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. 2014 Sep;196(17):3179–3190. doi: 10.1128/JB.01842-14

TABLE 2.

Summary of RegA mutant proteins generated from the receiver domain and linker domain indicating RegA-CbbR (DNA) interactions (using probe-0) and DNA binding function manifested by the ability to bind probe-1234

RegA protein CbbR interaction (probe-0)a DNA binding
Probe-1234b Lowest [RegA] (nM)c
wt + +++ 40
Receiver domain
    D20A/D21A + 160
    R27L + ++ 40
    M32K No binding
    R35L + ++ 40
    K49E ++ 40
    P57A ++ 40
    D63A(-P) + +++ 40
    E67K + ++ 40
    R79G + 40
    D84A + +++ 40
    T91A + +++ 40
    A97S + +++ 40
    D109A + +++ 40
    K113M + +++ 40
Linker
    P134A + +++ 40
a

For CbbR interaction, + denotes interaction and − denotes no interaction.

b

For DNA binding, +++ denotes RegA/promoter complex size comparable to wild-type RegA size, ++ denotes complex size reduced relative to wild-type RegA size, + denotes severe reduction of complex size relative to wild-type RegA size, and − denotes no DNA binding relative to wild-type RegA binding.

c

Lowest concentration of RegA that bound probe-1234.