| Literature DB >> 18687869 |
Sigrun Rumpel1, Raghavendran Lakshmi, Stefan Becker, Markus Zweckstetter.
Abstract
The X-ray structure of the homodimeric chaperone CesT is the only structure among the type three secretion system (TTSS) chaperones that shows a domain swap. This swap has potential importance for the mechanism of effector translocation through a TTSS. Here we present two nuclear magnetic resonance strategies exploiting pre-existing structural models and residual dipolar couplings (RDCs), which reveal the unswapped 35.4-kDa dimer to be present in solution. Particularly efficient is the discrimination of a swapped and unswapped structural state performed simultaneously to automatic backbone assignment using only HN-RDCs and carbonyl backbone chemical shifts. This direct approach may prove to be generally useful to rapidly differentiate two structural models.Mesh:
Substances:
Year: 2008 PMID: 18687869 PMCID: PMC2578808 DOI: 10.1110/ps.036160.108
Source DB: PubMed Journal: Protein Sci ISSN: 0961-8368 Impact factor: 6.725