证明了我们的方法的有效性。

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