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A Functional Model

Kainer R. A functional model of the rat kidney. J Math Biol 1979 7 57-94. Kassissia IG, Goresky CA, Rose CP, Schwab AJ, Simard A, Huet PM, Bach GG. Tracer oxygen distribution is barrier-limited in the cerebral microcirculation. Circ Res 1995 77 1201-11. [Pg.526]

Collman JP, Fu L, Herrmann PC, Zhang X. 1997. A functional model related to C3ftochrome c oxidase and its electrocatal34ic four-electron reduction of O2. Science 275 949. [Pg.688]

Collman JP, Sunderland CJ, Berg KE, Vance MA, Solomon El. 2003c. Spectroscopic evidence for a heme-superoxide/Cu(I) intermediate in a functional model of cytochrome c oxidase. J Am Chem Soc 125 6648. [Pg.688]

Fig. 6.22 A function model of the sodium channel. P denotes protein, S the potential sensitive sensor and H the gate. The negative sign marks the carboxylate group where the guanidine group of tetro-dotoxin can be attached. (According to B. Hille)... Fig. 6.22 A function model of the sodium channel. P denotes protein, S the potential sensitive sensor and H the gate. The negative sign marks the carboxylate group where the guanidine group of tetro-dotoxin can be attached. (According to B. Hille)...
Corwin, D.L., Waggoner, B.L. and Rhoades, J.D. (1991) A Functional Model of Solute Transport that Accounts for Bypass, J. Environ. Qual. 20, 647-658. [Pg.590]

Itoh et al. used Cu yd-diketiminato complexes with general formula 4, and their reactivity has been described as a functional model for pMMO (particulate methane monooxygenase). Initially, the Hgands were reacted with both Cu and Cu precursors, with a variety of species formed, depending on the specific conditions employed [111, 112]. It was then shown that both Cu and Cu complexes ultimately led to bis(/z-oxo)(Cu )2 species upon reaction with O2 and H2O2, respectively. Use of these Cu complexes as the pre-catalysts for the oxidation of alkanes (cyclohexane and adamantane) in the presence of H2O2 resulted in low yields ( 20%). [Pg.33]

Fukuzumi and Itoh have jointly reported on a if-peroxo dicop-per(ll) complex that acts as a functional model for the phenolase activity of tyrosinase. lithium salts of para-substituted phenols were used as substrates, reaching yields between 60 and 90% with only the catechol product formed... [Pg.52]

For a large class of signals, therefore, the sine-wave analysis/synthesis is nearly a perceptual identity system and the signals are expressed in terms of a functional model describing the behavior of each of its sine-wave components. The sine-wave representation therefore provides an appropriate framework for developing signal modification and enhancement techniques based on transforming each of the functional descriptors. [Pg.197]

Figure 3-24. A zinc(ii) complex which acts as a functional model for the hydride transfer reaction which occurs at the active site of the enzyme liver alcohol dehydrogenase. Figure 3-24. A zinc(ii) complex which acts as a functional model for the hydride transfer reaction which occurs at the active site of the enzyme liver alcohol dehydrogenase.
A (generally intermolecular) system that carries out the reaction concerned without the binding characteristics of the enzyme. This may be termed a functional model. [Pg.812]

From your reading of Chapters 2 and 12, suggest desirable characteristics that might be exhibited by (a) a structural model and (b) a functional model for haemoglobin. [Pg.857]

Liu, J. G., Naruta, Y., Tani, F., A functional model of the cytochrome c oxidase active site Unique conversion of a heme-mu-peroxo-Cu-II intermediate into heme-superoxo/Cu-I. Angew. Chem., Int. Ed. 2005, 44, 1836-1840. [Pg.859]

Murakami et al. [19] developed an additional vitamin B6 model system with a binding site. They synthesized an octopus cyclophane (27) as a functional model of the protein matrix of transaminase. This cyclophane formed a hydrophobic cavity in water where PLP could be noncovalendy incorporated. Alkylamines having various hydro-phobic chains were employed as substrates, in place of a-amino adds, to evaluate the hydrophobic effect on the Schiff base-forming equilibrium. The Schiff base formation constant was found to depend markedly on the chain length of a substrate in the presence of 27, indicating that the octopus cyclophane can be utilized as an effective ho-loenzyme model capable of forming a ternary complex. [Pg.45]

Limburg J, Vrettos JS, Liable-Sands LM, Rheingold AL, Crabtree RH, Brudvig GW. A functional model for 0-0 bond formation by the O2 evolving complex in photosystem II. Science. 1999 283(5407) 1524-7. [Pg.218]

A Functional Model for Copper Monooxygenases and the NIH Shift Mechanism... [Pg.182]

A Functional Model for 0-0 Bond Formation by the 02-Evolving Complex in Photosystem II , Julian Limburg, John S. Vrettos, Louise M. Liable-Sands, Arnold L. Rheingold, Robert H. Crabtree and Gary W. Brudvig (1999) Science 283, 1524-1527. [Pg.61]

The binuclear Cu/Co compound (17-F-VI) acts as a functional model for cytochrome c oxidase. The natural enzyme contains a copper atom coordinated to... [Pg.828]

FIGURE 7. A functional model for galactose oxidase (Wang et cd., 1998). [Pg.195]

Develop a Functional Model of the System (Function Diagram)... [Pg.85]

The control of normal motor behaviour is under influence of the basal ganglia through a so-called reinforcing basal ganglia-thalamocortical motor circuit . Based on current data from a variety of experimental fields, a functional model of this motor circuit has been proposed, as depicted, greatly simplified, in Figure 1.2. [Pg.16]

The first use of a porphyrin as a functional model for cytochrome P-450 was the seminal work of the group of Groves [296] in which an Fe(III) porphyrin was used with lodosylbenzene. The success of this early work led to the development of what has been described as three generations of catalysts [521], and here expanded to four generations, based on metallotetraarylporphyrins which differ on the degree of substitution in the rings (Fig. 1.23). [Pg.61]

K. Chen, L. Que Jr., czs-Dlhydroxylation of olefins by a nonheme iron catalyst. A functional model for Rieske dioxygenases, Angew. Chem. Int. Ed. Engl. 38 (1999) 2227. [Pg.83]

Fig. 6. Cytochrome bS59 photooxidation in spinach chioropiasts (A), photoreduction in TSF2a particles (B) and in D1/D2/Cyt bS59 complex (C). See text for discussion. Figure (A) from Knaff and Arnon (1969) Light-induced oxidation of chloroplast b-type cytochrome at-189 °C. Proc Nat Acad Sci, USA 63 959, 960 (B) Ke, Vernon and Cheney (1972) Photoreduction of cytochrome b5S9 in a photosystem-ll subchloroplast particle. Biochim Biophys Acta 256 350 (C) Barber and De Las Rivas (1993) A functional model for the role of cytochrome (3559 in the protection against donor and acceptor side photoinhibition. Proc Nat Acad Sci, USA 90 10943, 10944. Fig. 6. Cytochrome bS59 photooxidation in spinach chioropiasts (A), photoreduction in TSF2a particles (B) and in D1/D2/Cyt bS59 complex (C). See text for discussion. Figure (A) from Knaff and Arnon (1969) Light-induced oxidation of chloroplast b-type cytochrome at-189 °C. Proc Nat Acad Sci, USA 63 959, 960 (B) Ke, Vernon and Cheney (1972) Photoreduction of cytochrome b5S9 in a photosystem-ll subchloroplast particle. Biochim Biophys Acta 256 350 (C) Barber and De Las Rivas (1993) A functional model for the role of cytochrome (3559 in the protection against donor and acceptor side photoinhibition. Proc Nat Acad Sci, USA 90 10943, 10944.

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