Computational Study of the Phosphoryl Donor Activity of Dihydroxyacetone Kinase from ATP to Inorganic Polyphosphate
Impacto
Scholar |
Otros documentos de la autoría: Bordes, Isabel; García-Junceda, Eduardo; Sánchez Moreno, Israel; Castillo, Raquel; Moliner, Vicent
Metadatos
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INVESTIGACIONMetadatos
Título
Computational Study of the Phosphoryl Donor Activity of Dihydroxyacetone Kinase from ATP to Inorganic PolyphosphateAutoría
Fecha de publicación
2017-10Editor
WileyCita bibliográfica
BORDES, Isabel, et al. Computational study of the phosphoryl donor activity of dihydroxyacetone kinase from ATP to inorganic polyphosphate. International Journal of Quantum Chemistry, 2017.Tipo de documento
info:eu-repo/semantics/articleVersión de la editorial
http://onlinelibrary.wiley.com/doi/10.1002/qua.25520/fullVersión
info:eu-repo/semantics/submittedVersionPalabras clave / Materias
Resumen
Adenosine triphosphate (ATP) is the main biological phosphoryl donor required in many enzymes including dihydroxyacetone kinases (DHAKs) that convert dihydroxyacetone (Dha) into dihydroxyacetone phosphate (Dha-P), a ... [+]
Adenosine triphosphate (ATP) is the main biological phosphoryl donor required in many enzymes including dihydroxyacetone kinases (DHAKs) that convert dihydroxyacetone (Dha) into dihydroxyacetone phosphate (Dha-P), a key species with potential applications in synthesis. Herein, we present a theoretical study of the molecular mechanism for the phosphoryl transfer reaction from an inorganic polyphosphate to Dha catalyzed by DHAK from C. freundii. This is part of a project devoted to modify the phosphoryl donor specificity of this enzyme avoiding the use of the problematic direct addition of ATP. Based on the use of hybrid QM/MM potentials, with the QM region described by semiempirical and DFT methods, the reaction mechanism of the wild-type enzyme and the most active experimentally measured mutant (Glu526Lys) with poly-P as phosphoryl donor has been explored to elucidate the origin of the activity of this mutant. The similar energy barriers obtained in both systems confirm our previous studies on the binding step (Sánchez-Moreno et al., Int. J. Mol. Sci. 2015, 16, 27835) suggesting that this mutation favors a more adequate position of the poly-P in the active site for the following step, the chemical reaction, to take place. [-]
Proyecto de investigación
Spanish Ministerio de Economía y Competitividad for project CTQ2015-66223-C2; Universitat Jaume I (project P1•1B2014-26); Generalitat Valenciana (PROMETEOII/2014/022); Universitat Jaume I (project P1•1B2014-26 and P1•1B2013-58); University of Bath (David Parkin Visiting Professorship)Derechos de acceso
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