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. 2023 Feb 15;2(2):159–173. doi: 10.1038/s44161-023-00219-9

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© The Author(s) 2023

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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Extended Data Fig. 10 — a. Immunofluorescent micrograph of WT and ALPK3^mut hPSC-skeletal muscle stained for alpha actinin (green), SQSTM1 (magenta), and DAPI (blue). Scale bar = 15 µm. Line profile demonstrating alpha actinin and SQSTM1 organization. b. Graphical representation of select proteins bound to ALPK3 which also showed reduced phosphopeptide abundance in ALPK3^mut hPSC-CMs. The affected phosphorylation sites are also highlighted. Created with BioRender.com.