dc.creatorWang, Jingling
dc.creatorNiemevz, Fernando
dc.creatorLad, Latesh
dc.creatorHuang, Liusheng
dc.creatorAlvarez, Diego Ezequiel
dc.creatorBuldain, Graciela Yolanda
dc.creatorPoulos, Thomas L.
dc.creatorOrtiz de Montellano, Paul R.
dc.date.accessioned2018-05-04T18:51:36Z
dc.date.accessioned2018-11-06T12:57:50Z
dc.date.available2018-05-04T18:51:36Z
dc.date.available2018-11-06T12:57:50Z
dc.date.created2018-05-04T18:51:36Z
dc.date.issued2004-10
dc.identifierWang, Jingling; Niemevz, Fernando; Lad, Latesh; Huang, Liusheng; Alvarez, Diego Ezequiel; et al.; Human Heme Oxygenase Oxidation of 5- and 15-Phenylhemes; American Society for Biochemistry and Molecular Biology; Journal of Biological Chemistry (online); 279; 41; 10-2004; 42593-42604
dc.identifier0021-9258
dc.identifierhttp://hdl.handle.net/11336/44201
dc.identifier1083-351X
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1871674
dc.description.abstractHuman heme oxygenase-1 (hHO-1) catalyzes the O2- dependent oxidation of heme to biliverdin, CO, and free iron. Previous work indicated that electrophilic addition of the terminal oxygen of the ferric hydroperoxo complex to the -meso-carbon gives 5-hydroxyheme. Earlier efforts to block this reaction with a 5-methyl substituent failed, as the reaction still gave biliverdin IX . Surprisingly, a 15-methyl substituent caused exclusive cleavage at the -meso- rather than at the normal, unsubstituted -meso-carbon. No CO was formed in these reactions, but the fragment cleaved from the porphyrin eluded identification. We report here that hHO-1 cleaves 5-phenylheme to biliverdin IX and oxidizes 15- phenylheme at the -meso position to give 10-phenylbiliverdin IX . The fragment extruded in the oxidation of 5-phenylheme is benzoic acid, one oxygen of which comes from O2 and the other from water. The 2.29- and 2.11-Å crystal structures of the hHO-1 complexes with 1- and 15-phenylheme, respectively, show clear electron density for both the 5- and 15-phenyl rings in both molecules of the asymmetric unit. The overall structure of 15-phenylheme-hHO-1 is similar to that of heme-hHO-1 except for small changes in distal residues 141–150 and in the proximal Lys18 and Lys22. In the 5-phenylhemehHO-1 structure, the phenyl-substituted heme occupies the same position as heme in the heme-HO-1 complex but the 5-phenyl substituent disrupts the rigid hydrophobic wall of residues Met34, Phe214, and residues 26–42 near the -meso carbon. The results provide independent support for an electrophilic oxidation mechanism and support a role for stereochemical control of the reaction regiospecificity.
dc.languageeng
dc.publisherAmerican Society for Biochemistry and Molecular Biology
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://www.jbc.org/content/279/41/42593
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1074/jbc.M406346200
dc.rightshttps://creativecommons.org/licenses/by/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectHeme oxygenase
dc.subjectOxidizes heme to biliverdin
dc.subjectThe rate-limiting enzyme in the heme degradation pathway
dc.subjectCarbon monoxide
dc.subjectFree iron
dc.titleHuman Heme Oxygenase Oxidation of 5- and 15-Phenylhemes
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


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