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nucleotide structure
Nitrogenous base pyrimidine (C, U, T) vs purine (A, G)
Pentose sugar (ribose, deoxyribose)
1-3 phosphate group(s)
Deoxyribonucleic Acid(DNA)
Pentose sugar: deoxyribose(just H on carbon 2')
Nitrogenous bases: adenine, guanine, cytosine, thymine
Antiparallel
Bonds: phosphodiester, hydrogen, hydrophobic effects, and van der waals forces
Ribonucleic Acid(RNA)
Pentose sugar: ribose(OH on carbon 2')
Nitrogenous bases: adenine, guanine, cytosine, uracil
Antiparallel if in 2 strand form
Bonds: phosphodiester, hydrogen, hydrophobic effects, and van der waals forces
Pyrimidines
cytosine, thymine, uracil (1 ring-6 membered)
Purines
guanine, adenine (2 ring-6 membered+5 membered)
Deoxyribose
5-carbon sugar, has H on 2'
Ribose
5-carbon sugar, has OH on 2'
Phosphodiester bonds
Bonds between phosphate group and pentose sugar in nucleic acids. using 2 ester bonds
1st ester bond
OH on phosphate group + OH C 3' -> H2O + combined suagr and phosphate group w/ only O remaining
2nd ester bond
OH on phosphate group + OH C 5' -> H2O + combined suagr and phosphate group w/ only O remaining
sugar-phosphate backbone
The alternating chain of sugar and phosphate to which the DNA and RNA nitrogenous bases are attached
Nucleoside
base + sugar