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. 2018 Jan 18;8:1045. doi: 10.1038/s41598-018-19295-0

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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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CHIKV nsP1 modulates the ATPase activity of nsP2-NT in vitro. (a) The ATPase activity was assessed for CHIKV S 27 nsP2-NT and nsP1-WT. The TLC plate was exposed to the X-Ray film and the image was developed. The unlabelled ATP (cold ATP) was used as competitor. (b) Bar diagram showing the relative intensities of free γ-P³² spots that were released by S 27 nsP1-WT/nsP2-NT alone or together. (c) The bar diagram represents the ATPase activities of nsP1-WT or nsP2-NT alone or together which were measured by colorimetric assay. (d) The line diagram showing the ATPase activities of nsP1-WT or nsP2-NT with increasing concentrations of nsP1-WT as measured by colorimetric assay. The data represent mean ± SEM of at least three independent experiments. The p-value ≤ 0.05 was considered as statistically significant difference between the groups. (*P ≤ 0.05).