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dc.contributor.authorAbdussalam Adina-Zadaen_US
dc.contributor.authorChutima Sereeruken_US
dc.contributor.authorSarawut Jitrapakdeeen_US
dc.contributor.authorTonya N. Zeczyckien_US
dc.contributor.authorMartin St. Mauriceen_US
dc.contributor.authorW. Wallace Clelanden_US
dc.contributor.authorJohn C. Wallaceen_US
dc.contributor.authorPaul V. Attwooden_US
dc.contributor.otherUniversity of Western Australiaen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherThe Brody School of Medicineen_US
dc.contributor.otherMarquette Universityen_US
dc.contributor.otherUniversity of Wisconsin Madison, Institute for Enzyme Researchen_US
dc.contributor.otherUniversity of Adelaideen_US
dc.date.accessioned2018-06-11T04:33:17Z-
dc.date.available2018-06-11T04:33:17Z-
dc.date.issued2012-10-16en_US
dc.identifier.citationBiochemistry. Vol.51, No.41 (2012), 8208-8217en_US
dc.identifier.issn15204995en_US
dc.identifier.issn00062960en_US
dc.identifier.other2-s2.0-84867552931en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84867552931&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/13592-
dc.description.abstractMutation of Arg427 and Arg472 in Rhizobium etli pyruvate carboxylase to serine or lysine greatly increased the activation constant (K a ) of acetyl CoA, with the increase being greater for the Arg472 mutants. These results indicate that while both these residues are involved in the binding of acetyl CoA to the enzyme, Arg472 is more important than Arg427. The mutations had substantially smaller effects on the k cat for pyruvate carboxylation. Part of the effects of the mutations was to increase the K m for MgATP and the K a for activation by free Mg 2+ determined at saturating acetyl CoA concentrations. The inhibitory effects of the mutations on the rates of the enzyme-catalyzed bicarbonate-dependent ATP cleavage, carboxylation of biotin, and phosphorylation of ADP by carbamoyl phosphate indicate that the major locus of the effects of the mutations was in the biotin carboxylase (BC) domain active site. Even though both Arg427 and Arg472 are distant from the BC domain active site, it is proposed that their contacts with other residues in the allosteric domain, either directly or through acetyl CoA, affect the positioning and orientation of the biotin-carboxyl carrier protein (BCCP) domain and thus the binding of biotin at the BC domain active site. On the basis of the kinetic analysis proposed here, it is proposed that mutations of Arg427 and Arg472 perturb these contacts and consequently the binding of biotin at the BC domain active site. Inhibition of pyruvate carboxylation by the allosteric inhibitor l-aspartate was largely unaffected by the mutation of either Arg427 or Arg472. © 2012 American Chemical Society.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84867552931&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleRoles of Arg427 and Arg472 in the binding and allosteric effects of acetyl CoA in pyruvate carboxylaseen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1021/bi301060den_US
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