|
|
Line 3: |
Line 3: |
| <StructureSection load='6dk8' size='340' side='right'caption='[[6dk8]], [[Resolution|resolution]] 3.80Å' scene=''> | | <StructureSection load='6dk8' size='340' side='right'caption='[[6dk8]], [[Resolution|resolution]] 3.80Å' scene=''> |
| == Structural highlights == | | == Structural highlights == |
- | <table><tr><td colspan='2'>[[6dk8]] is a 8 chain structure with sequence from [http://en.wikipedia.org/wiki/"bacillus_aeruginosus"_(schroeter_1872)_trevisan_1885 "bacillus aeruginosus" (schroeter 1872) trevisan 1885]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6DK8 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6DK8 FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[6dk8]] is a 8 chain structure with sequence from [https://en.wikipedia.org/wiki/Pseudomonas_aeruginosa Pseudomonas aeruginosa]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6DK8 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6DK8 FirstGlance]. <br> |
- | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=NI:NICKEL+(II)+ION'>NI</scene></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]] 3.8Å</td></tr> |
- | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[6dk7|6dk7]]</td></tr>
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=NI:NICKEL+(II)+ION'>NI</scene></td></tr> |
- | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">retS, PA4856 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=287 "Bacillus aeruginosus" (Schroeter 1872) Trevisan 1885])</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=6dk8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6dk8 OCA], [https://pdbe.org/6dk8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6dk8 RCSB], [https://www.ebi.ac.uk/pdbsum/6dk8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6dk8 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=6dk8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6dk8 OCA], [http://pdbe.org/6dk8 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6dk8 RCSB], [http://www.ebi.ac.uk/pdbsum/6dk8 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6dk8 ProSAT]</span></td></tr> | + | |
| </table> | | </table> |
| + | == Function == |
| + | [https://www.uniprot.org/uniprot/Q9HUV7_PSEAE Q9HUV7_PSEAE] |
| <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
Line 23: |
Line 24: |
| </StructureSection> | | </StructureSection> |
| [[Category: Large Structures]] | | [[Category: Large Structures]] |
- | [[Category: Mancl, J M]] | + | [[Category: Pseudomonas aeruginosa]] |
- | [[Category: Schubot, F D]] | + | [[Category: Mancl JM]] |
- | [[Category: Histidine kinase]] | + | [[Category: Schubot FD]] |
- | [[Category: Inhibitor]]
| + | |
- | [[Category: Signaling protein]]
| + | |
| Structural highlights
Function
Q9HUV7_PSEAE
Publication Abstract from PubMed
Recent paradigm shifting discoveries have demonstrated that bacterial signaling kinases engage in unexpected regulatory crosstalk, yet the underlying molecular mechanisms remain largely uncharacterized. The Pseudomonas aeruginosa RetS/GacS system constitutes an ideal model for studying these mechanisms. The in-depth analysis of the kinase region of RetS and RetS/GacS interactions presented here refutes a longstanding model, which posited the formation of a catalytically inactive RetS/GacS heterodimer. Crystallographic studies uncovered structurally dynamic features within the RetS kinase region, suggesting that RetS uses the reversible unfolding of a helix, or helix cracking, to control interactions with GacS. The pivotal importance of this helical region for regulating GacS and, by extension, Pseudomonas aeruginosa virulence, was corroborated via in vivo assays. The implications of this work extend beyond the RetS/GacS system because the helix cracking occurs right next to a highly conserved catalytic residue histidine-424, suggesting this model could represent an emergent archetype for histidine kinase regulation.
Helix Cracking Regulates the Critical Interaction between RetS and GacS in Pseudomonas aeruginosa.,Mancl JM, Ray WK, Helm RF, Schubot FD Structure. 2019 Mar 5. pii: S0969-2126(19)30050-4. doi:, 10.1016/j.str.2019.02.006. PMID:30879888[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Mancl JM, Ray WK, Helm RF, Schubot FD. Helix Cracking Regulates the Critical Interaction between RetS and GacS in Pseudomonas aeruginosa. Structure. 2019 Mar 5. pii: S0969-2126(19)30050-4. doi:, 10.1016/j.str.2019.02.006. PMID:30879888 doi:http://dx.doi.org/10.1016/j.str.2019.02.006
|