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8g01

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Current revision (12:38, 26 July 2023) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 8g01 is ON HOLD until Paper Publication
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==YES Complex - E. coli MraY, Protein E ID21, E. coli SlyD==
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<StructureSection load='8g01' size='340' side='right'caption='[[8g01]], [[Resolution|resolution]] 3.40&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8g01]] is a 6 chain structure with sequence from [https://en.wikipedia.org/wiki/Escherichia_coli_K-12 Escherichia coli K-12] and [https://en.wikipedia.org/wiki/Escherichia_phage_ID21 Escherichia phage ID21]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8G01 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8G01 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">Electron Microscopy, [[Resolution|Resolution]] 3.4&#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=8g01 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8g01 OCA], [https://pdbe.org/8g01 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8g01 RCSB], [https://www.ebi.ac.uk/pdbsum/8g01 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8g01 ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/MRAY_ECOLI MRAY_ECOLI] Catalyzes the initial step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan: transfers peptidoglycan precursor phospho-MurNAc-pentapeptide from UDP-MurNAc-pentapeptide onto the lipid carrier undecaprenyl phosphate, yielding undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide, known as lipid I.[HAMAP-Rule:MF_00038]<ref>PMID:1846850</ref> <ref>PMID:215212</ref>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The historically important phage PhiX174 kills its host bacteria by encoding a 91-residue protein antibiotic called protein E. Using single-particle electron cryo-microscopy, we demonstrate that protein E bridges two bacterial proteins to form the transmembrane YES complex [MraY, protein E, sensitivity to lysis D (SlyD)]. Protein E inhibits peptidoglycan biosynthesis by obstructing the MraY active site leading to loss of lipid I production. We experimentally validate this result for two different viral species, providing a clear model for bacterial lysis and unifying previous experimental data. Additionally, we characterize the Escherichia coli MraY structure-revealing features of this essential enzyme-and the structure of the chaperone SlyD bound to a protein. Our structures provide insights into the mechanism of phage-mediated lysis and for structure-based design of phage therapeutics.
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Authors:
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The mechanism of the phage-encoded protein antibiotic from PhiX174.,Orta AK, Riera N, Li YE, Tanaka S, Yun HG, Klaic L, Clemons WM Jr Science. 2023 Jul 14;381(6654):eadg9091. doi: 10.1126/science.adg9091. Epub 2023 , Jul 14. PMID:37440661<ref>PMID:37440661</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 8g01" 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: Escherichia coli K-12]]
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[[Category: Escherichia phage ID21]]
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[[Category: Large Structures]]
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[[Category: Clemons WM]]
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[[Category: Orta AK]]
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[[Category: Riera N]]

Current revision

YES Complex - E. coli MraY, Protein E ID21, E. coli SlyD

PDB ID 8g01

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