Flavin-dependent thymidylate synthase: N5 of flavin as a Methylene carrier.

Kalani Karunaratne, Nicholas Luedtke, Daniel M Quinn, Amnon Kohen

Journal: Archives of biochemistry and biophysics 2017;632():11-19

PMID: 28821425

Abstract

Thymidylate is synthesized de novo in all living organisms for replication of genomes. The chemical transformation is reductive methylation of deoxyuridylate at C5 to form deoxythymidylate. All eukaryotes including humans complete this well-understood transformation with thymidylate synthase utilizing 6R-N-N-methylene-5,6,7,8-tetrahydrofolate as both a source of methylene and a reducing hydride. In 2002, flavin-dependent thymidylate synthase was discovered as a new pathway for de novo thymidylate synthesis. The flavin-dependent catalytic mechanism is different than thymidylate synthase because it requires flavin as a reducing agent and methylene transporter. This catalytic mechanism is not well-understood, but since it is known to be very different from thymidylate synthase, there is potential for mechanism-based inhibitors that can selectively inhibit the flavin-dependent enzyme to target many human pathogens with low host toxicity.

Copyright © 2017 Elsevier Inc. All rights reserved.

Address: Department of Chemistry, University of Iowa, Iowa City, IA 52242, USA.; Department of Chemistry, University of Iowa, Iowa City, IA 52242, USA. Electronic address: [email protected].
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