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本文引用的文献

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Quality assessment for the putative intrinsic disorder in proteins.蛋白质内源性无序的质量评估。
Bioinformatics. 2019 May 15;35(10):1692-1700. doi: 10.1093/bioinformatics/bty881.
2
Prediction of protein disorder based on IUPred.基于IUPred的蛋白质无序预测。
Protein Sci. 2018 Jan;27(1):331-340. doi: 10.1002/pro.3334. Epub 2017 Nov 16.
3
Mobi 2.0: an improved method to define intrinsic disorder, mobility and linear binding regions in protein structures.Mobi 2.0:一种改进的方法,用于定义蛋白质结构中的固有无序、流动性和线性结合区域。
Bioinformatics. 2018 Jan 1;34(1):122-123. doi: 10.1093/bioinformatics/btx592.
4
Computational Prediction of Intrinsic Disorder in Proteins.蛋白质内在无序性的计算预测
Curr Protoc Protein Sci. 2017 Apr 3;88:2.16.1-2.16.14. doi: 10.1002/cpps.28.
5
Effect of Intrinsic Disorder and Self-Association on the Translational Diffusion of Proteins: The Case of α-Casein.内在无序和自缔合对蛋白质平移扩散的影响:以α-酪蛋白为例。
J Phys Chem B. 2017 Apr 13;121(14):2980-2988. doi: 10.1021/acs.jpcb.7b00772. Epub 2017 Mar 31.
6
How disordered is my protein and what is its disorder for? A guide through the "dark side" of the protein universe.我的蛋白质有多无序,其无序状态又是为何?蛋白质世界“黑暗面”指南。
Intrinsically Disord Proteins. 2016 Dec 21;4(1):e1259708. doi: 10.1080/21690707.2016.1259708. eCollection 2016.
7
CIDER: Resources to Analyze Sequence-Ensemble Relationships of Intrinsically Disordered Proteins.CIDER:用于分析内在无序蛋白质序列-集合关系的资源。
Biophys J. 2017 Jan 10;112(1):16-21. doi: 10.1016/j.bpj.2016.11.3200.
8
DisProt 7.0: a major update of the database of disordered proteins.DisProt 7.0:无序蛋白质数据库的重大更新。
Nucleic Acids Res. 2017 Jan 4;45(D1):D219-D227. doi: 10.1093/nar/gkw1056. Epub 2016 Nov 28.
9
Sequence Determinants of the Conformational Properties of an Intrinsically Disordered Protein Prior to and upon Multisite Phosphorylation.序列决定了无规卷曲蛋白质在多位点磷酸化前后的构象特性。
J Am Chem Soc. 2016 Nov 30;138(47):15323-15335. doi: 10.1021/jacs.6b10272. Epub 2016 Nov 17.
10
A collection of intrinsic disorder characterizations from eukaryotic proteomes.真核生物蛋白质组中内无序特性的集合。
Sci Data. 2016 Jun 21;3:160045. doi: 10.1038/sdata.2016.45.

有必要制定用于描述和报告蛋白质内无序的指南。

On the Need to Develop Guidelines for Characterizing and Reporting Intrinsic Disorder in Proteins.

机构信息

Interdisciplinary Biological Sciences, Northwestern University, Evanston, IL, 60208, USA.

Department of Molecular Medicine and USF Health Byrd Alzheimer's Research Institute, Morsani College of Medicine, University of South Florida, Tampa, Florida, 33612, USA.

出版信息

Proteomics. 2019 Mar;19(6):e1800415. doi: 10.1002/pmic.201800415. Epub 2019 Mar 1.

DOI:10.1002/pmic.201800415
PMID:30793871
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6571172/
Abstract

Since the early 2000s, numerous computational tools have been created and used to predict intrinsic disorder in proteins. At present, the output from these algorithms is difficult to interpret in the absence of standards or references for comparison. There are many reasons to establish a set of standard-based guidelines to evaluate computational protein disorder predictions. This viewpoint explores a handful of these reasons, including standardizing nomenclature to improve communication, rigor and reproducibility, and making it easier for newcomers to enter the field. An approach for reporting predicted disorder in single proteins with respect to whole proteomes is discussed. The suggestions are not intended to be formulaic; they should be viewed as a starting point to establish guidelines for interpreting and reporting computational protein disorder predictions.

摘要

自 21 世纪初以来,已经创建并使用了许多计算工具来预测蛋白质中的内在无序。目前,由于缺乏标准或参考物进行比较,这些算法的输出结果难以解释。建立一套基于标准的准则来评估计算蛋白质无序预测有很多原因。本观点探讨了其中的一些原因,包括通过标准化命名法来提高沟通、严谨性和可重复性,以及为新进入该领域的人提供便利。还讨论了一种针对整个蛋白质组中单蛋白预测无序的报告方法。这些建议并非一成不变的;它们应被视为建立解释和报告计算蛋白质无序预测的准则的起点。