5hn9

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'''Unreleased structure'''
 
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The entry 5hn9 is ON HOLD until Paper Publication
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==Crystal structure of Plasmodium vivax geranylgeranylpyrophosphate synthase complexed with BPH-1186==
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<StructureSection load='5hn9' size='340' side='right' caption='[[5hn9]], [[Resolution|resolution]] 2.12&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5hn9]] is a 4 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5HN9 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5HN9 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=04W:2-{[3-(DECYLOXY)BENZYL]OXY}-5-NITROBENZOIC+ACID'>04W</scene></td></tr>
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<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5hn7|5hn7]], [[5hn8|5hn8]], [[5hna|5hna]]</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=5hn9 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5hn9 OCA], [http://pdbe.org/5hn9 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5hn9 RCSB], [http://www.ebi.ac.uk/pdbsum/5hn9 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5hn9 ProSAT]</span></td></tr>
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</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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We report a molecular dynamics investigation of the structure, function, and inhibition of geranylgeranyl diphosphate synthase (GGPPS), a potential drug target, from the malaria parasite Plasmodium vivax. We discovered several GGPPS inhibitors, benzoic acids, and determined their structures crystallographically. We then used molecular dynamics simulations to investigate the dynamics of three such inhibitors and two bisphosphonate inhibitors, zoledronate and a lipophilic analogue of zoledronate, as well as the enzyme's product, GGPP. We were able to identify the main motions that govern substrate binding and product release as well as the molecular features required for GGPPS inhibition by both classes of inhibitor. The results are of broad general interest because they represent the first detailed investigation of the mechanism of action, and inhibition, of an important antimalarial drug target, geranylgeranyl diphosphate synthase, and may help guide the development of other, novel inhibitors as new drug leads.
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Authors: Liu, Y.-L., Zhang, Y., OIdfield, E.
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Dynamic Structure and Inhibition of a Malaria Drug Target: Geranylgeranyl Diphosphate Synthase.,G Ricci C, Liu YL, Zhang Y, Wang Y, Zhu W, Oldfield E, McCammon JA Biochemistry. 2016 Sep 1. PMID:27564465<ref>PMID:27564465</ref>
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Description: Crystal structure of Plasmodium vivax geranylgeranylpyrophosphate synthase complexed with BPH-1186
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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 5hn9" 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: Liu, Y L]]
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[[Category: OIdfield, E]]
[[Category: Zhang, Y]]
[[Category: Zhang, Y]]
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[[Category: Oidfield, E]]
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[[Category: All helice]]
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[[Category: Liu, Y.-L]]
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[[Category: Transferase]]
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[[Category: Transferase-transferase inhibitor complex]]

Revision as of 06:15, 21 September 2016

Crystal structure of Plasmodium vivax geranylgeranylpyrophosphate synthase complexed with BPH-1186

5hn9, resolution 2.12Å

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