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. Author manuscript; available in PMC: 2011 Aug 1.
Published in final edited form as: Mol Microbiol. 2010 Jun 1;77(3):575–586. doi: 10.1111/j.1365-2958.2010.07231.x

Fig. 3.

Fig. 3

Signaling phenotypes and steady state concentrations of Aer mutant proteins. A. Amino acid substitutions that produced signal-on (above line), signal-on-biased (above line, circled), and signal-off (below line) phenotypes are mapped onto the secondary structural elements of the Aer PAS domain. Aer mutant proteins that were phenotypically rescued by Tar (see text) at low (*) or high (°) Aer expression levels are marked with an asterisk or superscripted circle, respectively. For secondary structure, cylinders represent helices, arrows represent β strands, and lines represent loops.

B. Steady state concentrations of the Aer mutant proteins relative to wild-type Aer when induced with 50 µM IPTG in the receptorless strain BT3388 (see Experimental Procedures). Mutant Aer proteins that were present at less than 50% (upper line) of wild-type Aer may be unstable. Degradation rates were determined for mutant proteins with steady state concentrations below 30% (lower line).