Figure 10From: Characterization of the GXXXG motif in the first transmembrane segment of Japanese encephalitis virus precursor membrane (prM) proteinCharacterization of the GXXXG motif of the TM1 region of the prM protein by glycine-substitution mutagenesis. Glycine residues at 142 and 146 were substituted by alanine, leucine, or valine to investigate the relationship between the GXXXG motif and the prM-E binding affinity.Back to article page