Literature DB >> 21513457

Biological phosphoryl-transfer reactions: understanding mechanism and catalysis.

Jonathan K Lassila1, Jesse G Zalatan, Daniel Herschlag.   

Abstract

Phosphoryl-transfer reactions are central to biology. These reactions also have some of the slowest nonenzymatic rates and thus require enormous rate accelerations from biological catalysts. Despite the central importance of phosphoryl transfer and the fascinating catalytic challenges it presents, substantial confusion persists about the properties of these reactions. This confusion exists despite decades of research on the chemical mechanisms underlying these reactions. Here we review phosphoryl-transfer reactions with the goal of providing the reader with the conceptual and experimental background to understand this body of work, to evaluate new results and proposals, and to apply this understanding to enzymes. We describe likely resolutions to some controversies, while emphasizing the limits of our current approaches and understanding. We apply this understanding to enzyme-catalyzed phosphoryl transfer and provide illustrative examples of how this mechanistic background can guide and deepen our understanding of enzymes and their mechanisms of action. Finally, we present important future challenges for this field.

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Year:  2011        PMID: 21513457      PMCID: PMC3418923          DOI: 10.1146/annurev-biochem-060409-092741

Source DB:  PubMed          Journal:  Annu Rev Biochem        ISSN: 0066-4154            Impact factor:   23.643


  97 in total

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  129 in total

1.  Crystal structure of release factor RF3 trapped in the GTP state on a rotated conformation of the ribosome.

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Journal:  RNA       Date:  2011-12-20       Impact factor: 4.942

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4.  The Positively Charged Active Site of the Bacterial Toxin RelE Causes a Large Shift in the General Base pKa.

Authors:  David A Hiller; Brian F Dunican; Sunitha Nallur; Nan-Sheng Li; Joseph A Piccirilli; Scott A Strobel
Journal:  Biochemistry       Date:  2020-04-24       Impact factor: 3.162

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6.  Arginine as a general acid catalyst in serine recombinase-mediated DNA cleavage.

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7.  Analysis of the RNA Binding Specificity Landscape of C5 Protein Reveals Structure and Sequence Preferences that Direct RNase P Specificity.

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8.  Analysis of Density Functional Tight Binding with Natural Bonding Orbitals.

Authors:  Xiya Lu; Juan Duchimaza-Heredia; Qiang Cui
Journal:  J Phys Chem A       Date:  2019-08-15       Impact factor: 2.781

9.  Nonconserved active site residues modulate CheY autophosphorylation kinetics and phosphodonor preference.

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10.  QM/MM free energy simulations: recent progress and challenges.

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