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. 2021 Jan 13;11:928. doi: 10.1038/s41598-020-79031-5

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© The Author(s) 2021

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 licence, and indicate if changes were made. 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/4.0/.

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Homology alignment between IsPETase and Cut190*. (A) PyMOL structural alignment of Cut190* with IsPETase. MacPyMOL (ver 1.8.6.2) was used to perform the structural alignment³². IsPETase is pink (PDB: 6EQE¹³); Cut190* is blue (PDB: 5ZNO⁵). (B) Residues mutated to generate disulfide bridge in Cut190* (E296 and D250) align with S282 and N233 in IsPETase.