Ligand-induced folding of a two-component signaling receiver domain.

ABSTRACT: To survive and adapt to environmental changes, bacteria commonly use two-component signaling systems. Minimally, these pathways use histidine kinases (HKs) to detect environmental signals, harnessing these to control phosphorylation levels of receiver (REC) domains of downstream response regulators that convert this signal into physiological responses. Studies of several prototypical REC domains suggest that phosphorylation shifts these proteins between inactive and active structures that are globally similar and well-folded. However, it is unclear how globally these findings hold within REC domains in general, particularly when they are considered within full-length proteins. Here, we present EL_LovR, a full-length REC-only protein that is phosphorylated in response to blue light in the m

SUBMITTER: Ocasio VJ 

PROVIDER: S-EPMC4423417 | biostudies-literature | 2015 Feb

REPOSITORIES: biostudies-literature