Lecture 5 Flashcards
7 functions of nucleotides and nucleic acids
Energy for metabolism (ATP), enzyme cofactor (NAD+), signal transduction (cAMP), storage of genetic info (DNA), transmission of genetic info (mRNA), catalysis (ribozymes), and protein synthesis (tRNA and rRNA).
Nucleotide composition
nitrogenous base, pentose, and phosphate moiety
Nucleoside composition
nitrogenous base and pentose
DNA runs in which direction
5’ to 3’
Ribose vs deoxyribose position
Ribose: OH in 2’ carbon
Deoxyribose: H in 2’ carbon
Phosphate moiety is attached to which carbon
5’ Carbon
Where does the nitrogenous base attach?
1’ carbon
Another name for the 1’ Carbon on a pentose
anomeric carbon
Beta designation
5’ moiety and 1’ base are in the same plane, either both above or both below
Alpha designation
5’ moiety and 1’ base are in opposite planes
NMP
Nucleo monophosphate
NDP
Nucleo diphosphate
NTP
Nucleo triphosphate
D designation
If the OH goes to the right on the most distal carbon in a fischer projection
L designation
If the OH goes to the left on the most distal carbon in a fischer projection
Fischer projection bond directions - horizontal vs vertical
horizontal - coming out of the page
vertical - going into the page
Heteroaromatic molecules
multiple different bases are present in the composition of the ring structure
Nucleobases UV light absorption
250-270 nm
Pyrimidine bases
Cytosine (DNA), Thymine (DNA), and Uracil (RNA)
Purine bases
Adenine and guanine
Type of bond formed between the nitrogenous base and the anomeric carbon
N-glycosidic bond
Bond formed position in pyrimidines
N1
Bond formed position in purines
N9