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. 2021 Dec 28;29(1):10–20. doi: 10.1038/s41594-021-00698-z

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© The Author(s) 2021

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. 5 — a, MCM peptide phosphorylation drops by 92% following DDK preautophosphorylation. b, MCM–Cdt1 phosphorylation is abrogated following DDK preautophosphorylation. c, DH phosphorylation is virtually unperturbed following DDK preautophosphorylation. a–c, Representative images of three independent experiments. d, 2D averages derived from negatively stained particles indicating that DDK binding to DHs is unperturbed following DDK preautophosphorylation. Uncropped images for a and c are available as Source data with the paper online.

Source data