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5tz8

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==Crystal structure of S. aureus TarS==
==Crystal structure of S. aureus TarS==
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<StructureSection load='5tz8' size='340' side='right' caption='[[5tz8]], [[Resolution|resolution]] 4.00&Aring;' scene=''>
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<StructureSection load='5tz8' size='340' side='right'caption='[[5tz8]], [[Resolution|resolution]] 4.00&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>[[5tz8]] is a 3 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5TZ8 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5TZ8 FirstGlance]. <br>
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<table><tr><td colspan='2'>[[5tz8]] is a 3 chain structure with sequence from [https://en.wikipedia.org/wiki/Staphylococcus_aureus Staphylococcus aureus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5TZ8 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5TZ8 FirstGlance]. <br>
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</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5tzk|5tzk]], [[5tze|5tze]], [[5tzj|5tzj]], [[5tzi|5tzi]], [[5u02|5u02]]</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">X-ray diffraction, [[Resolution|Resolution]] 4&#8491;</td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5tz8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5tz8 OCA], [http://pdbe.org/5tz8 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5tz8 RCSB], [http://www.ebi.ac.uk/pdbsum/5tz8 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5tz8 ProSAT]</span></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=5tz8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5tz8 OCA], [https://pdbe.org/5tz8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5tz8 RCSB], [https://www.ebi.ac.uk/pdbsum/5tz8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5tz8 ProSAT]</span></td></tr>
</table>
</table>
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<div style="background-color:#fffaf0;">
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== Function ==
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== Publication Abstract from PubMed ==
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[https://www.uniprot.org/uniprot/TARS_STAAM TARS_STAAM] Attaches beta-O-GlcNAc (beta-O-N-acetyl-D-glucosamine) residues to the C4 position of poly(RboP)-wall teichoic acids (WTAs). Mediates beta-lactam resistance in methicillin resistant Staphylococcus aureus (MRSA) strains.<ref>PMID:27973583</ref>
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In recent years, there has been a growing interest in teichoic acids as targets for antibiotic drug design against major clinical pathogens such as Staphylococcus aureus, reflecting the disquieting increase in antibiotic resistance and the historical success of bacterial cell wall components as drug targets. It is now becoming clear that beta-O-GlcNAcylation of S. aureus wall teichoic acids plays a major role in both pathogenicity and antibiotic resistance. Here we present the first structure of S. aureus TarS, the enzyme responsible for polyribitol phosphate beta-O-GlcNAcylation. Using a divide and conquer strategy, we obtained crystal structures of various TarS constructs, mapping high resolution overlapping N-terminal and C-terminal structures onto a lower resolution full-length structure that resulted in a high resolution view of the entire enzyme. Using the N-terminal structure that encapsulates the catalytic domain, we furthermore captured several snapshots of TarS, including the native structure, the UDP-GlcNAc donor complex, and the UDP product complex. These structures along with structure-guided mutants allowed us to elucidate various catalytic features and identify key active site residues and catalytic loop rearrangements that provide a valuable platform for anti-MRSA drug design. We furthermore observed for the first time the presence of a trimerization domain composed of stacked carbohydrate binding modules, commonly observed in starch active enzymes, but adapted here for a poly sugar-phosphate glycosyltransferase.
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Structure and Mechanism of Staphylococcus aureus TarS, the Wall Teichoic Acid beta-glycosyltransferase Involved in Methicillin Resistance.,Sobhanifar S, Worrall LJ, King DT, Wasney GA, Baumann L, Gale RT, Nosella M, Brown ED, Withers SG, Strynadka NC PLoS Pathog. 2016 Dec 14;12(12):e1006067. doi: 10.1371/journal.ppat.1006067., eCollection 2016 Dec. PMID:27973583<ref>PMID:27973583</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 5tz8" style="background-color:#fffaf0;"></div>
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== References ==
== References ==
<references/>
<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
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[[Category: King, D T]]
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[[Category: Large Structures]]
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[[Category: Sobhanifar, S]]
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[[Category: Staphylococcus aureus]]
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[[Category: Strynadka, N C]]
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[[Category: King DT]]
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[[Category: Worrall, L J]]
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[[Category: Sobhanifar S]]
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[[Category: Glycosyltransferase]]
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[[Category: Strynadka NC]]
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[[Category: Gt-a]]
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[[Category: Worrall LJ]]
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[[Category: Transferase]]
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[[Category: Wall teichoic acid]]
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Current revision

Crystal structure of S. aureus TarS

PDB ID 5tz8

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