Abstract 2235 Viral SF1B helicases as antiviral targets

The successful development of inhibitors to viral enzymes like the RNA-dependent RNA polymerase and protease that exhibit broad-spectrum activity support the general notion that viral enzymes are tractable drug targets. Plus-strand RNA viruses of animals encode a helicase, although helicase activity has not been demonstrated for all. Alphaviruses (chikungunya virus, CHIKV) and coronaviruses (severe acute respiratory syndrome coronavirus 2, SARS2) encode superfamily 1B (SF1B) helicases that translocate in a 5'->3' direction.

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Publication Details

Journal
Journal of Biological Chemistry
Published
2025-05-01
DOI
https://doi.org/10.1016/j.jbc.2025.109182
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
0.00
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Abstract 2235 Viral SF1B helicases as antiviral targets

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Abstract 2235 Viral SF1B helicases as antiviral targets

Jamie Arnold, Kacey M. Talbot, Marilyn McLean, Craig E. Cameron, Yuan-Wei Su, Jake Royster
article en

Abstract

The successful development of inhibitors to viral enzymes like the RNA-dependent RNA polymerase and protease that exhibit broad-spectrum activity support the general notion that viral enzymes are tractable drug targets. Plus-strand RNA viruses of animals encode a helicase, although helicase activity has not been demonstrated for all. Alphaviruses (chikungunya virus, CHIKV) and coronaviruses (severe acute respiratory syndrome coronavirus 2, SARS2) encode superfamily 1B (SF1B) helicases that translocate in a 5'->3' direction.

Journal of Biological ChemistryVol. 301(5)
University of North Carolina at Chapel Hill (US)
Zero hunger
Openalex Percentile: Top 88%
RNA modifications and cancer
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