View source for 6yze


==Zinc metalloprotease ProA from native source==
<StructureSection load='6yze' size='340' side='right'caption='[[6yze]], [[Resolution|resolution]] 2.18&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[6yze]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Legionella_pneumophila Legionella pneumophila]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6YZE OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6YZE FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.18&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ZN:ZINC+ION'>ZN</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=6yze FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6yze OCA], [https://pdbe.org/6yze PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6yze RCSB], [https://www.ebi.ac.uk/pdbsum/6yze PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6yze ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/PROA_LEGPN PROA_LEGPN] 
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
ProA is a secreted zinc metalloprotease of Legionella pneumophila causing lung damage in animal models of Legionnaires' disease. Here we demonstrate that ProA promotes infection of human lung tissue explants (HLTEs) and dissect the contribution to cell type specific replication and extracellular virulence mechanisms. For the first time, we reveal that co-incubation of HLTEs with purified ProA causes a significant increase of the alveolar septal thickness. This destruction of connective tissue fibers was further substantiated by collagen IV degradation assays. The moderate attenuation of a proA-negative mutant in A549 epithelial cells and THP-1 macrophages suggest that effects of ProA in tissue mainly result from extracellular activity. Correspondingly, ProA contributes to dissemination and serum resistance of the pathogen, which further expands the versatile substrate spectrum of this thermolysin-like protease. The crystal structure of ProA at 1.48 a resolution showed high congruence to pseudolysin of Pseudomonas aeruginosa, but revealed deviations in flexible loops, the substrate binding pocket S1 ' and the repertoire of cofactors, by which ProA can be distinguished from respective homologs. In sum, this work specified virulence features of ProA at different organizational levels by zooming in from histopathological effects in human lung tissue to atomic details of the protease substrate determination. This article is protected by copyright. All rights reserved.

Zinc metalloprotease ProA of Legionella pneumophila increases alveolar septal thickness in human lung tissue explants by collagen IV degradation.,Scheithauer L, Thiem S, Schmelz S, Dellmann A, Bussow K, Brouwer RMHJ, Unal CM, Blankenfeldt W, Steinert M Cell Microbiol. 2021 Jan 24:e13313. doi: 10.1111/cmi.13313. PMID:33491325<ref>PMID:33491325</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 6yze" style="background-color:#fffaf0;"></div>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Large Structures]]
[[Category: Legionella pneumophila]]
[[Category: Blankenfeldt W]]
[[Category: Schmelz S]]