View source for 9rpt


==Cryo-EM structure of the open state of Shigella flexneri LptDE bound by the RBP of Oekolampad phage==
<StructureSection load='9rpt' size='340' side='right'caption='[[9rpt]], [[Resolution|resolution]] 2.81&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[9rpt]] is a 3 chain structure with sequence from [https://en.wikipedia.org/wiki/Escherichia_phage_Oekolampad Escherichia phage Oekolampad] and [https://en.wikipedia.org/wiki/Shigella_flexneri Shigella flexneri]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=9RPT OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9RPT FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.81&#8491;</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=9rpt FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9rpt OCA], [https://pdbe.org/9rpt PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9rpt RCSB], [https://www.ebi.ac.uk/pdbsum/9rpt PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9rpt ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/LPTD_SHIFL LPTD_SHIFL] Together with LptE, is involved in the assembly of lipopolysaccharide (LPS) at the surface of the outer membrane (By similarity).
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== Publication Abstract from PubMed ==
Bacteriophages are bacterial viruses that provide alternatives to small-molecule drugs to combat infections by antibiotic-resistant bacteria. To infect a bacterial host, a phage needs to bind to the bacterial surface via receptor binding proteins (RBPs), which are critical for determining host specificity. For functionally important receptors, the RBP-receptor interaction could be exploited via phage steering, where emerging bacterial resistance due to receptor modification could make bacteria less fit or virulent. Despite this, relatively little is known about RBP-receptor interactions. Here, we build on the recent discovery of coliphages that have the outer membrane (OM) lipopolysaccharide translocon LptDE as their terminal receptor and show via cryogenic electron microscopy that, surprisingly, the RBP of the small siphophage Oekolampad binds to a hitherto unobserved, open state of LptDE. The open lateral gate of LptD is occupied by a beta-strand peptide originating from the degraded N-terminal jellyroll domain of LptD, suggesting the possibility of LptD inhibition via peptidomimetics. A structure of LptDE in complex with the superinfection exclusion (SE) protein Rtp45 of the Oekolampad-related phage Rtp shows a mechanism of SE where Rtp45-induced conformational changes in LptD resulting from steric clashes preclude RBP binding. Finally, analysis of spontaneous Oekolampad-resistant Escherichia coli mutants identifies mutations in LptD that abolish the LptDE-RBP interaction in vitro. SDS-EDTA sensitivity assays of the mutants show no major OM defects, consistent with largely preserved LptDE function, and suggesting that phage steering via LptDE might be challenging.

Small siphophage binding to an open state of the LptDE outer membrane lipopolysaccharide translocon.,Dunbar E, Clark R, Basle A, Allyjaun S, Newman H, Hubbard J, Khalid S, van den Berg B Proc Natl Acad Sci U S A. 2025 Dec 2;122(48):e2516650122. doi: , 10.1073/pnas.2516650122. Epub 2025 Nov 26. PMID:41296721<ref>PMID:41296721</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Escherichia phage Oekolampad]]
[[Category: Large Structures]]
[[Category: Shigella flexneri]]
[[Category: Basle A]]
[[Category: Dunbar E]]
[[Category: Van den Berg B]]