3MPK

Crystal Structure of Bordetella pertussis BvgS periplasmic VFT2 domain

Summary for 3MPK

• Entry DOI: 10.2210/pdb3mpk/pdb
• Related: 3MPL
• Descriptor: Virulence sensor protein bvgS, GLYCEROL, ACETATE ION, ... (4 entities in total)
• Functional Keywords: venus flytrap, sensor domain, signaling protein
• Biological source: Bordetella pertussis
• Cellular location: Cell inner membrane; Multi-pass membrane protein (Probable): P16575
• Total number of polymer chains: 1
• Total formula weight: 29856.70

Authors

Herrou, J.,Bompard, C.,Wintjens, R.,Dupre, E.,Willery, E.,Villeret, V.,Locht, C.,Antoine, R.,Jacob-Dubuisson, F. (deposition date: 2010-04-27, release date: 2010-10-06, Last modification date: 2024-02-21)

Primary citation

Herrou, J.,Bompard, C.,Wintjens, R.,Dupre, E.,Willery, E.,Villeret, V.,Locht, C.,Antoine, R.,Jacob-Dubuisson, F.
Periplasmic domain of the sensor-kinase BvgS reveals a new paradigm for the Venus flytrap mechanism.
Proc.Natl.Acad.Sci.USA, 107:17351-17355, 2010

PubMed Abstract: Two-component sensory transduction systems control important bacterial programs. In Bordetella pertussis, expression of the virulence regulon is controlled by the unorthodox BvgAS two-component system. BvgS is the prototype of a family of sensor-kinases that harbor periplasmic domains homologous to bacterial solute-binding proteins. Although BvgAS is active under laboratory conditions, no activating signal has been identified, only negative modulators. Here we show that the second periplasmic domain of BvgS interacts with modulators and adopts a Venus flytrap (VFT) fold. X-ray crystallography reveals that the two lobes of VFT2 delimitate a ligand-binding cavity enclosing fortuitous ligands. Most substitutions of putative ligand-binding residues in the VFT2 cavity keep BvgS active, and alteration of the cavity's electrostatic potential affects responsiveness to modulation. The crystal structure of this VFT2 variant conferring constitutive kinase activity to BvgS shows a closed cavity with another nonspecific ligand. Thus, VFT2 is closed and active without a specific agonist ligand, in contrast to typical VFTs. Modulators are antagonists of VFT2 that interrupt signaling. BvgAS is active for most of the B. pertussis infectious cycle, consistent with the proposed mechanism.

PubMed: 20855615
DOI: 10.1073/pnas.1006267107

Experimental method

X-RAY DIFFRACTION (2.04 Å)