<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-28T20:41:06Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/92519" metadataPrefix="qdc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/92519</identifier><datestamp>2024-08-01T00:07:18Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>Introducing Mutations to Modify the C13/C9 Ratio in Linoleic Acid Oxygenations Catalyzed by Rabbit 15‐Lipoxygenase: A QM/MM and MD Study</dc:title>
   <dc:creator>Suardíaz Delrío, Reynier</dc:creator>
   <dc:creator>Masgrau, Laura</dc:creator>
   <dc:creator>Lluch, José </dc:creator>
   <dc:creator>González‐Lafont, Àngels</dc:creator>
   <dcterms:abstract>Lipoxygenases (LOs) are a family of nonheme iron-containing enzymes that catalyze the hydroperoxidation of several polyunsaturated fatty acids with a huge regio- and stereospecificity. Mammalian 15-LO-1 yields almost exclusively oxygenation at the C13 position of the linoleic acid (LA), its preferred substrate. This is very important because metabolites derived from oxidation in distinct positions produce opposite physiological effects. We have combined here quantum mechanics/molecular mechanics calculations with molecular dynamics simulations to show how a suitable mutation of the rabbit 15-LO1 enzyme can produce a significant amount of products derived from oxygenation at the C9 position of LA. In effect, the Leu597Val or Leu597Ala mutants are predicted to lead to a diminution of the oxygenation C13/C9 ratio in LA as huge as five orders of magnitude. This shows that the conserved residue Leu597 actually drives the regiospecific hydroperoxidation of LA catalyzed by 15-LO-1 enzyme</dcterms:abstract>
   <dcterms:dateAccepted>2024-01-11T12:01:00Z</dcterms:dateAccepted>
   <dcterms:available>2024-01-11T12:01:00Z</dcterms:available>
   <dcterms:created>2024-01-11T12:01:00Z</dcterms:created>
   <dcterms:issued>2014</dcterms:issued>
   <dc:type>journal article</dc:type>
   <dc:identifier>https://hdl.handle.net/20.500.14352/92519</dc:identifier>
   <dc:identifier>1439-4235</dc:identifier>
   <dc:identifier>10.1002/cphc.201402471</dc:identifier>
   <dc:identifier>1439-7641</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>info:eu-repo/grantAgreement/MICINN//CTQ2011-24292/ES/EXTENDIENDO LA QUIMICA TEORICA AL ESTUDIO DE LA CATALISIS ENZIMATICA Y DE LAS PROTEINAS FLUORESCENTES/</dc:relation>
   <dc:relation>2009SGR409</dc:relation>
   <dc:relation>Suardíaz, R., Masgrau, L., Lluch, J.M. and González-Lafont, À. (2014), Introducing Mutations to Modify the C13/C9 Ratio in Linoleic Acid Oxygenations Catalyzed by Rabbit 15-Lipoxygenase: A QM/MM and MD Study. ChemPhysChem, 15: 4049-4054. https://doi.org/10.1002/cphc.201402471</dc:relation>
   <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
   <dc:rights>restricted access</dc:rights>
   <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
   <dc:publisher>Wiley</dc:publisher>
</qdc:qualifieddc></metadata></record></GetRecord></OAI-PMH>