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. 2018 Jul 12;8:10557. doi: 10.1038/s41598-018-28836-6

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© The Author(s) 2018

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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(A) SPR sensorgrams for qualitative comparison of bindings for P_hNgb1-Wt, P_hNgb1-M₁, and P_hNgb1-M₂. (B) SPR sensorgrams for inhibition of P_hNgb1-Wt binding by P_{Cyt c}. (C) SPR sensorgrams for qualitative comparison of bindings for P_hNgb2-Wt, P_hNgb2-M₁, and P_hNgb2-M₂. Black arrows in Fig. A to Fig. C show starting time of analyte injections. All peptides were injected for 60 s. (D) Distance between E86 (hNgb) and K27 (Cyt c) residues. The dotted line is drawn to show a reference line at 5 Å for salt bridge.