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. 2021 Jun 13;18(12):2617–2632. doi: 10.1080/15476286.2021.1935573

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© 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.

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Figure 5. — Cryo-EM structure of yeast ribosomes with bound rancRNA_18. (A) structure of the 60S ribosomal subunit (wheat) with highlighted rancRNA_18-dependent extra density (red), overlaid with the observed densities for P- and E-site tRNAs (blue) and the L1 stalk (green) in its closed conformation at 4.4 to 5.1 Å resolution. (B) representation of the 60S ribosomal subunit with rRNA in dark grey and ribosomal proteins in light grey. the observed rancRNA_18-dependent extra density (red), the two observed crosslinking site (C2675 and C2693, yellow),) and the L1 stalk (green) in its slight inward position are highlighted. (C) zoom into the rancRNA_18-dependent extra density (red) in close proximity to the observed crosslinking sites (C2675 and C2693, yellow) and r-protein L11 (uL5) (orange)