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. 2022 Oct 17;19(2):151–158. doi: 10.1038/s41589-022-01142-z

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© The Author(s) 2022

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. 6 — a, Size exclusion chromatogram of wild-type ClbP purified in GDN. Protein eluted in the fraction bound by the vertical lines was used for cryo-EM analysis. b, Representative micrograph of ClbP embedded in vitreous ice (scale bar = 600 Å; from 3888 micrographs), low pass and high pass filtered for clarity. c, Selected 2D class averages of ClbP. d, Reconstruction of ClbP filtered and colored by local resolution. Complete data analysis procedure is in Extended Data Fig. 7a. e, Gold-standard Fourier shell correlation (FSC) curves from cryoSPARC. f, Viewing direction distribution plot.

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