5htl: Difference between revisions

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==Structure of MshE with cdg==
==Structure of MshE with cdg==
<StructureSection load='5htl' size='340' side='right' caption='[[5htl]], [[Resolution|resolution]] 1.37&Aring;' scene=''>
<StructureSection load='5htl' size='340' side='right'caption='[[5htl]], [[Resolution|resolution]] 1.37&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[5htl]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5HTL OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5HTL FirstGlance]. <br>
<table><tr><td colspan='2'>[[5htl]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Vibrio_cholerae Vibrio cholerae]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5HTL OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5HTL FirstGlance]. <br>
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><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">X-ray diffraction, [[Resolution|Resolution]] 1.371&#8491;</td></tr>
<tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=MSE:SELENOMETHIONINE'>MSE</scene></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>, <scene name='pdbligand=MSE:SELENOMETHIONINE'>MSE</scene></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=5htl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5htl OCA], [http://pdbe.org/5htl PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5htl RCSB], [http://www.ebi.ac.uk/pdbsum/5htl PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5htl 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=5htl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5htl OCA], [https://pdbe.org/5htl PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5htl RCSB], [https://www.ebi.ac.uk/pdbsum/5htl PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5htl ProSAT]</span></td></tr>
</table>
</table>
== Function ==
[https://www.uniprot.org/uniprot/Q9KUV7_VIBCH Q9KUV7_VIBCH]
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
C-di-GMP is a bacterial second messenger regulating various cellular functions. Many bacteria contain c-di-GMP-metabolizing enzymes but lack known c-di-GMP receptors. Recently, two MshE-type ATPases associated with bacterial type II secretion system and type IV pilus formation were shown to specifically bind c-di-GMP. Here we report crystal structure of the MshE N-terminal domain (MshEN1-145) from Vibrio cholerae in complex with c-di-GMP at a 1.37 A resolution. This structure reveals a unique c-di-GMP-binding mode, featuring a tandem array of two highly conserved binding motifs, each comprising a 24-residue sequence RLGxx(L/V/I)(L/V/I)xxG(L/V/I)(L/V/I)xxxxLxxxLxxQ that binds half of the c-di-GMP molecule, primarily through hydrophobic interactions. Mutating these highly conserved residues markedly reduces c-di-GMP binding and biofilm formation by V. cholerae. This c-di-GMP-binding motif is present in diverse bacterial proteins exhibiting binding affinities ranging from 0.5 muM to as low as 14 nM. The MshEN domain contains the longest nucleotide-binding motif reported to date.
Nucleotide binding by the widespread high-affinity cyclic di-GMP receptor MshEN domain.,Wang YC, Chin KH, Tu ZL, He J, Jones CJ, Sanchez DZ, Yildiz FH, Galperin MY, Chou SH Nat Commun. 2016 Aug 31;7:12481. doi: 10.1038/ncomms12481. PMID:27578558<ref>PMID:27578558</ref>
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 5htl" style="background-color:#fffaf0;"></div>
== References ==
<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Chin, K H]]
[[Category: Large Structures]]
[[Category: Wang, Y C]]
[[Category: Vibrio cholerae]]
[[Category: Biosynthetic protein]]
[[Category: Chin KH]]
[[Category: C-di-gmp]]
[[Category: Wang YC]]
[[Category: Mshe]]

Latest revision as of 10:53, 16 August 2023

Structure of MshE with cdg

5htl, resolution 1.37Å

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