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| | <StructureSection load='4q0c' size='340' side='right'caption='[[4q0c]], [[Resolution|resolution]] 3.10Å' scene=''> | | <StructureSection load='4q0c' size='340' side='right'caption='[[4q0c]], [[Resolution|resolution]] 3.10Å' scene=''> |
| | == Structural highlights == | | == Structural highlights == |
| - | <table><tr><td colspan='2'>[[4q0c]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Borpe Borpe]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4Q0C OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4Q0C FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[4q0c]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Bordetella_pertussis_Tohama_I Bordetella pertussis Tohama I]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4Q0C OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4Q0C FirstGlance]. <br> |
| - | </td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">BP1877, bvgS, bvgS (BP1877) ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=257313 BORPE])</td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.1Å</td></tr> |
| - | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Histidine_kinase Histidine kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.13.3 2.7.13.3] </span></td></tr>
| + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4q0c FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4q0c OCA], [https://pdbe.org/4q0c PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4q0c RCSB], [https://www.ebi.ac.uk/pdbsum/4q0c PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4q0c ProSAT]</span></td></tr> |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4q0c FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4q0c OCA], [http://pdbe.org/4q0c PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4q0c RCSB], [http://www.ebi.ac.uk/pdbsum/4q0c PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4q0c ProSAT]</span></td></tr> | + | |
| | </table> | | </table> |
| | == Function == | | == Function == |
| - | [[http://www.uniprot.org/uniprot/BVGS_BORPE BVGS_BORPE]] Member of the two-component regulatory system BvgS/BvgA. Phosphorylates BvgA via a four-step phosphorelay in response to environmental signals. | + | [https://www.uniprot.org/uniprot/BVGS_BORPE BVGS_BORPE] Member of the two-component regulatory system BvgS/BvgA. Phosphorylates BvgA via a four-step phosphorelay in response to environmental signals. |
| | <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| | == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
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| | __TOC__ | | __TOC__ |
| | </StructureSection> | | </StructureSection> |
| - | [[Category: Borpe]] | + | [[Category: Bordetella pertussis Tohama I]] |
| - | [[Category: Histidine kinase]]
| + | |
| | [[Category: Large Structures]] | | [[Category: Large Structures]] |
| - | [[Category: Antoine, R]] | + | [[Category: Antoine R]] |
| - | [[Category: Crosson, S]] | + | [[Category: Crosson S]] |
| - | [[Category: Dupre, E]] | + | [[Category: Dupre E]] |
| - | [[Category: Herrou, J]] | + | [[Category: Herrou J]] |
| - | [[Category: Jacob-Dubuisson, F]] | + | [[Category: Jacob-Dubuisson F]] |
| - | [[Category: Lebedev, A]] | + | [[Category: Lebedev A]] |
| - | [[Category: Lensink, M F]] | + | [[Category: Lensink MF]] |
| - | [[Category: Locht, C]] | + | [[Category: Locht C]] |
| - | [[Category: Villeret, V]] | + | [[Category: Villeret V]] |
| - | [[Category: Wintjens, R]] | + | [[Category: Wintjens R]] |
| - | [[Category: Bacterial extracellular solute-binding protein]]
| + | |
| - | [[Category: Environmental signal]]
| + | |
| - | [[Category: Family 3]]
| + | |
| - | [[Category: Periplasmic binding protein]]
| + | |
| - | [[Category: Sensor domain]]
| + | |
| - | [[Category: Signal perception]]
| + | |
| - | [[Category: Transferase]]
| + | |
| - | [[Category: Venus fly trap]]
| + | |
| - | [[Category: Virulence regulation]]
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| Structural highlights
Function
BVGS_BORPE Member of the two-component regulatory system BvgS/BvgA. Phosphorylates BvgA via a four-step phosphorelay in response to environmental signals.
Publication Abstract from PubMed
Two-component systems (TCS) represent major signal-transduction pathways for adaptation to environmental conditions, and regulate many aspects of bacterial physiology. In the whooping cough agent Bordetella pertussis, the TCS BvgAS controls the virulence regulon, and is therefore critical for pathogenicity. BvgS is a prototypical TCS sensor-kinase with tandem periplasmic Venus flytrap (VFT) domains. VFT are bi-lobed domains that typically close around specific ligands using clamshell motions. We report the X-ray structure of the periplasmic moiety of BvgS, an intricate homodimer with a novel architecture. By combining site-directed mutagenesis, functional analyses and molecular modeling, we show that the conformation of the periplasmic moiety determines the state of BvgS activity. The intertwined structure of the periplasmic portion and the different conformation and dynamics of its mobile, membrane-distal VFT1 domains, and closed, membrane-proximal VFT2 domains, exert a conformational strain onto the transmembrane helices, which sets the cytoplasmic moiety in a kinase-on state by default corresponding to the virulent phase of the bacterium. Signaling the presence of negative signals perceived by the periplasmic domains implies a shift of BvgS to a distinct state of conformation and activity, corresponding to the avirulent phase. The response to negative modulation depends on the integrity of the periplasmic dimer, indicating that the shift to the kinase-off state implies a concerted conformational transition. This work lays the bases to understand virulence regulation in Bordetella. As homologous sensor-kinases control virulence features of diverse bacterial pathogens, the BvgS structure and mechanism may pave the way for new modes of targeted therapeutic interventions.
Virulence Regulation with Venus Flytrap Domains: Structure and Function of the Periplasmic Moiety of the Sensor-Kinase BvgS.,Dupre E, Herrou J, Lensink MF, Wintjens R, Vagin A, Lebedev A, Crosson S, Villeret V, Locht C, Antoine R, Jacob-Dubuisson F PLoS Pathog. 2015 Mar 4;11(3):e1004700. doi: 10.1371/journal.ppat.1004700., eCollection 2015 Mar. PMID:25738876[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Dupre E, Herrou J, Lensink MF, Wintjens R, Vagin A, Lebedev A, Crosson S, Villeret V, Locht C, Antoine R, Jacob-Dubuisson F. Virulence Regulation with Venus Flytrap Domains: Structure and Function of the Periplasmic Moiety of the Sensor-Kinase BvgS. PLoS Pathog. 2015 Mar 4;11(3):e1004700. doi: 10.1371/journal.ppat.1004700., eCollection 2015 Mar. PMID:25738876 doi:http://dx.doi.org/10.1371/journal.ppat.1004700
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