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Complex function residue

Each food or food ingredient shows a characteristic equiHbrium relative humidity at a given moisture content and temperature. Thus as a food is dried and its moisture content is reduced from its fresh value where water activity is generally 1.0, to lower and lower values, the equiHbrium water activity of the food decreases as a complex function of residual moisture. The shape of the equiHbrium relative humidity—moisture content curve is set by the chemistry of the food. Foods high ia fmctose, for example, biad water and thus show lower water activities at high moisture contents. Dried pmnes and raisias are examples. Drying can be terminated at any desired moisture content and hence any water activity. [Pg.460]

The size and complexity of the motif is clearly important, single hehces are of limited use because of the long intra-residue distances on the helical surface (Fig. 2) and functions that require more than two-residue sites will most hkely have to depend on the functionahzation of supersecondary structures. The clever designs of catalysts for decarboxylation and hgation reactions are, on the other hand, good examples of how small motifs can be exploited for complex functions [11,12]. [Pg.59]

While membrane anchors normally contain nonpolar residues, not all transmembrane a-helices act as membrane anchors. Some transmembrane helices have a more complex functional role than serving as a simple tether. Some helices aggregate within a membrane to create a channel. The channel allows the passage of ions across an otherwise impermeable membrane. Many proteins form ion channels, and most use helices to form the breach in the cell membrane. [Pg.67]

Analysis of pseudorevertants (or suppressor) of unc mutants is a unique approach to find functional and/or structural interactions) between the two amino acid residues in the complex enzyme. Residues near the -y-phosphate moiety of ATP could be mapped relative to the residues in the glycine-rich sequence by identifying pseudorevertants of the mutants in the glycine-rich sequence. Conversely, other residues can also be mapped closely to the glycine-rich sequence, if effects of their mutations are suppressed by mutations in the glycine-rich sequence. [Pg.220]

The membrane protein is stably buried in the Hpid bilayer due to the amphiphilic nature of the membrane protein. The surfaces of some parts of the protein have mainly hydrophobic amino acid residues, and hydrophihc residues are located on the other surfaces. The former parts are accommodated in the hydrophobic lipid bilayer and the latter protein regions are exposed to the surface of the water. Membrane proteins work as receptors, channels and so on. Specific interactions between these proteins lead to complex functions such as signal transduction and energy conversion. Many of the functions expressed by the cell membrane can be attributed to the functionality of the membrane proteins. [Pg.178]

To determine whether inhibitors specifically inhibit the PTP of interest in primary human T cells, purified T cells can be used, in which the target PTP has been acutely eliminated (residual expression <20 % of normal expression) by short interfering RNA (siRNA)- or small hairpin RNA (shRNA)-mediated knockdown. Signaling in T cells with severely reduced protein levels of the PTP of interest is expected to be similar to signaling in T cells treated with a specific inhibitor of the PTP. However, this may not always be the case. Inhibition of PTP activity by the inhibitor, or eliminating the protein altogether via RNAi, may have different outcomes due to a more complex function of the PTP that is not based on its phosphatase activity alone [31]. Nonetheless, the combined action of PTP inhibitor and PTP knockdown should not alter signaling beyond what is observed for each alone. [Pg.261]

Transmission electron microscopy (TEM) images showed that GNPs conjugated with Tat peptide (nuclear localization sequence) were mainly located in the nucleus of fibroblast and also revealed no appreciable cytotoxic effects [22]. In contrast, Tkachenko et al. functionalized GNPs with four different nuclear localization peptides ending with a Cys residue (which contains a free thiol) to evaluate the cellular trajectories of peptide gold complexes. Functionalized GNPs were... [Pg.53]

The bottom residues from DMT fabrication are benzyl and methyl esters of dicarboxylic and tricarboxylic acids with biphenyl or triphenyl structures together with DMT [4, 6. By the transesterification reactions of these complex ester residues with diethyleneglycol (DEG), aromatic polyester polyols with a functionality in the range 22-23 OH groups/mol are obtained. [Pg.421]

The degree of couplii attained is a complex function of reactirm variables Functionality increases as precursor mdecular weight is decreased, as total polymer concentration is increased or as tibe amount of divinylbenzene is increased. The quantity of residual precursor mrdecules in the product is usually low (<3%) and dthou the sanqples produced by this method are probably not as monod perse as indicated by s( dusticated fractirmation techniques due to difficulties in separation of branched prdymers of high molecular weight, Mw/M is likely to be less than 1.3. It is in any case the (mly method available for the production of star macromolecules of high fimctionality and is useful for the preparation of macromolecules of functionality between six and twenty. [Pg.93]

Unfortunately, residual baseline anomalies are not often simple offsets or linear slopes, but are more complex functions. [Pg.226]

The influence of modulated hold pressure on the sprue solidification time and quality of mouldings has been demonstrated with silicon nitride and silicon suspensions and a rotor mou1d 2 An increase in pressure amplitude was found to eliminate cracks in the moulded state and rotors could be heated near to the softening point of the suspension without the appearance of cracks. At very high pressure amplitudes cracks again appeared. Clearly the residual stress distribution is a complex function of pressure amplitude and at present can only be adjusted empirically. The combined effect of mould temperature adjustment and modulated hold pressure has shown how sprue solidification can be adjusted and it also allowed an... [Pg.238]


See other pages where Complex function residue is mentioned: [Pg.375]    [Pg.326]    [Pg.79]    [Pg.106]    [Pg.189]    [Pg.126]    [Pg.385]    [Pg.110]    [Pg.229]    [Pg.240]    [Pg.571]    [Pg.223]    [Pg.776]    [Pg.366]    [Pg.1079]    [Pg.543]    [Pg.82]    [Pg.5]    [Pg.42]    [Pg.105]    [Pg.274]    [Pg.385]    [Pg.91]    [Pg.376]    [Pg.621]    [Pg.718]    [Pg.418]    [Pg.173]    [Pg.177]    [Pg.78]    [Pg.353]    [Pg.156]    [Pg.447]    [Pg.505]    [Pg.1775]    [Pg.2462]    [Pg.269]    [Pg.133]    [Pg.98]   
See also in sourсe #XX -- [ Pg.382 ]

See also in sourсe #XX -- [ Pg.382 ]




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Complex functions

Residual function

Residual function surface complexation calculations

Residues function

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