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dc.contributor.authorArand, Michaelde
dc.contributor.authorCronin, Annettede
dc.contributor.authorHengstler, Jan G.de
dc.contributor.authorHerrero Plana, Maria Elenade
dc.contributor.authorLohmann, Matthiasde
dc.contributor.authorOesch, Franzde
dc.date.accessioned2008-06-17T13:35:50Z-
dc.date.available2008-06-17T13:35:50Z-
dc.date.issued2003-03-13de
dc.identifier.issn1611-2156de
dc.identifier.urihttp://hdl.handle.net/2003/25628-
dc.identifier.urihttp://dx.doi.org/10.17877/DE290R-117-
dc.description.abstractThe human microsomal epoxide hydrolase, a single enzyme, has to detoxify a broad range of structurally diverse, potentially genotoxic epoxides that are formed in the course of xenobiotic metabolism. The enzyme has developed a unique strategy to combine a broad substrate specificity with a high detoxification efficacy, by immediately trapping the reactive compounds as covalent intermediates and by being expressed at high levels for high trapping capacity. Computer simulation and experimental data as well as existing epidemiologic studies reveal this detoxification strategy as the mechanistic basis for a threshold in the tumorigenesis of mutagenic carcinogens.en
dc.language.isoende
dc.relation.ispartofseriesEXCLI Journal ; Vol. 2, 2003en
dc.subjectcomputer simulationen
dc.subjectenzyme kineticsen
dc.subjectgenotoxicen
dc.subjectmechanismen
dc.subjectstructureen
dc.subject.ddc610de
dc.titleDetoxification Strategy of Epoxide Hydrolaseen
dc.title.alternativeThe Basis for a Threshold in Chemical Carcinogenesisen
dc.typeTextde
dc.type.publicationtypearticlede
dcterms.accessRightsopen access-
eldorado.dnb.zdberstkatid2132560-1-
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