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141.
142.
López-Rodríguez ML Murcia M Benhamú B Viso A Campillo M Pardo L 《Bioorganic & medicinal chemistry letters》2001,11(21):2807-2811
3-D-QSAR/CoMFA methodology and computational simulation of ligand recognition have been successfully applied to explain the binding affinities of a series of benzimidazole derivatives 1-24 acting at serotonin 5-HT(4)Rs. Both derived computational models have facilitated the identification of the structural elements of the ligands that are key to high 5-HT(4)R affinity. The results provide the tools for predicting the affinity of related compounds, and for guiding the design and synthesis of new ligands with predetermined affinities and selectivity. 相似文献
143.
HLA-DM (DM) is a heterodimeric MHC molecule that catalyzes the peptide loading of classical MHC class II molecules in the endosomal/lysosomal compartments of APCs. Although the function of DM is well-established, little is known about how DMalpha and beta-chains fold, oxidize, and form a complex in the endoplasmic reticulum (ER). In this study, we show that glycosylation promotes, but is not essential for, DMalphabeta ER exit. However, glycosylation of DMalpha N15 is required for oxidation of the alpha-chain. The DMalpha and beta-chains direct each others fate: single DMalpha chains cannot fully oxidize without DMbeta, while DMbeta forms disulfide-linked homodimers without DMalpha. Correct oxidation and subsequent ER egress depend on the unique DMbeta C25 and C35 residues. This suggests that the C25-C35 disulfide bond in the peptide-binding domain overcomes the need for stabilizing peptides required by other MHC molecules. 相似文献
144.
145.
One of the fastest growing planktonic species, the salp Thaliademocratica, was analysed for growth rate in three differentoceanic blooms in winter, summer and spring. Each bloom wasmarked by a pair of drogues, and sequentially sampled to obtaina sesies of length frequencies in each population through time.The length frequencies were analysed by an improved method ofmodal analysis. Length-specific growth rate was calculated fromthe progression through time of the resulting series of modes.The blooms showed average growth per individual of 10.4, 14.7and 19.8% in length per hour in winter, summer and spring respectively.These growth rates in the field are compared with growth ratesobtained previously in the laboratory, and the reasons for thevarying estimates of growth rate in the literature are examined. 相似文献
146.
Craig J. Benham 《Cell biochemistry and biophysics》1987,10(3):193-204
The linking difference, α, imposed upon a superhelically constrained DNA molecule must be partitioned between twisting and
bending deformations. Transitions to alternative secondary structures can occur at susceptible sites, altering the local molecular
twist by an amount ΔTw
trans. That part of the linking difference not accommodated in this way, the residual linking difference αres, must be manifested as smooth torsional and flexural deformations of secondary structure. The competition among the alternative
ways of accommodating the imposed linking difference α determines a stressed equilibrium state. The superhelical free energy,G(α), is the excess free energy of the equilibrium state at linking difference α above that of the relaxed state under identical
conditions. In this paper a method is described by which the free energies associated both to linking,G(α), and to residual linking differences can be determined from data on superhelical conformational transitions. The application
of this approach to previously published experimental data on the B-Z transition suggests that the free energy associated
with αres is about 30% larger at substantial superhelicities than it is near the relaxed state. At the onset of transition the functional
form ofG(α) is shown to change in a manner dependent upon the length of the Z-susceptible site. 相似文献
147.
Philip H. Crowley Craig J. Benham Suzanne M. Lenhart Janet L. Morgan 《Journal of theoretical biology》1981,93(4):769-784
The shape and propagation of waves produced by eukaryotic flagella depend on the three-dimensional arrangement and physical-chemical properties of peripheral substructures. The modeling analysis presented here, which assumes force-moment equilibrium and neglects the viscous resistances of the medium, shows how substructural arrangements characteristic of 9+0, 9+1, and 9+2 axonemes can yield their characteristic wave patterns. When flexural stiffnesses are equal along all axonemal radii, any non-uniform doublet shearing pattern propagated distally at constant rate, with successive pairs cycle out of phase, should generate helical waves. When stiffnesses differ greatly on different radii, but the stiffness pattern is the same for all cross-sections, any such shearing pattern should yield planar waves resembling sine-generated curves.Propagated axonemal bending results from the active bending moment produced by local shearing of doublet pairs. Uniformly twisting the doublets about the axonemal axis cannot directly alter the magnitude of the active bending moment. If dynein cross-bridges are activated by shear displacement between peripheral doublets, then the resulting distribution of the active bending moment will be appropriate for balancing the elastic moment in a propagated bending wave. 相似文献
148.
Sequence variation among 10 alleles of the alcohol dehydrogenase (Adh) gene
of the Hawaiian drosophilid D. mimica was analyzed with reference to the
evolutionary history of the Hawaiian subgroup as well as to levels and
patterns of polymorphism of the Adh gene in continental drosophilid
species. The Adh gene of D. mimica is less polymorphic than that of other
drosophilid species, and no replacement substitutions were found.
Statistical analyses of the Adh alleles suggested the action of balancing
selection and revealed significant linkage disequilibrium among three of
the variable sites. The effective population size was estimated to be only
slightly smaller than that of continental species and, surprisingly, on the
same order of magnitude as the actual size.
相似文献
149.
Proteasomes are proteolytic complexes involved in non-lysosomal degradation which are localized in both the cytoplasm and the nucleus. The dynamics of proteasomes in living cells is unclear, as is their targeting to proteins destined for degradation. To investigate the intracellular distribution and mobility of proteasomes in vivo, we generated a fusion protein of the proteasome subunit LMP2 and the green fluorescent protein (GFP). The LMP2-GFP chimera was quantitatively incorporated into catalytically active proteasomes. The GFP-tagged proteasomes were located within both the cytoplasm and the nucleus. Within these two compartments, proteasomes diffused rapidly, and bleaching experiments demonstrated that proteasomes were transported slowly and unidirectionally from the cytoplasm into the nucleus. During mitosis, when the nuclear envelope has disintegrated, proteasomes diffused rapidly throughout the dividing cell without encountering a selective barrier. Immediately after cell division, the restored nuclear envelope formed a new barrier for the diffusing proteasomes. Thus, proteasomes can be transported unidirectionally over the nuclear membrane, but can also enter the nucleus upon reassembly during cell division. Since proteasomes diffuse rapidly in the cytoplasm and nucleus, they may perform quality control by continuous collision with intracellular proteins, and degrading those proteins that are properly tagged or misfolded. 相似文献
150.
This paper develops mathematical methods for describing and analyzing RNA secondary structures. It was motivated by the need to develop rigorous yet efficient methods to treat transitions from one secondary structure to another, which we propose here may occur as motions of loops within RNAs having appropriate sequences. In this approach a molecular sequence is described as a vector of the appropriate length. The concept of symmetries between nucleic acid sequences is developed, and the 48 possible different types of symmetries are described. Each secondary structure possible for a particular nucleotide sequence determines a symmetric, signed permutation matrix. The collection of all possible secondary structures is comprised of all matrices of this type whose left multiplication with the sequence vector leaves that vector unchanged. A transition between two secondary structures is given by the product of the two corresponding structure matrices. This formalism provides an efficient method for describing nucleic acid sequences that allows questions relating to secondary structures and transitions to be addressed using the powerful methods of abstract algebra. In particular, it facilitates the determination of possible secondary structures, including those containing pseudoknots. Although this paper concentrates on RNA structure, this formalism also can be applied to DNA. 相似文献