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dc.contributor.authorBehan, Rachel K.
dc.contributor.authorLippard, Stephen J.
dc.date.accessioned2011-12-19T18:07:45Z
dc.date.available2011-12-19T18:07:45Z
dc.date.issued2010-10
dc.date.submitted2010-09
dc.identifier.issn0006-2960
dc.identifier.issn1520-4995
dc.identifier.urihttp://hdl.handle.net/1721.1/67722
dc.description.abstractThe aging-associated enzyme CLK-1 is proposed to be a member of the carboxylate-bridged diiron family of proteins. To evaluate this hypothesis and characterize the protein, we expressed soluble mouse CLK-1 (MCLK1) in Escherichia coli as a heterologous host. Using Mossbauer and EPR spectroscopy, we established that MCLK1 indeed belongs to this protein family. Biochemical analyses of the in vitro activity of MCLK1 with quinone substrates revealed that NADH can serve directly as a reductant for catalytic activation of dioxygen and substrate oxidation by the enzyme, with no requirement for an additional reductase protein component. The direct reaction of NADH with a diiron-containing oxidase enzyme has not previously been encountered for any member of the protein superfamily.en_US
dc.description.sponsorshipNational Institute of General Medical Sciences (U.S.) (grant GM032134)en_US
dc.description.sponsorshipNational Institute of General Medical Sciences (U.S.) (NIGMS (1 F32 GM084564-03))en_US
dc.language.isoen_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/bi101475zen_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceProf. Lippard via Erja Kajosaloen_US
dc.titleThe Aging-Associated Enzyme CLK-1 is a Member of the Carboxylate-Bridged Diiron Family of Proteinsen_US
dc.typeArticleen_US
dc.identifier.citationBehan, Rachel K., and Stephen J. Lippard. “The Aging-Associated Enzyme CLK-1 Is a Member of the Carboxylate-Bridged Diiron Family of Proteins.” Biochemistry 49.45 (2010): 9679-9681.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.approverLippard, Stephen J.
dc.contributor.mitauthorBehan, Rachel K.
dc.contributor.mitauthorLippard, Stephen J.
dc.relation.journalBiochemistryen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsBehan, Rachel K.; Lippard, Stephen J.en
dc.identifier.orcidhttps://orcid.org/0000-0002-2693-4982
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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