Department of Computer Science and Software Engineering, Auburn University, Auburn, Alabama, United States of America.
Department of Biological Sciences, Auburn University, Auburn, Alabama, United States of America.
PLoS One. 2020 Feb 13;15(2):e0228245. doi: 10.1371/journal.pone.0228245. eCollection 2020.
Significant advancements in the field of protein structure prediction have necessitated the need for objective and robust evaluation of protein structural models by comparing predicted models against the experimentally determined native structures to quantitate their structural similarities. Existing protein model versus native similarity metrics either consider the distances between alpha carbon (Cα) or side-chain atoms for computing the similarity. However, side-chain orientation of a protein plays a critical role in defining its conformation at the atomic-level. Despite its importance, inclusion of side-chain orientation in structural similarity evaluation has not yet been addressed. Here, we present SPECS, a side-chain-orientation-included protein model-native similarity metric for improved evaluation of protein structural models. SPECS combines side-chain orientation and global distance based measures in an integrated framework using the united-residue model of polypeptide conformation for computing model-native similarity. Experimental results demonstrate that SPECS is a reliable measure for evaluating structural similarity at the global level including and beyond the accuracy of Cα positioning. Moreover, SPECS delivers superior performance in capturing local quality aspect compared to popular global Cα positioning-based metrics ranging from models at near-experimental accuracies to models with correct overall folds-making it a robust measure suitable for both high- and moderate-resolution models. Finally, SPECS is sensitive to minute variations in side-chain χ angles even for models with perfect Cα trace, revealing the power of including side-chain orientation. Collectively, SPECS is a versatile evaluation metric covering a wide spectrum of protein modeling scenarios and simultaneously captures complementary aspects of structural similarities at multiple levels of granularities. SPECS is freely available at http://watson.cse.eng.auburn.edu/SPECS/.
蛋白质结构预测领域的重大进展使得有必要通过将预测模型与实验确定的天然结构进行比较,以量化它们的结构相似性,从而对蛋白质结构模型进行客观和稳健的评估。现有的蛋白质模型与天然相似性度量标准要么考虑α碳原子(Cα)之间的距离,要么考虑侧链原子之间的距离来计算相似性。然而,蛋白质的侧链取向在定义其原子水平构象方面起着关键作用。尽管如此,侧链取向在结构相似性评估中的纳入尚未得到解决。在这里,我们提出了 SPECS,这是一种包含侧链取向的蛋白质模型与天然相似性度量标准,用于改进蛋白质结构模型的评估。SPECS 将侧链取向和全局距离度量结合在一个综合框架中,使用多肽构象的统一残基模型来计算模型与天然结构的相似性。实验结果表明,SPECS 是一种可靠的度量标准,可以在全局范围内评估结构相似性,包括但不限于 Cα 定位的准确性。此外,与基于流行的全局 Cα 定位的指标相比,SPECS 在捕捉局部质量方面表现出更好的性能,这些指标涵盖了从接近实验精度的模型到具有正确整体折叠的模型,使其成为一种适用于高分辨率和中等分辨率模型的稳健度量标准。最后,SPECS 对侧链 χ 角的微小变化很敏感,即使对于具有完美 Cα 轨迹的模型也是如此,这揭示了包含侧链取向的威力。总之,SPECS 是一种通用的评估指标,涵盖了广泛的蛋白质建模场景,并同时在多个粒度水平上捕捉结构相似性的互补方面。SPECS 可在 http://watson.cse.eng.auburn.edu/SPECS/ 上免费获取。