6d0i

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'''Unreleased structure'''
 
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The entry 6d0i is ON HOLD until Paper Publication
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==ParT: Prs ADP-ribosylating toxin bound to cognate antitoxin ParS. L48M ParT, SeMet-substituted complex.==
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<StructureSection load='6d0i' size='340' side='right' caption='[[6d0i]], [[Resolution|resolution]] 1.55&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6d0i]] is a 4 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6D0I OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6D0I FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene></td></tr>
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<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>
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<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=6d0i FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6d0i OCA], [http://pdbe.org/6d0i PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6d0i RCSB], [http://www.ebi.ac.uk/pdbsum/6d0i PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6d0i ProSAT]</span></td></tr>
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</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Toxin-antitoxin (TA) systems interfere with essential cellular processes and are implicated in bacterial lifestyle adaptations such as persistence and the biofilm formation. Here, we present structural, biochemical, and functional data on an uncharacterized TA system, the COG5654-COG5642 pair. Bioinformatic analysis showed that this TA pair is found in 2,942 of the 16,286 distinct bacterial species in the RefSeq database. We solved a structure of the toxin bound to a fragment of the antitoxin to 1.50 A. This structure suggested that the toxin is a mono-ADP-ribosyltransferase (mART). The toxin specifically modifies phosphoribosyl pyrophosphate synthetase (Prs), an essential enzyme in nucleotide biosynthesis conserved in all organisms. We propose renaming the toxin ParT for Prs ADP-ribosylating toxin and ParS for the cognate antitoxin. ParT is a unique example of an intracellular protein mART in bacteria and is the smallest known mART. This work demonstrates that TA systems can induce bacteriostasis through interference with nucleotide biosynthesis.
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Authors:
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ParST is a widespread toxin-antitoxin module that targets nucleotide metabolism.,Piscotta FJ, Jeffrey PD, Link AJ Proc Natl Acad Sci U S A. 2018 Dec 31. pii: 1814633116. doi:, 10.1073/pnas.1814633116. PMID:30598453<ref>PMID:30598453</ref>
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Description:
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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<div class="pdbe-citations 6d0i" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Jeffrey, P D]]
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[[Category: Link, A J]]
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[[Category: Piscotta, F J]]
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[[Category: Adp-ribosyltransferase]]
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[[Category: Parst]]
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[[Category: Toxin]]
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[[Category: Toxin-antitoxin complex]]

Revision as of 06:34, 9 January 2019

ParT: Prs ADP-ribosylating toxin bound to cognate antitoxin ParS. L48M ParT, SeMet-substituted complex.

6d0i, resolution 1.55Å

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