Tang, Qingyun orcid.org/0000-0001-5517-5973 (2021) From Natural Methylation to Versatile Alkylations Using Halide Methyltransferases. Chembiochem. pp. 2584-2590. ISSN 1439-7633
Abstract
Naturally occurring and engineered promiscuous halide methyltransferases (HMTs) enable S-adenosyl-l-methionine analogues to be enzymatically synthesised and recycled, using simple and readily available alkyl iodides as alkyl donors. In combination with promiscuous methyltransferases (MTs), they dramatically expand the bioalkylation toolbox.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © 2021 The Authors. |
Dates: |
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Institution: | The University of York |
Academic Units: | The University of York > Faculty of Sciences (York) > Chemistry (York) |
Depositing User: | Pure (York) |
Date Deposited: | 09 Sep 2022 09:30 |
Last Modified: | 16 Oct 2024 18:43 |
Published Version: | https://doi.org/10.1002/cbic.202100153 |
Status: | Published |
Refereed: | Yes |
Identification Number: | 10.1002/cbic.202100153 |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:190865 |
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Description: From Natural Methylation to Versatile Alkylations Using Halide Methyltransferases
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