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. 2000 Mar 1;19(5):831–842. doi: 10.1093/emboj/19.5.831

Table II. Residues involved in the MalT interaction patch as deduced by mutational screening of repressor-negative MalY mutants.

Plasmid β-galactosidase activitya
  before inductionb after inductionc
Wild-type 0.03 0.005
Null (vector) 2.17 2.68
T83A 1.29 0.03
T83Id 1.16 0.47
A84T 0.29 unstable
A84V 1.11 0.01
C181Rd 0.99 0.01
C181T 1.43 0.02
C181T, T244Y 0.26 unstable
E185G 1.16 0.02
A188T 0.92 0.002
D189G 0.58 0.001
I215Td 1.46 1.26
S218R 1.43 0.22
N219D 1.26 0.01
A221Vd 1.45 0.33

aSpecific β-galactosidase activity of the malK–lacZ fusion of strain EZ7 after growth overnight in minimal medium with glycerol as the carbon source. Specific activity is given in μmol substrate hydrolysed/min/mg protein.

bThe reduction of MalY-related repressor function is proportional to the value of β-galactosidase activity before induction with IPTG.

cInduction was with 100 μM IPTG.

dMutation that was obtained more than once.