3wyi

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'''Unreleased structure'''
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==Structure of S. aureus undecaprenyl diphosphate synthase==
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<StructureSection load='3wyi' size='340' side='right' caption='[[3wyi]], [[Resolution|resolution]] 2.00&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[3wyi]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3WYI OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3WYI FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene></td></tr>
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<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[3wyj|3wyj]]</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=3wyi FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3wyi OCA], [http://www.rcsb.org/pdb/explore.do?structureId=3wyi RCSB], [http://www.ebi.ac.uk/pdbsum/3wyi PDBsum]</span></td></tr>
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</table>
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== Function ==
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[[http://www.uniprot.org/uniprot/W8UYA6_STAAU W8UYA6_STAAU]] Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids.[HAMAP-Rule:MF_01139]
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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We report the results of an investigation of the activity of a series of amidine and bisamidine compounds against Staphylococcus aureus and Escherichia coli. The most active compounds bound to an AT-rich DNA dodecamer (CGCGAATTCGCG)2 and using DSC were found to increase the melting transition by up to 24 degrees C. Several compounds also inhibited undecaprenyl diphosphate synthase (UPPS) with IC50 values of 100-500 nM, and we found good correlations (R2 = 0.89, S. aureus; R2 = 0.79, E. coli) between experimental and predicted cell growth inhibition by using DNA DeltaTm and UPPS IC50 experimental results together with one computed descriptor. We also solved the structures of three bisamidines binding to DNA as well as three UPPS structures. Overall, the results are of general interest in the context of the development of resistance-resistant antibiotics that involve multitargeting.
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The entry 3wyi is ON HOLD until Paper Publication
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Antibacterial Drug Leads: DNA and Enzyme Multitargeting.,Zhu W, Wang Y, Li K, Gao J, Huang CH, Chen CC, Ko TP, Zhang Y, Guo RT, Oldfield E J Med Chem. 2015 Jan 22. PMID:25574764<ref>PMID:25574764</ref>
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Authors: Gao, J., Ko, T.P., Huang, C.H., Oldfield, E., Guo, R.T.
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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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Description: Structure of S. aureus undecaprenyl diphosphate synthase
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== References ==
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[[Category: Unreleased Structures]]
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Gao, J]]
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[[Category: Guo, R T]]
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[[Category: Huang, C H]]
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[[Category: Ko, T P]]
[[Category: Oldfield, E]]
[[Category: Oldfield, E]]
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[[Category: Ko, T.P]]
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[[Category: Isopentenyl diphosphate binding]]
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[[Category: Huang, C.H]]
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[[Category: Product inhibition]]
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[[Category: Guo, R.T]]
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[[Category: Transferase]]
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[[Category: Gao, J]]
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Revision as of 15:45, 7 February 2015

Structure of S. aureus undecaprenyl diphosphate synthase

3wyi, resolution 2.00Å

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