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Improving sequence-based fold recognition by using 3D model quality assessment

机译:通过使用3D模型质量评估来改善基于序列的折叠识别

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Motivation: The ability of a simple method (MODCHECK) to determine the sequence-structure compatibility of a set of structural models generated by fold recognition is tested in a thorough benchmark analysis. Four Model Quality Assessment Programs (MQAPs) were tested on 188 targets from the latest LiveBench-9 automated structure evaluation experiment. We systematically test and evaluate whether the MQAP methods can successfully detect native-likemodels.Results: We show that compared with the other three methods tested MODCHECK is the most reliable method for consistently performing the best top model selection and for ranking the models. In addition, we show that the choice of model similarity score used to assess a model's similarity to the experimental structure can influence the overall performance of these tools. Although these MQAP methods fail to improve the model selection performance for methods that already incorporate protein three dimension (3D) structural information, an improvement is observed for methods that are purely sequence-based, including the best profile-profile methods. This suggests that even the best sequence-based fold recognition methods can still be improved by taking into account the 3D structural information.
机译:动机:在彻底的基准分析中测试了一种简单方法(MODCHECK)确定由折叠识别生成的一组结构模型的序列结构兼容性的能力。最新的LiveBench-9自动结构评估实验对188个目标测试了四个模型质量评估程序(MQAP)。我们系统地测试和评估了MQAP方法是否可以成功检测到类似本机的模型。结果:与其他三种测试方法相比,MODCHECK是始终执行最佳顶级模型选择和模型排名的最可靠方法。此外,我们表明,用于评估模型与实验结构相似性的模型相似性评分的选择会影响这些工具的整体性能。尽管这些MQAP方法无法改善已经包含蛋白质三维(3D)结构信息的方法的模型选择性能,但是可以观察到纯基于序列的方法(包括最佳的图谱图谱方法)得到了改善。这表明,即使考虑到最佳的基于序列的折叠识别方法,也可以通过考虑3D结构信息来进行改进。

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