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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Proteins: Structure, Function, and Genetics 27 (1997), S. 545-555 
    ISSN: 0887-3585
    Keywords: semi-empirical ; PM3 method ; quantum mechanics ; molecular mechanics ; reaction pathway ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Different pathways of the metal-induced isomerization of D-xylose to D-xylulose are investigated and compared in detail using energy minimization and molecular dynamics simulation. Two theoretical models are constructed for the reaction: in vacuum and in the enzyme D-xylose isomerase. The vacuum model is constructed based on the X-ray structure of the active site of D-xylose isomerase. It contains the atoms directly involved in the reaction and is studied using a semi-empirical molecular orbital method (PM3). The model in the enzyme includes the effects of the enzyme environment on the reaction using a combined quantum mechanical and molecular mechanical potential. For both models, the structures of the reactants, products, and intermediate complexes along the isomerization pathway are optimized. The effects of the position of the “catalytic Mg2+ ion” on the energies of the reactions are studied. The results indicate: 1) in vacuum, the isomerization reaction is favored when the catalytic metal cation is at site A, which is remote from the substrate; 2) in the enzyme, the catalytic metal cation, starting from site A, moves and stays at site B, which is close to the substrate; analysis of the charge redistribution of the active site during the catalytic process shows that the metal ion acts as a Lewis acid to polarize the substrate and catalyze the hydride shift; these results are consistent with previous experimental observations; and 3) Lys183 plays an important role in the isomerization reaction. The ε-NH3+ group of its side chain can provide a proton to the carboxide ion of the substrate to form a hydroxyl group after the hydride shift step. This role of Lys183 has not been suggested before. Based on our calculations, we believe that this is a reasonable mechanism and consistent with site-directed mutation experiments. © 1997 Wiley-Liss Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemistry - A European Journal 2 (1996), S. 191-195 
    ISSN: 0947-6539
    Keywords: computer simulations ; molecular dynamics ; nucleophilic substitutions ; quantum chemistry ; solvent effects ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Solvent effects on an SN2 reaction at nitrogen (Cl- + NH2Cl → ClNH2 + Cl-) in dimethyl ether solution were studied by means of molecular dynamics simulation with a combined quantum-chemical and molecular-mechanical potential. The energetics and geometrical parameters of the reaction in the gas phase, calculated by means of the semiempirical model PM3(the quantum chemical part of the combined potential), were compared with ab initio calculations up to the 6-311 + G* */MP2 and 6-311 + G(2 d,p)/MP2 levels of theory. Compared with the gas phase potential energy surface, the free energy profile of the reaction in dimethyl ether solution shows that the solvent makes the ion-dipole complex well shallower by approximately 6.4 kcal mol-1 and raises the height of the effective barrier from the complex to the transition state by about 2.2 kcal mol-1. The overall transition barrier between the separated reactants and the products is raised from 6.4 kcal mol-1 to 15.0 kcal mol-1 upon solvation. The radial distribution functions between solvent-solute atom pairs at different stages of the reaction course were compared. Results show that better solvation of the charge-localised separated reactants is responsible for the increase in the barrier height. Polarisation of the solute by its surroundings is also discussed.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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