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On the Regio‐ and Stereospecificity of Arachidonic Acid Peroxidation Catalyzed by Mammalian 15‐Lypoxygenases: A Combined Molecular Dynamics and QM/MM Study

dc.contributor.authorSuardíaz Delrío, Reynier
dc.contributor.authorMasgrau, Laura
dc.contributor.authorLluch, José
dc.contributor.authorGonzález‐Lafont, Àngels
dc.date.accessioned2024-01-11T11:24:04Z
dc.date.available2024-01-11T11:24:04Z
dc.date.issued2013
dc.description.abstract15-Lipoxygenases (15-LOs) catalyse the peroxidation reaction of arachidonic acid (AA) in mammals with remarkable regioand stereospecificity. This positional-specific peroxidation is of paramount importance because it determines the nature and biological functions of the final metabolites generated by each LO as a result of the oxidative metabolism of AA. Although several hypotheses have been formulated concerning the regio- and stereospecificity of LOs, the molecular basis of such behaviour is still unclear. Herein, we combined quantum mechanics/molecular mechanics calculations with molecular dynamics simulations of the complete rabbit 15-LO/AA solvated model to examine the most accepted hypotheses for the regio- and stereospecificity of LOs. We have found that the clue to explain this specificity is the oxygen-targeting hypothesis through steric shielding of specific residues (mainly Leu597, Gln548 and Phe175, as well as the AA tail itself). Our deductions are based primarily on the analysis of the energy barrier heights from the oxygen addition reaction profiles
dc.description.departmentDepto. de Química Física
dc.description.facultyFac. de Ciencias Químicas
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Economía y Competitividad (España)
dc.description.sponsorshipGeneralitat de Catalunya
dc.description.sponsorshipAlianza 4U
dc.description.statuspub
dc.identifier.citationSuardíaz, Reynier, et al. «On the Regio‐ and Stereospecificity of Arachidonic Acid Peroxidation Catalyzed by Mammalian 15‐Lypoxygenases: A Combined Molecular Dynamics and QM/MM Study». ChemPhysChem, vol. 14, n.o 16, noviembre de 2013, pp. 3777-87. https://doi.org/10.1002/cphc.201300629.
dc.identifier.doi10.1002/cphc.201300629
dc.identifier.essn1439-7641
dc.identifier.issn1439-4235
dc.identifier.officialurlhttps://doi.org/10.1002/cphc.201300629
dc.identifier.urihttps://hdl.handle.net/20.500.14352/92499
dc.issue.number16
dc.journal.titleChemPhysChem
dc.language.isoeng
dc.page.final3787
dc.page.initial3777
dc.publisherWiley
dc.relation.projectIDinfo:eu-repo/grantAgreement/MICINN//CTQ2011-24292/ES/EXTENDIENDO LA QUIMICA TEORICA AL ESTUDIO DE LA CATALISIS ENZIMATICA Y DE LAS PROTEINAS FLUORESCENTES/
dc.relation.projectID2009SGR409
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.cdu544
dc.subject.keywordDensity functional calculations
dc.subject.keywordEnzymes
dc.subject.keywordPeroxidation
dc.subject.keywordRegioselectivity
dc.subject.keywordStereospecificity
dc.subject.ucmCiencias
dc.subject.unesco23 Química
dc.titleOn the Regio‐ and Stereospecificity of Arachidonic Acid Peroxidation Catalyzed by Mammalian 15‐Lypoxygenases: A Combined Molecular Dynamics and QM/MM Study
dc.typejournal article
dc.type.hasVersionAM
dc.volume.number14
dspace.entity.typePublication
relation.isAuthorOfPublication8b0c8e63-584d-4205-a5aa-81107b9bd474
relation.isAuthorOfPublication.latestForDiscovery8b0c8e63-584d-4205-a5aa-81107b9bd474

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