4urn: Difference between revisions
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==Crystal Structure of Staph ParE 24kDa in complex with Novobiocin== | ==Crystal Structure of Staph ParE 24kDa in complex with Novobiocin== | ||
<StructureSection load='4urn' size='340' side='right' caption='[[4urn]], [[Resolution|resolution]] 2.30Å' scene=''> | <StructureSection load='4urn' size='340' side='right' caption='[[4urn]], [[Resolution|resolution]] 2.30Å' scene=''> | ||
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=NOV:NOVOBIOCIN'>NOV</scene></td></tr> | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=NOV:NOVOBIOCIN'>NOV</scene></td></tr> | ||
<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4url|4url]], [[4urm|4urm]], [[4uro|4uro]]</td></tr> | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4url|4url]], [[4urm|4urm]], [[4uro|4uro]]</td></tr> | ||
<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=4urn FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4urn OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4urn RCSB], [http://www.ebi.ac.uk/pdbsum/4urn PDBsum]</span></td></tr> | <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=4urn FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4urn OCA], [http://pdbe.org/4urn PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4urn RCSB], [http://www.ebi.ac.uk/pdbsum/4urn PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4urn ProSAT]</span></td></tr> | ||
</table> | </table> | ||
== Function == | == Function == | ||
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
</div> | </div> | ||
<div class="pdbe-citations 4urn" style="background-color:#fffaf0;"></div> | |||
==See Also== | |||
*[[Topoisomerase|Topoisomerase]] | |||
== References == | == References == | ||
<references/> | <references/> | ||
Revision as of 08:35, 5 August 2016
Crystal Structure of Staph ParE 24kDa in complex with NovobiocinCrystal Structure of Staph ParE 24kDa in complex with Novobiocin
Structural highlights
Function[X5EN43_STAAU] Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule (By similarity).[HAMAP-Rule:MF_00939] Publication Abstract from PubMedBacterial resistance to antibiotics continues to pose serious challenges as the discovery rate for new antibiotics fades. Kibdelomycin is one of the rare, novel, natural product antibiotics discovered recently that inhibits the bacterial DNA synthesis enzymes gyrase and topoisomerase IV. It is a broad-spectrum, Gram-positive antibiotic without cross-resistance to known gyrase inhibitors, including clinically effective quinolones. To understand its mechanism of action, binding mode, and lack of cross-resistance, we have co-crystallized kibdelomycin and novobiocin with the N-terminal domains of Staphylococcus aureus gyrase B (24 kDa) and topo IV (ParE, 24 and 43 kDa). Kibdelomycin shows a unique "dual-arm", U-shaped binding mode in both crystal structures. The pyrrolamide moiety in the lower part of kibdelomycin penetrates deeply into the ATP-binding site pocket, whereas the isopropyl-tetramic acid and sugar moiety of the upper part thoroughly engage in polar interactions with a surface patch of the protein. The isoproramic acid (1,3-dioxopyrrolidine) and a tetrahydropyran acetate group (Sugar A) make polar contact with a surface area consisting of helix alpha4 and the flexible loop connecting helices alpha3 and alpha4. The two arms are connected together by a rigid decalin linker that makes van del Waals contacts with the protein backbone. This "dual-arm", U-shaped, multicontact binding mode of kibdelomycin is unique and distinctively different from binding modes of other known gyrase inhibitors (e.g., coumarins and quinolones), which explains its lack of cross-resistance and low frequency of resistance. The crystal structures reported in this paper should enable design and discovery of analogues with better properties and antibacterial spectrum. Structures of Kibdelomycin Bound to Staphylococcus aureus GyrB and ParE Showed a Novel U-Shaped Binding Mode.,Lu J, Patel S, Sharma N, Soisson SM, Kishii R, Takei M, Fukuda Y, Lumb KJ, Singh SB ACS Chem Biol. 2014 Jul 3. PMID:24992706[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. See AlsoReferences
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