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. 2023 Oct 30;13:18610. doi: 10.1038/s41598-023-45428-1

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© The Author(s) 2023

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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Sequence alignment of homologous enzymes used to design mutations for enzyme activity enhancement. The L3-35A and X02A enzymes were sequence- and structurally-aligned against the most active enzymes on the fructosyl-hexapeptide F6P that are available in the literature, namely PnFPOX and FPOX-C⁶, AnFPOX-15 and AnFPOX-47²⁴. Yellow stars represent positions considered for mutagenesis.