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Physiological function kinetic properties

Thus, there is likely as many as three enzymes with 5 -nucleotidase activity in liver, one lysosomal, one cytoplasmic, and one membrane bound. Their specificities and kinetic properties appear to be distinctly different. This would suggest specialized physiological functions not yet understood. [Pg.345]

The specific system that we use to explore these questions is the conventional myosin, also termed myosin 11, which plays key physiological functions in muscle contraction and cell division. It is an ideal system for in-depth theoretical and computational analysis because its structural and kinetic properties have been characterized by a large body of diverse experimental techniques." For example, at the time our research was initiated, myosin 11 was one of the few motor systems for which high-resolution x-ray structures are available for multiple functional states " since then, multiple high-resolution x-ray structures have also been obtained for myosin V and VI, two other widely studied members of the myosin superfamily that are more processive in nature compared to myosin 11. The functional cycle of myosin 11 is best described by the celebrated Lymn-Taylor schane (Figure 2.1a)," in which... [Pg.24]

The sequences of biochemical transformations involved in the synthesis of the aspartate family and branched-chain amino acids in multicellular plants are similar to those that occur in microorganisms. Support for this conclusion has been derived principally from isolation of a number of the requisite enzymes. Information on the kinetic and physical properties of enzymes is best achieved after extensive purification. In contrast, useful predictions of the physiological function of regulatory enzymes depend upon effective enzyme extraction and complete preservation of native properties. Since the latter objective has been emphasized during most investigations of enzymes associated with amino acid biosynthesis in plants, the bulk of our knowledge has been obtained from comparatively crude enzyme preparations. Results of both direct and competitive labeling experiments have added demonstrations of many of the predicted precursor-product relationships and a few metabolic intermediates have been isolated from plants. The nature of a number of intermediate reactions does, however, remain to be clarified notably, the reactions associated with the conversion of dihydropicolinate to lysine and those involved in the synthesis of leucine from 2-oxoisovalerate. [Pg.447]

Note that Eq. (6) includes thermodynamic equilibrium (v° = 0) as a special case. However, usually the steady-state condition refers to a stationary nonequilibrium state, with nonzero net flux and positive entropy production. We emphasize the distinction between network stoichiometry and reaction kinetics that is implicit in Eqs. (5) and (6). While kinetic rate functions and the associated parameter values are often not accessible, the stoichiometric matrix is usually (and excluding evolutionary time scales) an invariant property of metabolic reaction networks, that is, its entries are independent of temperature, pH values, and other physiological conditions. [Pg.122]

This review is concerned with the chemical and physical properties of proteins and enzymes containing three distinct and unique forms of Cu The "blue center or, in the nomenclature proposed by Vdnng rd, Type 1 Cu2+ the colorless or Type 2 Cu2+, common to all multi-copper oxidases which reduce molecular oxygen to two molecules of water and the Cu associated with the 330 nm absorption band, again common to the oxidases. The purposes of the review are to assemble chemical and physical data related to the indicated types of Cu binding sites, to offer some interpretations (and occasionally re-interpretations) of experimental results concerned with structure-function relationships, and to generalize some of the information available as it concerns the structures of these unique Cu-co-ordination complexes. Special emphasis will be placed on the kinetic and mechanistic work which has been carried out on the multi-copper oxidases while the physiological roles of the various protein systems will not be of particular importance. [Pg.2]


See other pages where Physiological function kinetic properties is mentioned: [Pg.274]    [Pg.283]    [Pg.36]    [Pg.616]    [Pg.28]    [Pg.46]    [Pg.1873]    [Pg.120]    [Pg.225]    [Pg.2]    [Pg.2]    [Pg.449]    [Pg.225]    [Pg.1872]    [Pg.284]    [Pg.45]    [Pg.225]    [Pg.8]    [Pg.489]    [Pg.164]    [Pg.521]    [Pg.151]    [Pg.119]    [Pg.321]    [Pg.310]    [Pg.131]    [Pg.131]    [Pg.170]    [Pg.407]    [Pg.465]    [Pg.359]    [Pg.140]    [Pg.144]    [Pg.357]    [Pg.32]    [Pg.424]    [Pg.254]    [Pg.188]    [Pg.243]    [Pg.149]   
See also in sourсe #XX -- [ Pg.467 , Pg.468 , Pg.469 ]

See also in sourсe #XX -- [ Pg.467 , Pg.468 , Pg.469 ]




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