7nhs

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==Wzc K540M C8==
==Wzc K540M C8==
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<StructureSection load='7nhs' size='340' side='right'caption='[[7nhs]]' scene=''>
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<StructureSection load='7nhs' size='340' side='right'caption='[[7nhs]], [[Resolution|resolution]] 2.30&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7NHS OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7NHS FirstGlance]. <br>
<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7NHS OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7NHS FirstGlance]. <br>
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</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=7nhs FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7nhs OCA], [https://pdbe.org/7nhs PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7nhs RCSB], [https://www.ebi.ac.uk/pdbsum/7nhs PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7nhs ProSAT]</span></td></tr>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.3&#8491;</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=7nhs FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7nhs OCA], [https://pdbe.org/7nhs PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7nhs RCSB], [https://www.ebi.ac.uk/pdbsum/7nhs PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7nhs ProSAT]</span></td></tr>
</table>
</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Bacterial extracellular polysaccharides (EPSs) play critical roles in virulence. Many bacteria assemble EPSs via a multi-protein "Wzx-Wzy" system, involving glycan polymerization at the outer face of the cytoplasmic/inner membrane. Gram-negative species couple polymerization with translocation across the periplasm and outer membrane and the master regulator of the system is the tyrosine autokinase, Wzc. This near atomic cryo-EM structure of dephosphorylated Wzc from E. coli shows an octameric assembly with a large central cavity formed by transmembrane helices. The tyrosine autokinase domain forms the cytoplasm region, while the periplasmic region contains small folded motifs and helical bundles. The helical bundles are essential for function, most likely through interaction with the outer membrane translocon, Wza. Autophosphorylation of the tyrosine-rich C-terminus of Wzc results in disassembly of the octamer into multiply phosphorylated monomers. We propose that the cycling between phosphorylated monomer and dephosphorylated octamer regulates glycan polymerization and translocation.
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The molecular basis of regulation of bacterial capsule assembly by Wzc.,Yang Y, Liu J, Clarke BR, Seidel L, Bolla JR, Ward PN, Zhang P, Robinson CV, Whitfield C, Naismith JH Nat Commun. 2021 Jul 16;12(1):4349. doi: 10.1038/s41467-021-24652-1. PMID:34272394<ref>PMID:34272394</ref>
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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</div>
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<div class="pdbe-citations 7nhs" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>

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Wzc K540M C8

PDB ID 7nhs

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