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dc.contributor.authorRoy, S
dc.contributor.authorVivoli Vega, M
dc.contributor.authorHarmer, NJ
dc.date.accessioned2019-01-09T16:08:11Z
dc.date.issued2019-01-02
dc.description.abstractCarbohydrate kinases activate a wide variety of monosaccharides by adding a phosphate group, usually from ATP. This modification is fundamental to saccharide utilization, and it is likely a very ancient reaction. Modern organisms contain carbohydrate kinases from at least five main protein families. These range from the highly specialized inositol kinases, to the ribokinases and galactokinases, which belong to families that phosphorylate a wide range of substrates. The carbohydrate kinases utilize a common strategy to drive the reaction between the sugar hydroxyl and the donor phosphate. Each sugar is held in position by a network of hydrogen bonds to the non-reactive hydroxyls (and other functional groups). The reactive hydroxyl is deprotonated, usually by an aspartic acid side chain acting as a catalytic base. The deprotonated hydroxyl then attacks the donor phosphate. The resulting pentacoordinate transition state is stabilized by an adjacent divalent cation, and sometimes by a positively charged protein side chain or the presence of an anion hole. Many carbohydrate kinases are allosterically regulated using a wide variety of strategies, due to their roles at critical control points in carbohydrate metabolism. The evolution of a similar mechanism in several folds highlights the elegance and simplicity of the catalytic scheme.en_GB
dc.description.sponsorshipBiotechnology & Biological Sciences Research Council (BBSRC)en_GB
dc.identifier.citationVol. 9 (1), article 29en_GB
dc.identifier.doi10.3390/catal9010029
dc.identifier.grantnumberBB/H019685/1en_GB
dc.identifier.urihttp://hdl.handle.net/10871/35411
dc.language.isoenen_GB
dc.publisherMDPIen_GB
dc.rights© 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).en_GB
dc.subjectphosphorylationen_GB
dc.subjecthexokinasesen_GB
dc.subjectROK kinasesen_GB
dc.subjectGHMP kinasesen_GB
dc.subjectphosphatidylinositol phosphate kinasesen_GB
dc.titleCarbohydrate Kinases: A Conserved Mechanism Across Differing Foldsen_GB
dc.typeArticleen_GB
dc.date.available2019-01-09T16:08:11Z
dc.identifier.issn2073-4344
dc.descriptionThis is the final version. Available from MDPI via the DOI in this recorden_GB
dc.identifier.journalCatalystsen_GB
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2018-12-21
exeter.funder::Biotechnology & Biological Sciences Research Council (BBSRC)en_GB
exeter.funder::Biotechnology & Biological Sciences Research Council (BBSRC)en_GB
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2019-01-02
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2019-01-09T13:38:21Z
refterms.versionFCDVoR
refterms.dateFOA2019-01-09T16:08:18Z
refterms.panelAen_GB


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© 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's licence is described as © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).