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Structural enzyme reaction mechanism studies

Although experimental studies provide significant amounts of information regarding the structure and the catalytic activity of these enzymes, several issues concerning the structure (presence of water in the active site) and the catalytic mechanism remained unresolved. Based on the complete X-ray structure of human plasma GPx (2.9 A resolution) [64], we performed active-site and ONIOM QM MM calculations of structure and reaction mechanism [27, 28, 65],... [Pg.39]

Alcohol dehydrogenases are enzymes that are well known from physiological and biochemical studies on the primary metabolism of cells. Several ADHs are commercially available and for some of them such as the ADH from yeast or liver details concerning the structure and reaction mechanism have been elucidated. For preparative applications however they seldom meet the requirements and new enzymes are needed for this field. [Pg.148]

The mechanism of oxygen activation by P-450 has been extensively studied (7c, 5a, b) however, cmcial intermediates in the catalytic cycle are so unstable that it is not possible to examine their structures and reactivities. Accordingly, model systems for P-450 with synthetic metalloporphyrins have illuminated the enzymic reaction mechanism. For instance, the so-called picket fence porphyrin, /ncjo-tetra(a,a,a,a-pivalamidophenyl)porphyrin (TpivPP) Fe(II), prepared by Collman and co-workers, forms a stable complex with O2 6a, b). An X-ray... [Pg.406]

Although soluble methane monooxygenases (sMMO) located in the cytoplasm of the bacterial cells have been well characterized in terms of their structure and reaction mechanism, " those of pMMO and AMO are poorly understood at present. This is due to difficulty in obtaining a pure enzyme that retains reactivity. It has so far been demonstrated that the enzymes contain up to 15 copper ions per enzyme, but only a type 2 copper(II) supported by three or four imidazole ligands can be detected by The X-ray absorption and EPR studies... [Pg.375]

A variety of techniques have been applied to investigate enzyme reaction mechanisms. Kinetic and X-ray crystallographic studies have made major contributions to the elucidation of enzyme mechanisms. Valuable information has been gained from chanical, spectroscopic and biochemical studies of the transition-state structures and intermediates of enzyme catalysis. Computational studies provide necessary refinement toward our understanding of enzyme mechanisms. The ability of an enzyme to accelerate the rate of a chemical reaction derives from the complementarity of the enzyme s active site structure to the activated complex. The transition state by definition has a very short lifetime ( 10 s). Stabilization of the transition state alone is necessary but not sufficient to give catalysis, which requires differential binding of substrate and transition state. Thus a detailed enzyme reaction mechanism can be proposed only when kinetic, chemical and structural components have been studied. The online enzyme catalytic mechanism database is accessible at EzCatDB (http //mbs.cbrc.jp/EzCatDB/). [Pg.344]

Kinetics is the branch of science concerned with the rates of chemical reactions. The study of enzyme kinetics addresses the biological roles of enzymatic catalysts and how they accomplish their remarkable feats. In enzyme kinetics, we seek to determine the maximum reaction velocity that the enzyme can attain and its binding affinities for substrates and inhibitors. Coupled with studies on the structure and chemistry of the enzyme, analysis of the enzymatic rate under different reaction conditions yields insights regarding the enzyme s mechanism of catalytic action. Such information is essential to an overall understanding of metabolism. [Pg.431]

Sjbberg B-M (1997) Ribonucleotide Reductases - A Group of Enzymes with Different Metallosites and a Similar Reaction Mechanism. 88 139-174 Slebodnick C, Hamstra BJ, Pecoraro VL (1997) Modeling the Biological Chemistry of Vanadium Structural and Reactivity Studies Elucidating Biological Function. 89 51-108 Smit HHA, see Thiel RC (1993) 81 1-40... [Pg.255]

In this chapter we have seen that enzymatic catalysis is initiated by the reversible interactions of a substrate molecule with the active site of the enzyme to form a non-covalent binary complex. The chemical transformation of the substrate to the product molecule occurs within the context of the enzyme active site subsequent to initial complex formation. We saw that the enormous rate enhancements for enzyme-catalyzed reactions are the result of specific mechanisms that enzymes use to achieve large reductions in the energy of activation associated with attainment of the reaction transition state structure. Stabilization of the reaction transition state in the context of the enzymatic reaction is the key contributor to both enzymatic rate enhancement and substrate specificity. We described several chemical strategies by which enzymes achieve this transition state stabilization. We also saw in this chapter that enzyme reactions are most commonly studied by following the kinetics of these reactions under steady state conditions. We defined three kinetic constants—kai KM, and kcJKM—that can be used to define the efficiency of enzymatic catalysis, and each reports on different portions of the enzymatic reaction pathway. Perturbations... [Pg.46]

Zhang Y, Kua J, McCammon JA (2003) Influence of structural fluctuation on enzyme reaction energy barriers in combined quantum mechanical/molecular mechanical studies. J Phys Chem B 107 ... [Pg.349]


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See also in sourсe #XX -- [ Pg.344 ]




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