IraM remodels the RssB segmented helical linker to stabilize σ^s against degradation by ClpXP.

ABSTRACT: Upon Mg²⁺ starvation, a condition often associated with virulence, enterobacteria inhibit the ClpXP-dependent proteolysis of the master transcriptional regulator, σ^s, via IraM, a poorly understood antiadaptor that prevents RssB-dependent loading of σ^s onto ClpXP. This inhibition results in σ^s accumulation and expression of stress resistance genes. Here, we report on the structural analysis of RssB bound to IraM, which reveals that IraM induces two folding transitions within RssB, amplified via a segmented helical linker. These conformational changes result in an open, yet inhibited RssB structure in which IraM associates with both the C-terminal and N-terminal domains of RssB and prevents binding of σ^s to the 4-5-5 face of the N-termin

SUBMITTER: Brugger C 

PROVIDER: S-EPMC10844676 | biostudies-literature | 2024 Feb

REPOSITORIES: biostudies-literature