Correlation Engine 2.0
Clear Search sequence regions

Sizes of these terms reflect their relevance to your search.

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. Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.


Tristan J Smart, Refaat B Hamed, Timothy D W Claridge, Christopher J Schofield. Studies on the selectivity of proline hydroxylases reveal new substrates including bicycles. Bioorganic chemistry. 2020 Jan;94:103386

Expand section icon Mesh Tags

Expand section icon Substances

PMID: 31706681

View Full Text