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Residues substitution and glycosylation analysis for E2 protein. The E2 protein sequences were aligned using the <t>MegAlign</t> program. The unique amino acid mutations were showed in black or red squares. The glycosylation sites were indicated with blue inverted triangle.
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Residues substitution and glycosylation analysis for E2 protein. The E2 protein sequences were aligned using the <t>MegAlign</t> program. The unique amino acid mutations were showed in black or red squares. The glycosylation sites were indicated with blue inverted triangle.
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Residues substitution and glycosylation analysis for E2 protein. The E2 protein sequences were aligned using the <t>MegAlign</t> program. The unique amino acid mutations were showed in black or red squares. The glycosylation sites were indicated with blue inverted triangle.
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Residues substitution and glycosylation analysis for E2 protein. The E2 protein sequences were aligned using the <t>MegAlign</t> program. The unique amino acid mutations were showed in black or red squares. The glycosylation sites were indicated with blue inverted triangle.
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Residues substitution and glycosylation analysis for E2 protein. The E2 protein sequences were aligned using the MegAlign program. The unique amino acid mutations were showed in black or red squares. The glycosylation sites were indicated with blue inverted triangle.

Journal: Frontiers in Microbiology

Article Title: Genomic characterization and evolutionary analysis of a Getah virus variant from piglets in central China

doi: 10.3389/fmicb.2025.1515632

Figure Lengend Snippet: Residues substitution and glycosylation analysis for E2 protein. The E2 protein sequences were aligned using the MegAlign program. The unique amino acid mutations were showed in black or red squares. The glycosylation sites were indicated with blue inverted triangle.

Article Snippet: The homology of isolate in this study with other reference strains was analyzed using the MegAlign program (DNASTAR version 7.1, Inc., Madison, WI, United States) and Simplot version 3.5.1 based on the complete genome and E2 sequence.

Techniques: Glycoproteomics