5l51
From Proteopedia
(Difference between revisions)
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- | '''Unreleased structure''' | ||
- | + | ==Menthone neomenthol reductase from Mentha piperita== | |
+ | <StructureSection load='5l51' size='340' side='right' caption='[[5l51]], [[Resolution|resolution]] 2.66Å' scene=''> | ||
+ | == Structural highlights == | ||
+ | <table><tr><td colspan='2'>[[5l51]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5L51 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5L51 FirstGlance]. <br> | ||
+ | </td></tr><tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/(+)-neomenthol_dehydrogenase (+)-neomenthol dehydrogenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.1.1.208 1.1.1.208] </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=5l51 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5l51 OCA], [http://pdbe.org/5l51 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5l51 RCSB], [http://www.ebi.ac.uk/pdbsum/5l51 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5l51 ProSAT]</span></td></tr> | ||
+ | </table> | ||
+ | <div style="background-color:#fffaf0;"> | ||
+ | == Publication Abstract from PubMed == | ||
+ | Three enzymes of the Mentha essential oil biosynthetic pathway are highly homologous, namely the ketoreductases (-)-menthone:(-)-menthol reductase and (-)-menthone:(+)-neomenthol reductase, and the "ene" reductase isopiperitenone reductase. We identified a rare catalytic residue substitution in the last two, and performed comparative crystal structure analyses and residue-swapping mutagenesis to investigate whether this determines the reaction outcome. The result was a complete loss of native activity and a switch between ene reduction and ketoreduction. This suggests the importance of a catalytic glutamate vs. tyrosine residue in determining the outcome of the reduction of alpha,beta-unsaturated alkenes, due to the substrate occupying different binding conformations, and possibly also to the relative acidities of the two residues. This simple switch in mechanism by a single amino acid substitution could potentially generate a large number of de novo ene reductases. | ||
- | + | Pinpointing a Mechanistic Switch Between Ketoreduction and "Ene" Reduction in Short-Chain Dehydrogenases/Reductases.,Lygidakis A, Karuppiah V, Hoeven R, Ni Cheallaigh A, Leys D, Gardiner JM, Toogood HS, Scrutton NS Angew Chem Int Ed Engl. 2016 Aug 8;55(33):9596-600. doi: 10.1002/anie.201603785. , Epub 2016 Jul 13. PMID:27411040<ref>PMID:27411040</ref> | |
- | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |
- | [[Category: | + | </div> |
+ | <div class="pdbe-citations 5l51" style="background-color:#fffaf0;"></div> | ||
+ | == References == | ||
+ | <references/> | ||
+ | __TOC__ | ||
+ | </StructureSection> | ||
+ | [[Category: Karuppiah, V]] | ||
+ | [[Category: Leys, D]] | ||
+ | [[Category: Scrutton, N S]] | ||
+ | [[Category: Toogood, H S]] | ||
+ | [[Category: Isomenthone]] | ||
+ | [[Category: Menthone]] | ||
+ | [[Category: Oxidoreductase]] | ||
+ | [[Category: Rossmann fold]] |
Revision as of 14:00, 10 September 2016
Menthone neomenthol reductase from Mentha piperita
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