, 2010). These complex structures are composed of several protein subunits, all of which require tight control of their synthesis, export, folding

and assembly process for final functional structure formation (Ruiz & Silhavy, 2005). Stresses that interfere with these processes activate the Cpx-envelope stress system (Fig. 1; reviewed in MacRitchie et al., 2008), which responds not only by regulating the expression of folding factors and proteases in the envelope to deal with the misfolded proteins but also by inhibiting the expression of the surface PI3K Inhibitor Library structures (Dorel et al., 2006; Vogt et al., 2010). Because these surface structures include important virulence determinants such as adhesins and secretion systems, the Cpx system contributes to virulence in several Gram-negative species (Raivio, 2005; Rowley et al., 2006). The Cpx system belongs to the group of two-component signal transduction systems (TCSs) and is made up of the senor kinase (SK) CpxA, the

response regulator (RR) CpxR and the periplasmic accessory inhibitor CpxP (Fig. 1; Ruiz & Silhavy, 2005; Buelow & Raivio, 2010), which provides response to additional stimuli (Buelow & Raivio, 2010; Heermann & Jung, 2010; Krell et al., 2010). Three phosphotransfer reactions are involved in controlling the functional state of the Cpx-TCS: (1) the autophosphorylation Target Selective Inhibitor Library datasheet of a conserved histidine of the SK CpxA, (2) the transphosphorylation of a conserved aspartate of the RR CpxR and (3) the dephosphorylation of phosphorylated RR to return the system back to the prestimulated resting state (Gao & Stock, 2009). Importantly, the balance between phosphorylated and dephosphorylated RRs is crucial not only for the initiation of a specific genetic response to the external stimulus but also for its duration

(Stock et al., 2000; Dorel et al., 2006). It has been suggested that all inducing cues involve misfolded envelope proteins as the actual common stimulus for the Cpx-TCS (Raivio & Silhavy, 2001) and/or dissociation of the inhibitory CpxP from CpxA (Rowley et al., 2006), as well as signal specificity for the Cpx response (DiGiuseppe & Silhavy, 2003; Hunke & Betton, 2003; Ruiz & Silhavy, 2005). However, where and how the independent Demeclocycline entry points for this signalling system take place has to be addressed. The pivotal factor of the Cpx-TCS is CpxA with its central function as a sensor kinase. Sequence alignments revealed that CpxA belongs to class I SK (Grebe & Stock, 1998; Dutta et al., 1999), typically consisting of two transmembrane domains (TMDs) integrating a large periplasmic domain and a cytoplasmic, highly conserved kinase core that acts as a transmitter domain (Fig. 2). The cytosolic domain includes a HAMP domain, which links the second TMD of CpxA with its kinase core (Appleman et al.