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. 2016 Feb 11;90(5):2264–2272. doi: 10.1128/JVI.02739-15

FIG 5.

FIG 5

The G672R mutation and the deletion of K883 in the cytoplasmic tail of gBB4.1 account for enhanced fusion activity. To test which changes in gBB4.1 are responsible for the higher fusion activity, mutations were introduced singly or in combinations into gBKa. Fusion activity in combination with gHKa was measured in cotransfected RK13 cells, and results from assays with gBB4.1 and gHKa were set as 100%. Given are mean values from three independent experiments with corresponding standard deviations.