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Studies on the selectivity of proline hydroxylases reveal new substrates including bicycles
Smart, T.J. Hamed, Refaat B. Claridge, T.D.W. Schofield, C.J.
Smart, T.J.
Hamed, Refaat B.
Claridge, T.D.W.
Schofield, C.J.
Publication Date
2020-01
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(c) 2020 The Authors. This is an Open Access article distributed under the Creative Commons CC-BY license (https://creativecommons.org/licenses/by/4.0/)
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2019-10-21
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Abstract
Studies on the substrate selectivity of recombinant ferrous-iron- and 2-oxoglutarate-dependent proline hydroxylases (PHs) reveal that they can catalyse the production of dihydroxylated 5-, 6-, and 7-membered ring products, and can accept bicyclic substrates. Ring-substituted substrate analogues (such hydroxylated and fluorinated prolines) are accepted in some cases. The results highlight the considerable, as yet largely untapped, potential for amino acid hydroxylases and other 2OG oxygenases in biocatalysis.
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Smart TJ, Hamed RB, Claridge TDW et al (2020) Studies on the selectivity of proline hydroxylases reveal new substrates including bicycles. Bioorganic Chemistry. 94: 103386.
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