6apw
From Proteopedia
(Difference between revisions)
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<StructureSection load='6apw' size='340' side='right'caption='[[6apw]], [[Resolution|resolution]] 2.61Å' scene=''> | <StructureSection load='6apw' size='340' side='right'caption='[[6apw]], [[Resolution|resolution]] 2.61Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>[[6apw]] is a 1 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[6apw]] is a 1 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=6APW OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6APW FirstGlance]. <br> |
- | </td></tr><tr id=' | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.614Å</td></tr> |
- | <tr id=' | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=BTV:4-[(4-{5-[(3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentyl}-1H-1,2,3-triazol-1-yl)methyl]benzoic+acid'>BTV</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=6apw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6apw OCA], [https://pdbe.org/6apw PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6apw RCSB], [https://www.ebi.ac.uk/pdbsum/6apw PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6apw ProSAT]</span></td></tr> | |
- | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | |
</table> | </table> | ||
- | == Function == | ||
- | [[http://www.uniprot.org/uniprot/A0A181HT70_STAAU A0A181HT70_STAAU]] Acts both as a biotin--[acetyl-CoA-carboxylase] ligase and a repressor.[HAMAP-Rule:MF_00978] | ||
- | <div style="background-color:#fffaf0;"> | ||
- | == Publication Abstract from PubMed == | ||
- | We report the synthesis and evaluation of 5-halogenated-1,2,3-triazoles as inhibitors of biotin protein ligase from Staphylococcus aureus. The halogenated compounds exhibit significantly improved antibacterial activity over their nonhalogenated counterparts. Importantly, the 5-fluoro-1,2,3-triazole compound 4c displays antibacterial activity against S. aureus ATCC49775 with a minimum inhibitory concentration (MIC) of 8 mug/mL. | ||
- | |||
- | Halogenation of Biotin Protein Ligase Inhibitors Improves Whole Cell Activity against Staphylococcus aureus.,Paparella AS, Lee KJ, Hayes AJ, Feng J, Feng Z, Cini D, Deshmukh S, Booker GW, Wilce MCJ, Polyak SW, Abell AD ACS Infect Dis. 2017 Nov 16. doi: 10.1021/acsinfecdis.7b00134. PMID:29131575<ref>PMID:29131575</ref> | ||
- | |||
- | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
- | </div> | ||
- | <div class="pdbe-citations 6apw" style="background-color:#fffaf0;"></div> | ||
==See Also== | ==See Also== | ||
*[[Biotin Protein Ligase 3D structures|Biotin Protein Ligase 3D structures]] | *[[Biotin Protein Ligase 3D structures|Biotin Protein Ligase 3D structures]] | ||
- | == References == | ||
- | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
- | [[Category: | + | [[Category: Staphylococcus aureus]] |
- | [[Category: | + | [[Category: Cini DA]] |
- | [[Category: | + | [[Category: Wilce MCJ]] |
- | + | ||
- | + |
Current revision
Crystal structure of Staphylococcus aureus biotin protein ligase in complex with inhibitor
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