6sft

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Current revision (06:08, 19 June 2024) (edit) (undo)
 
Line 3: Line 3:
<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'>[[6sft]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Caulobacter_vibrioides_NA1000 Caulobacter vibrioides NA1000]. 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>
+
<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&reg;/PubMed&reg;, 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

PDB ID 6sft

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools