6sft
From Proteopedia
(Difference between revisions)
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<StructureSection load='6sft' size='340' side='right'caption='[[6sft]]' scene=''> | <StructureSection load='6sft' size='340' side='right'caption='[[6sft]]' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'> | + | <table><tr><td colspan='2'>Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6SFT OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6SFT FirstGlance]. <br> |
- | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=C2E:9,9-[(2R,3R,3aS,5S,7aR,9R,10R,10aS,12S,14aR)-3,5,10,12-tetrahydroxy-5,12-dioxidooctahydro-2H,7H-difuro[3,2-d 3,2-j][1,3,7,9,2,8]tetraoxadiphosphacyclododecine-2,9-diyl]bis(2-amino-1,9-dihydro-6H-purin-6-one)'>C2E</scene></td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr> |
+ | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=C2E:9,9-[(2R,3R,3aS,5S,7aR,9R,10R,10aS,12S,14aR)-3,5,10,12-tetrahydroxy-5,12-dioxidooctahydro-2H,7H-difuro[3,2-d 3,2-j][1,3,7,9,2,8]tetraoxadiphosphacyclododecine-2,9-diyl]bis(2-amino-1,9-dihydro-6H-purin-6-one)'>C2E</scene></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=6sft FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6sft OCA], [https://pdbe.org/6sft PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6sft RCSB], [https://www.ebi.ac.uk/pdbsum/6sft PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6sft ProSAT]</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=6sft FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6sft OCA], [https://pdbe.org/6sft PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6sft RCSB], [https://www.ebi.ac.uk/pdbsum/6sft PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6sft ProSAT]</span></td></tr> | ||
</table> | </table> | ||
- | == Function == | ||
- | [https://www.uniprot.org/uniprot/A0A0H3CCM2_CAUVN A0A0H3CCM2_CAUVN] | ||
- | <div style="background-color:#fffaf0;"> | ||
- | == Publication Abstract from PubMed == | ||
- | The bacterial second messenger cyclic diguanylate (c-di-GMP) regulates a wide range of cellular functions from biofilm formation to growth and survival. Targeting a second-messenger network is challenging because the system involves a multitude of components with often overlapping functions. Here, we present a strategy to intercept c-di-GMP signaling pathways by directly targeting the second messenger. For this, we developed a c-di-GMP-sequestering peptide (CSP) that was derived from a CheY-like c-di-GMP effector protein. CSP binds c-di-GMP with submicromolar affinity. The elucidation of the CSPc-di-GMP complex structure by NMR identified a linear c-di-GMP-binding motif, in which a self-intercalated c-di-GMP dimer is tightly bound by a network of H bonds and pi-stacking interactions involving arginine and aromatic residues. Structure-based mutagenesis yielded a variant with considerably higher, low-nanomolar affinity, which subsequently was shortened to 19 residues with almost uncompromised affinity. We demonstrate that endogenously expressed CSP intercepts c-di-GMP signaling and effectively inhibits biofilm formation in Pseudomonas aeruginosa, the most widely used model for serious biofilm-associated medical implications. | ||
- | |||
- | Intercepting second-messenger signaling by rationally designed peptides sequestering c-di-GMP.,Hee CS, Habazettl J, Schmutz C, Schirmer T, Jenal U, Grzesiek S Proc Natl Acad Sci U S A. 2020 Jul 21;117(29):17211-17220. doi:, 10.1073/pnas.2001232117. Epub 2020 Jul 1. PMID:32611811<ref>PMID:32611811</ref> | ||
- | |||
- | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
- | </div> | ||
- | <div class="pdbe-citations 6sft" style="background-color:#fffaf0;"></div> | ||
- | == References == | ||
- | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
- | [[Category: Caulobacter vibrioides NA1000]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Grzesiek S]] | [[Category: Grzesiek S]] |
Current revision
Solution structure of protein ARR_CleD in complex with c-di-GMP
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