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Associated base pairs

Pvrimidine Hetero-Association Base-Pair Configurations with Purine-ry... [Pg.263]

Differences in the capacity of inhibition by polynucleotides not involved in complementary hydrogen bonds and by double-helical complexes of synthetic polyribonucleotides, or double-stranded viral RNA allow the conclusion that it is above all the regions of associated base pairs which are recognized in the RNA by anti-poly I poly C antibodies. Such complementary double-stranded helical regions have been described especially in tRNA but they have also been shown to exist in ribosomal RNA. These two kinds of RNA were therefore isolated and studied separately. Although both fractions precipitate anti-poly I poly C antibodies, their reactivity is nevertheless very different and rRNA precipitates eight times as much antibody as tRNA. Since tRNA possesses an important tertiary structure, this low reactivity could be explained by the non-accessibility of antigenic sites. [Pg.16]

V (the potential) is identified with the enthalpy, i.e. the number n of base pairings (contacts), and T corresponds to the entropy. At each stage in the folding process, as many as possible new favourable intramolecular interactions are fonned, while minimizing the loss of confonnational freedom (the principle of sequential minimization of entropy loss, SMEL). The entropy loss associated with loop closure is (and the rate of loop closure exp... [Pg.2821]

The DNA base pairs guanine (G), cytosine (C), adenine (A) and thymine (T). The uracil-2,6-diaminopyridine pair can also form three hydrogen bonds but has a much lower association constant than G-C. [Pg.245]

Dou ble hel ix (Section 28 8) The form in which DNA normally occurs in living systems Two complementary strands of DNA are associated with each other by hydrogen bonds be tween their base pairs and each DNA strand adopts a helical shape... [Pg.1281]

The authors claim that these associations, which are destroyed in fixed compounds, play an important role in the calculation of Ty.The cases of 1,2,4-triazole-5-thiones 74 [97SA(A)699] and of pyridone dimers 15a-15a and 15a-15b were also studied [96MI(13)65]. (3) The recording of IR spectra in solution at different temperatures to determine the effect of the temperature on Kj-, for instance, in pyrazolinones [83JPR(325)238] and in cytosine-guanine base pairs [92MI(9)881]. (4) The determination of the equilibrium 2-aminopyridine/acetic acid 2-aminopyridinium acetate (see Section III.E) in the acid-base complex was carried out by IR (97NKK100). [Pg.48]

Fig. 3.18 Nucleosome core particle (NCP)-polyamide co-crystal structures (PDB codes 1M18 and 1M19). (Top) Partial structure, viewed down the superhelical axis. Base pairs 58-145 (shown in white) and associated proteins (H3, blue H4, green H2A, yellow H2B, red) are shown for each complex. Superhelix locations (SHLs) are labeled as each major... Fig. 3.18 Nucleosome core particle (NCP)-polyamide co-crystal structures (PDB codes 1M18 and 1M19). (Top) Partial structure, viewed down the superhelical axis. Base pairs 58-145 (shown in white) and associated proteins (H3, blue H4, green H2A, yellow H2B, red) are shown for each complex. Superhelix locations (SHLs) are labeled as each major...
Lee et al. [60] investigated the adhesion of a single pair of DNA strands. They identified two types of forces interchain forces associated with Watson-Crick base pairing between complementary strands, and intrachain forces associated with the elasticity of single strands. For studying interchain interactions, complementary oligomers (ACTG)s and... [Pg.38]

Figure 36-25. Double-strand break repair of DNA. The proteins Ku and DNA-dependent protein kinase combine to approximate the two strands and unwind them. The aligned fragments form base pairs the extra ends are removed, probably by a DNA-PK-associated endo- or exonuclease, and the gaps are filled in and continuity is restored by ligation. Figure 36-25. Double-strand break repair of DNA. The proteins Ku and DNA-dependent protein kinase combine to approximate the two strands and unwind them. The aligned fragments form base pairs the extra ends are removed, probably by a DNA-PK-associated endo- or exonuclease, and the gaps are filled in and continuity is restored by ligation.
Binding of berberine caused changes in the circular dichroic spectrum of all B-DNAs with an increase of molar ellipticity of the 270 nm band the molar ellipticity value at saturation depended strongly on the base composition of DNA being larger for the AT-rich DNA than the GC-rich DNA. However, the generation of berberine-associated extrinsic circular dichro-ism bands was not dependent on the base composition or sequence of base pairs. [Pg.178]

Significantly, it has been shown that coordination of nucleobases can enhance base pairing interactions (115). These findings confirm previous theoretical calculations (116). The association constant for Watson-Crick interactions between 9-EtG and 1-MeC was 6.9 M 1, determined... [Pg.120]

Metal-modified base pairs have been reported some time ago for identical (119), complementary (120), and non-complementary bases (59,121-126). These may assemble into a type I quartet through dimerization, as seen for trassociation constant of 59.1 M 1 in d6-DMSO (123). Rather unusual is the involvement of the aromatic C-H5 proton in the hydrogen bond-... [Pg.121]

Single nucleotide polymorphisms Single base-pair changes that are inherited as mendelian traits and might associate with a trait such as susceptibility to disease. [Pg.1576]


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See also in sourсe #XX -- [ Pg.16 ]




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Associated pair

Base pairing bases

Base pairs

Bases Base pair

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