Conserved phosphoryl transfer mechanisms within kinase families and the role of the C8 proton of ATP in the activation of phosphoryl transfer

BackgroundThe kinome is made up of a large number of functionally diverse enzymes, with the classification indicating very little about the extent of the conserved kinetic mechanisms associated with phosphoryl transfer. It has been demonstrated that C8-H of ATP plays a critical role in the activity of a range of kinase and synthetase enzymes.ResultsA number of conserved mechanisms within the prescribed kinase fold families have been identified directly utilizing the C8-H of ATP in the initiation of phosphoryl transfer. These mechanisms are based on structurally conserved amino acid residues that are within hydrogen bonding distance of a co-crystallized nucleotide. On the basis of these conserved mechanisms, the role of the nucleotide C8-H in initiating the formation of a pentavalent intermediate between the γ-phosphate of the ATP and the substrate nucleophile is defined. All reactions can be clustered into two mechanisms by which the C8-H is induced to be labile via the coordination of a backbone carbonyl to C6-NH2 of the adenyl moiety, namely a "push" mechanism, and a "pull" mechanism, based on the protonation of N7. Associated with the "push" mechanism and "pull" mechanisms are a series of proton transfer cascades, initiated from C8-H, via the tri-phosphate backbone, culminating in the formation of the pentavalent transition state between the γ-phosphate of the ATP and the substrate nucleophile.ConclusionsThe "push" mechanism and a "pull" mechanism are responsible for inducing the C8-H of adenyl moiety to become more labile. These mechanisms and the associated proton transfer cascades achieve the proton transfer via different family-specific conserved sets of amino acids. Each of these mechanisms would allow for the regulation of the rate of formation of the pentavalent intermediate between the ATP and the substrate nucleophile. Phosphoryl transfer within kinases is therefore a specific event mediated and regulated via the coordination of the adenyl moiety of ATP and the C8-H of the adenyl moiety.

[1]  S. Yokoyama,et al.  Structure of selenophosphate synthetase essential for selenium incorporation into proteins and RNAs. , 2009, Journal of molecular biology.

[2]  A. Dillmann Enzyme Nomenclature , 1965, Nature.

[3]  Nick V Grishin,et al.  Sequence and structure classification of kinases. , 2002, Journal of molecular biology.

[4]  S. Kim,et al.  High-resolution crystal structures of human cyclin-dependent kinase 2 with and without ATP: bound waters and natural ligand as guides for inhibitor design. , 1996, Journal of medicinal chemistry.

[5]  Nick V Grishin,et al.  A comprehensive update of the sequence and structure classification of kinases , 2015 .

[6]  P R Evans,et al.  Phosphofructokinase: structure and control. , 1981 .

[7]  D. Stammers,et al.  Structures of R- and T-state Escherichia coli Aspartokinase III , 2006, Journal of Biological Chemistry.

[8]  H. Matsuzawa,et al.  Structural basis for the ADP-specificity of a novel glucokinase from a hyperthermophilic archaeon. , 2001, Structure.

[9]  E V Koonin,et al.  AAA+: A class of chaperone-like ATPases associated with the assembly, operation, and disassembly of protein complexes. , 1999, Genome research.

[10]  Kornelia Polyak,et al.  Mechanism of CDK activation revealed by the structure of a cyclinA-CDK2 complex , 1995, Nature.

[11]  S. Heller 1-H NMR studies on deuterium-hydrogen exchange at C-5 in uridines. , 1968, Biochemical and biophysical research communications.

[12]  S. Taylor,et al.  Bound to activate: conformational consequences of cyclin binding to CDK2. , 1995, Structure.

[13]  D. M. Jacobsen,et al.  Briefly bound to activate: transient binding of a second catalytic magnesium activates the structure and dynamics of CDK2 kinase for catalysis. , 2011, Structure.

[14]  Wenqing Xu,et al.  Crystal structure of a polyphosphate kinase and its implications for polyphosphate synthesis , 2005, EMBO reports.

[15]  C. Kinsland,et al.  Structural studies of thiamin monophosphate kinase in complex with substrates and products. , 2008, Biochemistry.

[16]  A. Edison Linus Pauling and the planar peptide bond , 2001, Nature Structural Biology.

[17]  T. E. THORPE,et al.  The Composition of Water , 1888, Nature.

[18]  A. Fersht Structure and mechanism in protein science , 1998 .

[19]  S. De Carlo,et al.  Engagement of arginine finger to ATP triggers large conformational changes in NtrC1 AAA+ ATPase for remodeling bacterial RNA polymerase. , 2010, Structure.

[20]  Slawomir K. Grzechnik,et al.  Crystal structure of a glycerate kinase (TM1585) from Thermotoga maritima at 2.70 Å resolution reveals a new fold , 2006, Proteins.

[21]  A. R. Fresht Structure and Mechanism in Protein Science: A Guide to Enzyme Catalysis and Protein Folding , 1999 .

[22]  M. Hasson,et al.  Crystal Structure of Butyrate Kinase 2 from Thermotoga maritima, a Member of the ASKHA Superfamily of Phosphotransferases , 2009, Journal of bacteriology.

[23]  C. Rock,et al.  Analysis of the Staphylococcus aureus DgkB structure reveals a common catalytic mechanism for the soluble diacylglycerol kinases. , 2008, Structure.

[24]  B. Potter,et al.  Chemoenzymatic synthesis of 7-deaza cyclic adenosine 5'-diphosphate ribose analogues, membrane-permeant modulators of intracellular calcium release. , 2008, The Journal of organic chemistry.

[25]  Andrei L Osterman,et al.  Ligand binding-induced conformational changes in riboflavin kinase: structural basis for the ordered mechanism. , 2003, Biochemistry.

[26]  D. Bergstrom,et al.  Halogenation of tubercidin by N-halosuccinimides. A direct route to 5-bromotubercidin, a reversible inhibitor of RNA synthesis in eukaryotic cells. , 1980, Nucleic acids research.

[27]  Michael S. Deal,et al.  Activation mechanism of CDK2: role of cyclin binding versus phosphorylation. , 2002, Biochemistry.

[28]  W. Saenger,et al.  Structures of human N-Acetylglucosamine kinase in two complexes with N-Acetylglucosamine and with ADP/glucose: insights into substrate specificity and regulation. , 2006, Journal of molecular biology.

[29]  Martin Egli,et al.  Analysis of KaiA–KaiC protein interactions in the cyano‐bacterial circadian clock using hybrid structural methods , 2006, The EMBO journal.

[30]  H. Eklund,et al.  Functional studies of active‐site mutants from Drosophila melanogaster deoxyribonucleoside kinase , 2007, The FEBS journal.

[31]  M. S. Chapman,et al.  Transition state structure of arginine kinase: implications for catalysis of bimolecular reactions. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[32]  L. Delbaere,et al.  Mg2+–Mn2+ clusters in enzyme-catalyzed phosphoryl-transfer reactions , 1997, Nature Structural Biology.

[33]  W. Hunter,et al.  Structures of Staphylococcus aureus D-Tagatose-6-phosphate Kinase Implicate Domain Motions in Specificity and Mechanism* , 2007, Journal of Biological Chemistry.

[34]  P. Steenkamp,et al.  The role of the C8 proton of ATP in the regulation of phosphoryl transfer within kinases and synthetases , 2011, BMC Biochemistry.

[35]  H J Fromm,et al.  Crystal structures of mutant monomeric hexokinase I reveal multiple ADP binding sites and conformational changes relevant to allosteric regulation. , 2000, Journal of molecular biology.

[36]  Seok-Yong Lee,et al.  Regulation of the transcriptional activator NtrC1: structural studies of the regulatory and AAA+ ATPase domains. , 2003, Genes & development.

[37]  Sung-Hou Kim,et al.  Crystal structures of an NAD kinase from Archaeoglobus fulgidus in complex with ATP, NAD, or NADP. , 2005, Journal of molecular biology.

[38]  H. Eklund,et al.  Structure-function analysis of a bacterial deoxyadenosine kinase reveals the basis for substrate specificity. , 2007, Journal of molecular biology.

[39]  Robert Huber,et al.  Crystal structure of Schizosaccharomyces pombe riboflavin kinase reveals a novel ATP and riboflavin-binding fold. , 2003, Journal of molecular biology.

[40]  Tadhg P Begley,et al.  Crystal structure of 4-amino-5-hydroxymethyl-2-methylpyrimidine phosphate kinase from Salmonella typhimurium at 2.3 A resolution. , 2002, Structure.

[41]  E. Strauss,et al.  Structural basis for substrate binding and the catalytic mechanism of type III pantothenate kinase. , 2008, Biochemistry.

[42]  Lan-fen Li,et al.  Crystal structures of catalytic intermediates of human selenophosphate synthetase 1. , 2009, Journal of molecular biology.

[43]  Murray N. Robertson,et al.  Characterization of Aquifex aeolicus 4-diphosphocytidyl-2C-methyl-d-erythritol kinase – ligand recognition in a template for antimicrobial drug discovery , 2008, The FEBS journal.

[44]  C. Marco-Marín,et al.  The crystal structure of Pyrococcus furiosus UMP kinase provides insight into catalysis and regulation in microbial pyrimidine nucleotide biosynthesis. , 2005, Journal of molecular biology.

[45]  I. Schlichting,et al.  pH influences fluoride coordination number of the AlFx phosphoryl transfer transition state analog , 1999, Nature Structural Biology.

[46]  M. Walkinshaw,et al.  Allosteric Mechanism of Pyruvate Kinase from Leishmania mexicana Uses a Rock and Lock Model* , 2010, The Journal of Biological Chemistry.

[47]  A. Kornberg,et al.  Polyphosphate kinase from Escherichia coli. Purification and demonstration of a phosphoenzyme intermediate. , 1990, The Journal of biological chemistry.

[48]  D. Timm,et al.  Pyrithiamine as a Substrate for Thiamine Pyrophosphokinase* , 2006, Journal of Biological Chemistry.

[49]  S J Remington,et al.  Crystal structures of Escherichia coli glycerol kinase variant S58-->W in complex with nonhydrolyzable ATP analogues reveal a putative active conformation of the enzyme as a result of domain motion. , 1999, Biochemistry.

[50]  N. Grishin,et al.  Structure and mechanism of homoserine kinase: prototype for the GHMP kinase superfamily. , 2000, Structure.

[51]  Ignacio Fita,et al.  The course of phosphorus in the reaction of N-acetyl-L-glutamate kinase, determined from the structures of crystalline complexes, including a complex with an AlF(4)(-) transition state mimic. , 2003, Journal of molecular biology.

[52]  M. Walkinshaw,et al.  The crystal structure of ATP-bound phosphofructokinase from Trypanosoma brucei reveals conformational transitions different from those of other phosphofructokinases. , 2009, Journal of molecular biology.

[53]  F. Mackenzie,et al.  Crystal Structure of the N-Acetylmannosamine Kinase Domain of GNE , 2009, PloS one.

[54]  L. Pauling,et al.  The structure of proteins; two hydrogen-bonded helical configurations of the polypeptide chain. , 1951, Proceedings of the National Academy of Sciences of the United States of America.