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Abundances are given as pollution free monthly mean mole fractions in parts-per-trillion. Atmospheric concentration of CF 4 (PFC-14) vs. similar man-made gases (right graph). Note the log scale. Tetrafluoromethane is a potent greenhouse gas that contributes to the greenhouse effect.
Four-carbon molecules are based on a skeleton made from four carbon atoms. They may be in a chain, branched chains, cycles or even bicyclic compounds C 4 H 4 isomers with CAS registry numbers
Secondary structure is the set of interactions between bases, i.e., which parts of strands are bound to each other. In DNA double helix, the two strands of DNA are held together by hydrogen bonds. The nucleotides on one strand base pairs with the nucleotide on the other strand. The secondary structure is responsible for the shape that the ...
The chemical structure of DNA is insufficient to understand the complexity of the 3D structures of DNA. In contrast, animated molecular models allow one to visually explore the three-dimensional (3D) structure of DNA. The DNA model shown (far right) is a space-filling, or CPK, model of the DNA double helix. Animated molecular models, such as ...
The two pathways for homologous recombination in eukaryotes, showing the formation and resolution of Holliday junctions. The Holliday junction is a key intermediate in homologous recombination, a biological process that increases genetic diversity by shifting genes between two chromosomes, as well as site-specific recombination events involving integrases.
Chemical structure of DNA; hydrogen bonds shown as dotted lines. Each end of the double helix has an exposed 5' phosphate on one strand and an exposed 3′ hydroxyl group (—OH) on the other. DNA is a long polymer made from repeating units called nucleotides.
Chemical structure of DNA, showing four nucleobase pairs produced by eight nucleotides: adenine (A) is joined to thymine (T), and guanine (G) is joined to cytosine (C). + This structure also shows the directionality of each of the two phosphate-deoxyribose backbones, or strands.
The wide range is due to the sensitivity of the stretching frequency to other substituents in the molecule. Monofluorinated compounds have a strong band between 1000 and 1110 cm −1; with more than one fluorine atoms, the band splits into two bands, one for the symmetric mode and one for the asymmetric. [13]