Literature DB >> 29709390

Amazing Diversity in Biochemical Roles of Fe(II)/2-Oxoglutarate Oxygenases.

Caitlyn Q Herr1, Robert P Hausinger2.   

Abstract

Since their discovery in the 1960s, the family of Fe(II)/2-oxoglutarate-dependent oxygenases has undergone a tremendous expansion to include enzymes catalyzing a vast diversity of biologically important reactions. Recent examples highlight roles in controlling chromatin modification, transcription, mRNA demethylation, and mRNA splicing. Others generate modifications in tRNA, translation factors, ribosomes, and other proteins. Thus, oxygenases affect all components of molecular biology's central dogma, in which information flows from DNA to RNA to proteins. These enzymes also function in biosynthesis and catabolism of cellular metabolites, including antibiotics and signaling molecules. Due to their critical importance, ongoing efforts have targeted family members for the development of specific therapeutics. This review provides a general overview of recently characterized oxygenase reactions and their key biological roles.
Copyright © 2018 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Nonheme iron oxygenase; biodegradation; biosynthesis; chromatin modification; transcription; translation

Mesh:

Substances:

Year:  2018        PMID: 29709390      PMCID: PMC6014900          DOI: 10.1016/j.tibs.2018.04.002

Source DB:  PubMed          Journal:  Trends Biochem Sci        ISSN: 0968-0004            Impact factor:   13.807


  96 in total

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Review 3.  Glutarate L-2-hydroxylase (CsiD/GlaH) is an archetype Fe(II)/2-oxoglutarate-dependent dioxygenase.

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