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. 2021 Mar 1;11:4857. doi: 10.1038/s41598-021-84218-5

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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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Captopril methylation by His-GST-METTL7B at various AdoMet concentrations in the presence or absence of AdoHcy: (A) His-GST-METTL7B catalyzed AdoMet-dependent methylation of captopril exhibits saturable Michaelis–Menten kinetics. Peak area ratio of methyl captopril to internal standard (PAR) versus concentration of AdoMet. (B) Inhibition of His-GST-METTL7B captopril methylation by AdoHcy. PAR versus AdoMet concentration curve at varying concentrations of AdoHcy. Data presented as mean ± s.d. n = 3 for (A) and average ± error (n = 2) for (B).