Transition from right-handed to left-handed DNA
β Scribed by Gaspar Banfalvi
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- English
- Weight
- 304 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0307-4412
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π SIMILAR VOLUMES
Many natural shapes are chiral (or handed). Our hands, for example, have a right-hand version and a left-hand version, the two types being mirror images of each other. Molecules are also classified according to their chirality, which determines their chemical characteristics. Glucose, for example, i
Using the semiempirical potential functions, conformational energies of the model compounds DMP-, d(pCp), d(pGp), and d(pCpGpCp) are calculated, and the B -Z transition is discussed along the pseudorotational path of the sugar ring. For dimethylmonophosphate anion, DMP-, the energy contour map is pr
Molecular mechanical simulations on base-paired deoxyhexanucleoside phosphates, (dAdT), . (dAdT),, (dTdA), . (dTdA),, (dGdC), . (dGdC),, and (dCdG), . (dCdG),, have been carried out to assess their energetic stabilities in left-and right-handed forms. These hexamers have also been simulated with al
Bovine zeta-crystallin has the ability to bind with different DNAs. Initially, this protein was named regulatory factor 36 (Kang et al., 1985), but it has been shown to be an ocular lens zeta-crystallin (JΓΆrnvall et al., 1993), which is considered an enzyme-crystallin (Rodakanaki et al., 1989). The