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. 2020 Jan 15;10:393. doi: 10.1038/s41598-019-56825-w

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© The Author(s) 2020

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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Two distinct complexes of FprC151Stop D135N with HJ8/5. (A) Titration of HJ with Fpr. Complexes formed at the HJ: Fpr-dimer ratios of 0.25:1, 0.35:1, 0.5:1, 0.75:1, 1:1, 3:1, 6:1 separated on a native gel, stained with ethidium bromide to visualize DNA. (B) The gel above was stained by coomassie blue for protein. (C) Dissolved crystals of Fpr-HJ8/5 complex. Crystals extensively washed with well buffer were dissolved and analyzed on a native gel stained by coomassie blue. The final washing buffer had no detectable protein. Original full-length gels for Fig. 4 are shown in Supplementary Figure S9.