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. 2022 Mar 3;13:1137. doi: 10.1038/s41467-022-28722-w

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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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Fig. 2 — a Two cartoon representations showing the general fold and secondary structure organization of EndoE-GH18L, including the GH18 domain (yellow), the 3HB-1 (dark orange), and 3HB-2 (light gray) domains, and the α12 linker (light blue). b Two electrostatic surface representations of EndoE-GH18L showing the location of the putative N-glycan binding site and the catalytic site. c Two surface representations of the GH18 domain of EndoE, with annotated domains and loops. d Close-up view of the active site of the GH18 domain of EndoE shown as cartoon/stick representation (yellow). e Close-up view of the active site of the GH18 domain of EndoE shown as electrostatic surface representation. f Close-up view of the active site of the GH18 domain of EndoE shown with annotated loops.