Tridimensional structure

Figure 10.9 Tridimensional structure of GM-CSF.148 The tridimensional structure shows that the four methionine residues present on the molecule have different degrees of solvent exposure. The sulfur atoms are either fully exposed (residues M46 and M79), partially exposed (residue M36), or totally buried (residue M80). Forced oxidation experiments described in the text show that residue M80 is unaffected, whereas local structural constraints make M79 less susceptible to oxidation than predicted by the model. [Pg.261]

To approach the complexity of a real tridimensional structure, let us first consider the case of a monodimensional array of alternating positive and negative charges, each at distance r from its first neighbor. We will assume for the sake of simplicity that the dispersive potential is negligible. The total potential is therefore... [Pg.45]

Fig. 9. Cucurbituril inclusion chemistry (a) tridimensional structure of cucurbit[6]uril (b) conjectured cross-sectional representation of a host—guest...

Flavonoids bear different degrees of hydroxylation, polymerization, and methylation that define both specific and nonspecific interactions with membrane lipids. Molecule size, tridimensional structure, and hydrophili-city/hydrophobicity are chemical parameters that determine the nature and extent of flavonoid interactions with lipid bilayers. The hydrophilic character of certain flavonoids and their oligomers endows these molecules with the ability to bind to the polar headgroups of lipids localized at the water-lipid interface of membranes. On the other hand, flavonoids with hydrophobic character can reach and cross the lipid bilayer. In this section, we will discuss current experimental evidences on the consequences of flavonoid interactions with both the surface and the hydrophobic core of the lipid bilayer. [Pg.108]

Furthermore, the models have to be reproducible. The model should give the same result when used by different users in different locations. This fact may lead to a preference toward easier models. Depending on the method for QS AR, some steps may be critical for reproducibility. Indeed, some approaches require manual optimization of the tridimensional structure of the chemical, e.g., in the case of tridimensional descriptors. In other cases, stochastic processes are used. Some more complex models done by skilled operators, such as docking, can be critical. Another source of variability is the software version or brand, even for simple bidimensional descriptors. [Pg.192]

Chemical descriptors are in most of the cases obtained with equations that are not known. Even if the references to certain general equations are given, in practice, it is difficult to replicate the results obtained with chemical descriptors. As we have discussed, chemical descriptors based on tridimensional structures are subject to manual optimization, and this may change the descriptor values. But even in the case of other simpler descriptors, we found that using software from two different commercial sources, the results may be different. Even the use of two different versions of the same software may provide different results for the same descriptor. Even descriptors, which seem simple, such as number of double bonds, or of aromatic rings, are critical because they depend on how tautomers and aromaticity are considered in the different software, or are sensitive to the structure format that is used. [Pg.198]

Figure 9.1 shows the tridimensional structure of chloroperoxidase where some potential modification sites are marked. These include side chains of amino acids such as lysine, histidine, and aspartic acid, as well as the propionates from the heme group and carbohydrate moieties. To illustrate how enzyme technology has impacted the development of biocatalysts based on peroxidases, we highlight important aspects described in literature immobilization, chemical and genetic modification of peroxidases. [Pg.219]

The molecular architecture of glucoamylase permits some interesting hypotheses to be made in relation to the tridimensional structure of enzymes. As indicated in the preceding Section, this enzyme possesses many short, oligosaccharide moieties attached along its polypeptide chain. It is possible that the spacing of the fragments... [Pg.327]

The crystal structures of many compounds are dominated by the effect of H-bonds, as, for example, in the case of the tridimensional structure of ice, the layer structure of B(OH)3, and the infinite zig-zag chains in crystalline HF. [Pg.319]

S Non-covalent Protein Complexes and Tridimensional Structural Information... [Pg.336]

Mass spectrometry also provides information on the tridimensional structure of proteins. Often, the information from mass spectrometry complements those obtained by other techniques such as circular dichroism, nuclear magnetic resonance or fluorescence. In some circumstances, mass spectrometry, by its speed and sensitivity, allows information to be obtained that is impossible to obtain by other techniques. [Pg.338]

Imberty, A Chanzy, H., Perez, S., Buleon, A., and Tran, V. 1987. New tridimensional structure for A-type starch. Macromolecules 20, 2634-2636. [Pg.180]

Intermediate filaments are about lOnm in diameter, and are more stable (strongly bound) than actin filaments. Like actin filaments they function in the maintenance of cell shape by bearing tension. Intermediate filaments organise the internal tridimensional structure of the ceU, anchoring organelles and serving as structural components of the nuclear lamina (a dense fibrillar network inside the nucleus) and sarcomeres. They also participate in some cell-cell and cell-matrix junctions. [Pg.273]

A different path occurs with very little weight loss, leads to more oxidatively stable materials, and keeps the tridimensional structure of the resin. The reactions taking place in this path are shown below ... [Pg.627]

It is important to note that the cases of metal crystallites on a substrate and of a substrate of arbitrary thickness deposited upon a metal foil are not equivalent from a thermodynamic point of view because the constraints to which each of these systems are subjected are different. In the first case, a monolayer of TiOx will cover the metal, the amount being determined by the equilibrium with the surface of the substrate. For the second, the entire deposit of TiC>2 must be located on the surface. Since the coverage by a monolayer leads to the smallest free energy, the excess of TiOx should form in the latter case a tridimensional structure with the least possible surface area over the smallest possible part of the substrate surface, thus minimizing the free energy. There are, however, kinetic difficulties to achieve such a structure. For this reason, if coo<0, it is likely that a metastable state of extended patches... [Pg.163]

Below here we will focus on an original computational method that accounts for the experimentally observed radioprotection of the partners in DNA-protein complexes. Validated by comparison between experiment and calculation, it can be used to predict the damage extent and distribution in any biomolecule or complex of biomolecules whose tridimensional structure is known. [Pg.266]

The RADACK (contraction of RADiation-induced attACK) model, that we have developed [9,10], accounts for the experimentally determined probabilities of radiolytic damages caused by the OH radical attack in all forms of DNA (B [11], Z [12], triplex [13], quadruplex [14]), in DNA-protein complexes [15] and has the potential to predict radiolytic attack probabilities in other molecules or assemblies. Direct ionisation effects are not taken into account. The determination of relative probabilities of reaction ofthe target with the OH radicals takes into account two factors 1) the accessibility of the reactive sites of the target since it uses the exact tridimensional structure of the macromolecule or assembly as determined by NMR, crystallography or as built up by molecular modelling, and 2) the chemical reactivity of the residues (nucleotides or amino-acids). [Pg.267]

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