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dc.contributor.authorBridwell-Rabb, Jennifer
dc.contributor.authorDrennan, Catherine L
dc.date.accessioned2020-07-23T21:23:11Z
dc.date.available2020-07-23T21:23:11Z
dc.date.issued2017-02
dc.identifier.issn1879-0402
dc.identifier.urihttps://hdl.handle.net/1721.1/126368
dc.descriptionApril 2017 issue of Current Opinion in Chemical Biology is a special issue: "Biocatalysis & biotransformation * Bioinorganic Chemistry"en_US
dc.description.abstractThe ability of cobalamin to coordinate different upper axial ligands gives rise to a diversity of reactivity. Traditionally, adenosylcobalamin is associated with radical-based rearrangements, and methylcobalamin with methyl cation transfers. Recently, however, a new role for adenosylcobalamin has been discovered as a light sensor, and a methylcobalamin-dependent enzyme has been identified that is suggested to transfer a methyl anion. Additionally, recent studies have provided a wealth of new information about a third class of cobalamin-dependent enzymes that do not appear to use an upper ligand. They function in reductive dehalogenations and epoxide reduction reactions. Finally, mechanistic details are beginning to emerge about the cobalamin-dependent S-adenosylmethionine radical enzyme superfamily for which the role of cobalamin has been largely enigmatic. ©2017 Elsevier Ltden_US
dc.description.sponsorshipNational Institute of Health (Grant no. R01-GM69857)en_US
dc.description.sponsorshipNational Institute of Health Grant (F32-GM108189)en_US
dc.language.isoen
dc.publisherElsevier BVen_US
dc.relation.isversionofhttps://dx.doi.org/10.1016/J.CBPA.2017.01.013en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titleVitamin B 12 in the spotlight againen_US
dc.title.alternativeVitamin B[subscript 12] in the spotlight againen_US
dc.typeArticleen_US
dc.identifier.citationBridwell-Rabb, Jennifer and Catherine L. Drennan, "Vitamin B12 in the spotlight again." Current Opinion in Chemical Biology 37 (April 2017): p. 63-70 doi. 10.1016/j.cbpa.2017.01.013 ©2017 Authorsen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.relation.journalCurrent Opinion in Chemical Biologyen_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
dc.date.updated2019-09-18T12:45:02Z
dspace.date.submission2019-09-18T12:45:03Z
mit.journal.volume37en_US
mit.metadata.statusComplete


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