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Domain modification

Enhanced Pharmaceutical Potential through Domain Modification... [Pg.53]

Figure 7.9 Time-domain representation of an original speech signal (top), and of its time-stretched version (bottom), showing shape invariance. Time-domain modification technique. Figure 7.9 Time-domain representation of an original speech signal (top), and of its time-stretched version (bottom), showing shape invariance. Time-domain modification technique.
The previous section clearly demonstrated the need for CD measurements on a time-resolved basis. Both stopped-flow and chromatographic applications require that CD measurements be obtained on the millisecond, or longer time scale. For this time domain, modification of conventional CD systems is appropriate and this approach has met with excellent success. However, there are a number of important applications where CD information is required in the microsecond to picosecond time domain. Certainly this time regime can not be accessed by simple modification of conventional CD detection strategies and new approaches have therefore been devised to extend CD measurements into the microsecond, and below, time domain. The crux of this section will be to consider CD detection strategies which are designed to improve the measurement SNR, and therefore allow extension into new domains such as time-resolved CD studies. [Pg.35]

Hamon, C., Moulines, E., and Charpentier, F. a diphone synthesis system based on time-domain modifications of speech . In Proceedings of the International Conference on Acoustics Speech and Signal Processing 1989 (1989). [Pg.582]

Very often one single experimental design does not lead to the solution of the problem. In those cases the information obtained at point 5 is used to reformulate the problem (removal of the non-significant variables, redefinition of the experimental domain, modification of the postulated model), after which one... [Pg.27]

In this present investigation, tryptophan residues on the CCBE and CNBE molecule were modified with NBS to assess the role of these residues in catalytic/substrate binding.The results of tryptophan modification by NBS showed that one Trp residue existed in the active site of CCBE s chitosanolytic activity,while two were involved in the active site of its CMCase one located in the substrate binding domain,and the other located in the catalytic domain. Modification of enough Trp residues will lead to the completely loss in both activities of CCBE, suggesting that the tryptophan also help for the stability of enzyme conformation. [Pg.799]

A newer and perhaps more useful application of ellipsometry to Langmuir films is their lateral characterization via ellipsometric microscopy [146], A simple modification of the nuU ellipsometer allows one to image features down to 10-/im resolution. Working with a fixed polarizer and analyzer, some domains are at extinction while others are not and appear bright. This approach requires no fluorescent label and can be applied to systems on reflective supports. [Pg.129]

As already mentioned, the present code corresponds to the solution of steady-state non-isothennal Navier-Stokes equations in two-dimensional Cartesian domains by the continuous penalty method. As an example, we consider modifications required to extend the program to the solution of creeping (Stokes) non-isothermal flow in axisymmetric domains ... [Pg.215]

The HyperChem MMh- code and program also differ from MM2(1977) by having parameters in text files separate from the code. These parameter files are available for your modification and additions. The parameters distributed with HyperChem include the public domain values, generally referred to as the MM2(1991) parameter set, that Dr. Allinger contributed to HyperCube, Inc. Parameters not obtained from Dr. Allinger are appropriately labeled in the distributed parameter files. [Pg.102]

Barium titanate [12047-27-7] has five crystaUine modifications. Of these, the tetragonal form is the most important. The stmcture is based on corner-linked oxygen octahedra, within which are located the Ti" " ions. These can be moved from their central positions either spontaneously or in an apphed electric field. Each TiO octahedron may then be regarded as an electric dipole. If dipoles within a local region, ie, a domain, are oriented parallel to one another and the orientation of all the dipoles within a domain can be changed by the appHcation of an electric field, the material is said to be ferroelectric. At ca 130°C, the Curie temperature, the barium titanate stmcture changes to cubic. The dipoles now behave independentiy, and the material is paraelectric (see Ferroelectrics). [Pg.128]

A closer examination of these essential residues, including the catalytic triad, reveals that they are all part of the same two loop regions in the two domains (Figure 11.10). The domains are oriented so that the ends of the two barrels that contain the Greek key crossover connection (described in Chapter 5) between p strands 3 and 4 face each other along the active site. The essential residues in the active site are in these two crossover connections and in the adjacent hairpin loops between p strands 5 and 6. Most of these essential residues are conserved between different members of the chymotrypsin superfamily. They are, of course, surrounded by other parts of the polypeptide chains, which provide minor modifications of the active site, specific for each particular serine proteinase. [Pg.212]

Ubiquitin modification of substrates can be sensed by proteins, which serve as ubiquitin receptors. These proteins harbor domains capable of ubiquitin binding and help to translate the signal into the proper physiological response by forming signaling complexes or activating downstream effectors. So far more than 15 different ubiquitin recognition motifs have been identified. [Pg.1265]

The above equations gave reasonably reliable M value of SBS. Another approach to modeling the elastic behavior of SBS triblock copolymer has been developed [202]. The first one, the simple model, is obtained by a modification of classical rubber elasticity theory to account for the filler effect of the domain. The major objection was the simple application of mbber elasticity theory to block copolymers without considering the effect of the domain on the distribution function of the mbber matrix chain. In the derivation of classical equation of rabber elasticity, it is assumed that the chain has Gaussian distribution function. The use of this distribution function considers that aU spaces are accessible to a given chain. However, that is not the case of TPEs because the domain also takes up space in block copolymers. [Pg.138]

Styrene-butadiene-styrene (SBS) block copolymers are adequate raw materials to produce thermoplastic mbbers (TRs). SBS contains butadiene—soft and elastic—and styrene— hard and tough—domains. Because the styrene domains act as cross-links, vulcanization is not necessary to provide dimensional stability. TRs generally contain polystyrene (to impart hardness), plasticizers, fillers, and antioxidants processing oils can also be added. Due to their nature, TR soles show low surface energy, and to reach proper adhesion a surface modification is always needed. [Pg.762]


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See also in sourсe #XX -- [ Pg.53 ]




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