Q-score as a reliability measure for protein, nucleic acid and small-molecule atomic coordinate models derived from 3DEM maps.

IF 3.8 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Grigore Pintilie, Chenghua Shao, Zhe Wang, Brian P Hudson, Justin W Flatt, Michael F Schmid, Kyle L Morris, Stephen K Burley, Wah Chiu
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引用次数: 0

Abstract

Atomic coordinate models are important for the interpretation of 3D maps produced with cryoEM and cryoET (3D electron microscopy; 3DEM). In addition to visual inspection of such maps and models, quantitative metrics can inform about the reliability of the atomic coordinates, in particular how well the model is supported by the experimentally determined 3DEM map. A recently introduced metric, Q-score, was shown to correlate well with the reported resolution of the map for well fitted models. Here, we present new statistical analyses of Q-score based on its application to ∼10 000 maps and models archived in the EMDB (Electron Microscopy Data Bank) and PDB (Protein Data Bank). Further, we introduce two new metrics based on Q-score to represent each map and model relative to all entries in the EMDB and those with similar resolution. We explore through illustrative examples of proteins, nucleic acids and small molecules how Q-scores can indicate whether the atomic coordinates are well fitted to 3DEM maps and also whether some parts of a map may be poorly resolved due to factors such as molecular flexibility, radiation damage and/or conformational heterogeneity. These examples and statistical analyses provide a basis for how Q-scores can be interpreted effectively in order to evaluate 3DEM maps and atomic coordinate models prior to publication and archiving.

Q-score作为蛋白质、核酸和小分子原子坐标模型的可靠性测量,来源于3DEM地图。
原子坐标模型对于用cryoEM和cryoET (3D电子显微镜;3 dem)。除了对这些地图和模型进行目视检查外,定量指标还可以告知原子坐标的可靠性,特别是实验确定的3DEM地图对模型的支持程度。最近引入的一个度量,Q-score,被证明与良好拟合模型的地图分辨率有很好的相关性。在这里,我们基于Q-score在EMDB(电子显微镜数据库)和PDB(蛋白质数据库)中存档的约10,000个地图和模型中的应用,提出了新的Q-score统计分析。此外,我们引入了两个基于Q-score的新指标,以表示相对于EMDB中的所有条目和具有相似分辨率的条目的每个映射和模型。我们通过蛋白质,核酸和小分子的说明性示例探索q分数如何指示原子坐标是否与3DEM图很好地拟合,以及由于分子灵活性,辐射损伤和/或构象异质性等因素,地图的某些部分是否可能无法很好地解决。这些例子和统计分析为如何有效地解释q分数提供了基础,以便在出版和存档之前评估3DEM地图和原子坐标模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta Crystallographica. Section D, Structural Biology
Acta Crystallographica. Section D, Structural Biology BIOCHEMICAL RESEARCH METHODSBIOCHEMISTRY &-BIOCHEMISTRY & MOLECULAR BIOLOGY
CiteScore
4.50
自引率
13.60%
发文量
216
期刊介绍: Acta Crystallographica Section D welcomes the submission of articles covering any aspect of structural biology, with a particular emphasis on the structures of biological macromolecules or the methods used to determine them. Reports on new structures of biological importance may address the smallest macromolecules to the largest complex molecular machines. These structures may have been determined using any structural biology technique including crystallography, NMR, cryoEM and/or other techniques. The key criterion is that such articles must present significant new insights into biological, chemical or medical sciences. The inclusion of complementary data that support the conclusions drawn from the structural studies (such as binding studies, mass spectrometry, enzyme assays, or analysis of mutants or other modified forms of biological macromolecule) is encouraged. Methods articles may include new approaches to any aspect of biological structure determination or structure analysis but will only be accepted where they focus on new methods that are demonstrated to be of general applicability and importance to structural biology. Articles describing particularly difficult problems in structural biology are also welcomed, if the analysis would provide useful insights to others facing similar problems.
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