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. 2022 May 28;117(6):1464–1478. doi: 10.1111/mmi.14921

TABLE 1.

Transcription activation and binding capabilities of native and modified SHPs

Peptide a Transcription activation b (Miller units/109 cells) Binding affinities (KD c in μM)
C13 (WT) 215 ± 5 6.6 ± 0.3
S14A 105 ± 5 8.1 ± 0.9
E15A 107 ± 2.5 3.3 ± 0.1
W16A 7.5 ± 2.5 50.0 ± 3.6
V17A 6 ± 1 9.7 ± 0.6
I18A 7.5 ± 1.5 >100
V19A 215 ± 5 4.0 ± 0.8
I20A 8.5 ± 0.5 23.54
P21A 7.5 ± 2.5 1.7 ± 0.1
F22A 90 ± 10 7.1 ± 0.4
L23A 95 ± 5 4.3 ± 0.2
T24A 175 ± 5 3.3 ± 0.1
N25A 185 ± 5 3.3 ± 0.2
L26A 182 ± 2.5 3.4 ± 0.3
a

WT C13 or modified peptides were used. The numbers show the position of alanine replacement within the full‐length Shp144.

b

Mean ± SEM of three independent experiments.

c

Dissociation constant between the Rgg144 and its ligand SHP144.