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. 2017 May 16;45(11):6613–6627. doi: 10.1093/nar/gkx417

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© The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Figure 4. — Identification of MPK6-phosphorylation sites on MYB15 by site-directed mutagenesis. Coomassie Brilliant Blue (CBB) staining and autoradiography of an SDS-polyacrylamide gel with resolved kinase reactions containing the indicated combinations of purified Escherichia coli-expressed proteins and [γ-³²P] ATP. The mutant full-length MYB15 proteins MYB15^T18A, MYB15^S168A and MYB15^T18A/S168A (MYB15^AA) were generated by site-directed mutagenesis. Myelin basic protein (MBP) and GST were used as positive and negative controls, respectively.