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. 2024 Apr 15;16(4):610. doi: 10.3390/v16040610

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© 2024 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).

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Schematic presentation of AALV1 (A), AoALV2 (B), AoALV3 (C) and AoALV4 (D) genomes with predicted ORFs and ribozymes (rbz) secondary structures drawn as inlay; black arrows show the potential self-cleavage site at the predicted HHRz and HPRz motifs. Conserved residues are highlighted in blue; (E) schematic representation of AoTV1 genome with predicted ORF and its conserved motifs. The rbz (+) polarity is defined as the RNA strand coding for the polymerase (ORF A). * nt positions of the region spanning the ribozyme in the original virus contig. For more information of the rbz position refer to Table S3.

Schematic presentation of AALV1 (A), AoALV2 (B), AoALV3 (C) and AoALV4 (D) genomes with predicted ORFs and ribozymes (rbz) secondary structures drawn as inlay; black arrows show the potential self-cleavage site at the predicted HHRz and HPRz motifs. Conserved residues are highlighted in blue; (E) schematic representation of AoTV1 genome with predicted ORF and its conserved motifs. The rbz (+) polarity is defined as the RNA strand coding for the polymerase (ORF A). * nt positions of the region spanning the ribozyme in the original virus contig. For more information of the rbz position refer to Table S3.