Royal Society of Chemistry, RSC Chemical Biology, 3(4), p. 235-243, 2023
DOI: 10.1039/d2cb00182a
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Ribosomal histidine hydroxylases MINA53 and NO66 exhibit narrow substrate selectivities for ribosomal protein L27a/L8 peptides possessing histidine analogues. Selected Rpl peptides display potent inhibition against MINA53 and NO66, providing a basis for inhibitor design.