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. 2019 Apr 10;10:1659. doi: 10.1038/s41467-019-09655-3

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© The Author(s) 2019

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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Fig. 4 — SPR experiments with mStau2 dsRBD1 or dsRBD2. At low micromolar concentrations, mStau2 dsRBD1 alone binds neither to (a) SRS2 + 5 nor to (b) SRS*. In contrast, dsRBD2 binds to (c) SRS2 + 5 and to (d) SRS* with fast kinetics in a non-cooperative fashion with K_Ds of 650 nM or 829 nM, respectively. Steady-state binding curves are described by a Hill fit. ± indicates standard deviation. Source data are provided as a Source Data file