Correction: Proteome-wide characterization of PTMs reveals host cell responses to viral infection and identifies putative antiviral drug targets

Affiliations

¹ Biological Sciences Division, Pacific Northwest National Laboratory, Pacific Northwest National Laboratory, Richland, WA, United States.
² Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, WA, United States.
³ Hanford High School, Richland, WA, United States.
⁴ Nuclear Chemical & Biological Technologies Division, Pacific Northwest National Laboratory, Richland, WA, United States.

Published Erratum

Xiaolu Li et al. Front Immunol. 2025.

. 2025 Aug 12:16:1672766.

doi: 10.3389/fimmu.2025.1672766. eCollection 2025.

¹ Biological Sciences Division, Pacific Northwest National Laboratory, Pacific Northwest National Laboratory, Richland, WA, United States.
² Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, WA, United States.
³ Hanford High School, Richland, WA, United States.
⁴ Nuclear Chemical & Biological Technologies Division, Pacific Northwest National Laboratory, Richland, WA, United States.

Abstract

[This corrects the article DOI: 10.3389/fimmu.2025.1587106.].

Keywords: PTMs; acetylation; antiviral drug; phosphorylation; proteome; redox; ubiquitination; viral infection.

Proteome-wide characterization of PTMs reveals host cell responses to viral infection and identifies putative antiviral drug targets.
Li X, Kabza A, Ives AN, Thiel J, Waters KM, Qian WJ, Sims AC, Zhang T. Li X, et al. Front Immunol. 2025 May 30;16:1587106. doi: 10.3389/fimmu.2025.1587106. eCollection 2025. Front Immunol. 2025. PMID: 40519923 Free PMC article. Review.