UL21 is a conserved protein in the tegument of alphaherpesviruses and has multiple important albeit poorly understood functions in viral replication and pathogenesis. To provide a roadmap for exploration of the multiple roles of UL21, we determined the crystal structure of its conserved N-terminal domain from herpes simplex virus 1 to 2.0-Å resolution, which revealed a novel sail-like protein fold. Evolutionarily conserved surface patches highlight residues of potential importance for future targeting by mutagenesis.
CITATION STYLE
Metrick, C. M., Chadha, P., & Heldwein, E. E. (2015). The Unusual Fold of Herpes Simplex Virus 1 UL21, a Multifunctional Tegument Protein. Journal of Virology, 89(5), 2979–2984. https://doi.org/10.1128/jvi.03516-14
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