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. 2017 Nov 13;7:15449. doi: 10.1038/s41598-017-15635-8

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© The Author(s) 2017

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Selection of sequences from the random dataset for experimental characterization. Scatter plot of the secondary structure (y-axis) and disorder prediction (x-axis) in which the selection of group 1 (green), 2 (blue), and 3 (red) proteins for experimental sampling is highlighted as circles (circles with 4-digit codes assigned were successfully purified and characterized). The secondary structure prediction is based on the overall average structure content stemming from five different predictors. The final disorder score is based on the z-value of the average rank of individual sequences from four different disorder predictors.