9kn2

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Current revision (05:53, 1 October 2025) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 9kn2 is ON HOLD until Paper Publication
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==Crystallization of zinc metalloproteinase PepO from Porphyromonas gingivalis==
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<StructureSection load='9kn2' size='340' side='right'caption='[[9kn2]], [[Resolution|resolution]] 2.04&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[9kn2]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Porphyromonas_gingivalis_W83 Porphyromonas gingivalis W83]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=9KN2 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9KN2 FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.04&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=RDF:N-ALPHA-L-RHAMNOPYRANOSYLOXY(HYDROXYPHOSPHINYL)-L-LEUCYL-L-TRYPTOPHAN'>RDF</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9kn2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9kn2 OCA], [https://pdbe.org/9kn2 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9kn2 RCSB], [https://www.ebi.ac.uk/pdbsum/9kn2 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9kn2 ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/Q7MXL5_PORGI Q7MXL5_PORGI]
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The pathogen Porphyromonas gingivalis contributes to the pathogenesis of periodontitis and other systemic diseases. The zinc-dependent metallopeptidase PepO is a virulence factor that plays a crucial role in the adhesion and invasion of Porphyromonas gingivalis to human cells. Here, we solved the 2.04 A crystal structure of wild-type PepO in complex with the inhibitor phosphoramidon. The active-site pocket of PepO appears to exhibit an increased hydrophobicity and a more pronounced negative charge, highlighting distinct structural features compared to its homologs. In addition to phosphoramidon, several zinc metallopeptidase inhibitors, including thiorphan, omapatrilat, and sacubitrilat, exhibited varying degrees of inhibition on PepO enzymatic activity. Notably, the recombinant PepO showed distinct binding profiles to human fibrinogen, a characteristic that likely contributes to its role as virulence factors. These findings provide significant insights into the structural and functional mechanisms of PepO, offering a platform for the rational design of targeted inhibitors against the periodontal pathogen P. gingivalis.
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Authors: Feng, C.Y., Feng, C.Y.
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Structural and biochemical characterization of a zinc metallopeptidase from Porphyromonas gingivalis.,Feng C, Yu W, Jiang Y, Xia R Biochem Biophys Res Commun. 2025 Jan;744:151201. doi: 10.1016/j.bbrc.2024.151201. , Epub 2024 Dec 18. PMID:39709774<ref>PMID:39709774</ref>
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Description: Crystallization of zinc metalloproteinase PepO from Porphyromonas gingivalis
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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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[[Category: Feng, C.Y]]
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<div class="pdbe-citations 9kn2" 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: Large Structures]]
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[[Category: Porphyromonas gingivalis W83]]
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[[Category: Feng CY]]

Current revision

Crystallization of zinc metalloproteinase PepO from Porphyromonas gingivalis

PDB ID 9kn2

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