dc.contributor.author | Behan, Rachel K. | |
dc.contributor.author | Lippard, Stephen J. | |
dc.date.accessioned | 2011-12-19T18:07:45Z | |
dc.date.available | 2011-12-19T18:07:45Z | |
dc.date.issued | 2010-10 | |
dc.date.submitted | 2010-09 | |
dc.identifier.issn | 0006-2960 | |
dc.identifier.issn | 1520-4995 | |
dc.identifier.uri | http://hdl.handle.net/1721.1/67722 | |
dc.description.abstract | The 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.sponsorship | National Institute of General Medical Sciences (U.S.) (grant GM032134) | en_US |
dc.description.sponsorship | National Institute of General Medical Sciences (U.S.) (NIGMS (1 F32 GM084564-03)) | en_US |
dc.language.iso | en_US | |
dc.publisher | American Chemical Society | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1021/bi101475z | en_US |
dc.rights | Article 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.source | Prof. Lippard via Erja Kajosalo | en_US |
dc.title | The Aging-Associated Enzyme CLK-1 is a Member of the Carboxylate-Bridged Diiron Family of Proteins | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Behan, 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.department | Massachusetts Institute of Technology. Department of Chemistry | en_US |
dc.contributor.approver | Lippard, Stephen J. | |
dc.contributor.mitauthor | Behan, Rachel K. | |
dc.contributor.mitauthor | Lippard, Stephen J. | |
dc.relation.journal | Biochemistry | en_US |
dc.eprint.version | Author's final manuscript | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dspace.orderedauthors | Behan, Rachel K.; Lippard, Stephen J. | en |
dc.identifier.orcid | https://orcid.org/0000-0002-2693-4982 | |
mit.license | PUBLISHER_POLICY | en_US |
mit.metadata.status | Complete | |