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. 2024 Aug 29;15:7511. doi: 10.1038/s41467-024-51754-3

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, 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 licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

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Fig. 7 — a Comparison of the different particle populations isolated by different bait proteins used in this study. b–d Effects of usnic acid on the Nsa1-TAP particle population. b The (shifting) particle populations and the cryo-EM map of the respective clusters (1–4) (see Figs. 5, 6), c their 25S rRNA domain folding state, d maturation factor association/dissociation (see Fig. 4a, b, d, e) as well as e pre-rRNA processing states. The dashed blue line indicates the block in ribosome formation due to usnic acid treatment. For simplicity, rebound effects on earlier stages are not shown.