6onm
From Proteopedia
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| - | '''Unreleased structure''' | ||
| - | + | ==Crystal Structure of (+)-Limonene Synthase Complexed with 8,9-Difluorolinalyl Diphosphate== | |
| + | <StructureSection load='6onm' size='340' side='right'caption='[[6onm]], [[Resolution|resolution]] 2.70Å' scene=''> | ||
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>[[6onm]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Citsi Citsi]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6ONM OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6ONM FirstGlance]. <br> | ||
| + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=MN:MANGANESE+(II)+ION'>MN</scene>, <scene name='pdbligand=MWG:(3R)-8-fluoro-7-(fluoromethyl)-3-methylocta-1,6-dien-3-yl+trihydrogen+diphosphate'>MWG</scene></td></tr> | ||
| + | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/(R)-limonene_synthase (R)-limonene synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=4.2.3.20 4.2.3.20] </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=6onm FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6onm OCA], [http://pdbe.org/6onm PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6onm RCSB], [http://www.ebi.ac.uk/pdbsum/6onm PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6onm ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | <div style="background-color:#fffaf0;"> | ||
| + | == Publication Abstract from PubMed == | ||
| + | Linalyl diphosphate (LPP) is the postulated intermediate in the enzymatic cyclization of monoterpenes catalyzed by terpene synthases. LPP is considered an obligate intermediate due to the conformationally restrictive trans-C2-C3 double bond of the substrate, geranyl diphosphate (GPP), which precludes the proper positioning of carbons C1 and C6 to enable cyclization. However, because of the complexity of potential carbocation-mediated rearrangements in these enzymatic reactions, it has proven difficult to directly demonstrate the formation of LPP despite significant efforts. Here we synthesized a fluorinated substrate analog, 8,9-difluorogeranyl diphosphate (DFGPP), which is designed to allow initial ionization/isomerization and form the fluorinated equivalent of LPP (DFLPP) while preventing the subsequent ionization/cyclization to produce the alpha-terpinyl cation. Steady-state kinetic studies with the model enzyme (+)-limonene synthase (LS) under catalytic conditions show that the cyclization of DFGPP is completely blocked and a single linear product, difluoromyrcene, is produced. When crystals of apo-LS are soaked with DFGPP under conditions limiting turnover of the enzyme, we show, using X-ray crystallography, that DFLPP is produced in the enzyme active site and trapped in the crystals. Clear electron density is observed in the active site of the enzyme, but it cannot be appropriately fit with a model for the DFGPP substrate analog, whereas it can accommodate an extended conformation of DFLPP. This result supports the current model for monoterpene cyclization by providing direct evidence of LPP as an intermediate. | ||
| - | + | Direct Evidence of an Enzyme-Generated LPP Intermediate in (+)-Limonene Synthase Using a Fluorinated GPP Substrate Analog.,Morehouse BR, Kumar RP, Matos JO, Yu Q, Bannister A, Malik K, Temme JS, Krauss IJ, Oprian DD ACS Chem Biol. 2019 Sep 20;14(9):2035-2043. doi: 10.1021/acschembio.9b00514. Epub, 2019 Sep 4. PMID:31433159<ref>PMID:31433159</ref> | |
| - | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |
| - | [[Category: | + | </div> |
| + | <div class="pdbe-citations 6onm" style="background-color:#fffaf0;"></div> | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Citsi]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Kumar, R Prem]] | ||
| + | [[Category: Morehouse, B R]] | ||
| + | [[Category: Oprian, D D]] | ||
| + | [[Category: Yu, Q]] | ||
| + | [[Category: Enantiomer]] | ||
| + | [[Category: Fluoro analog]] | ||
| + | [[Category: Lyase]] | ||
| + | [[Category: Metal binding]] | ||
| + | [[Category: Monoterpene]] | ||
| + | [[Category: Terpene synthase]] | ||
| + | [[Category: Terpene synthase fold]] | ||
Revision as of 11:15, 2 October 2019
Crystal Structure of (+)-Limonene Synthase Complexed with 8,9-Difluorolinalyl Diphosphate
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