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15 Cards in this Set

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  • 3rd side (hint)
Name the Purines, their functional groups and number of carbons
Adenine and Guanine,
NH2
O= and NH2,
9
PAG9
Name the Pyrimidines, their functional groups, and number of carbons
Cytosine, Uracil, Thymine,
O= NH2,
O= O=,
O=,O= CH3,

6
Pyrcut 6
IOU (uracil with 2 O=)
Molecular Properties of Purines and Pyrimidines (there are 6)
Weak Bases, Flat/Planar, Absorb UV light, Hydrophobic at neutral pH, Base stacking via van der Waals, H bonding between base pairs
think about placement/function in DNA
Describe Nucleoside structure
Purine/Pyrimidine+Sugar (ribose or 2' deoxyribose)
N-Glycosidic Bond is between ____ and _____

Which conformation is at always in?
Base and Ribose, Anti position (Beta configuration)
Describe Nucleotide structure
Nucleoside+Phosphate Ester
What are the names of the different phosphate groups/what kind of bonds connect them?
Alpha, Beta, Gamma,

Phophoester bonds connects to ribose

Phosphoanhydride bond connect btw phosphates
AMP stands for?
Adenosine Monophosphate
Thymidylate is always ?
always deoxy
UMP?
Uridylate
Hydrolysis of what kind of bonds provides energy for cellular rxns?
Phosphoester/phophoanhydride
name all 4 energy carriers. what is the most common?
GTP, CTP, UTP, ATP most common
Adenosine is a structural component of what? give 2 examples
coenzymes,
NAD+ and FAD
G-Proteins are involved in?
Signal transduction
Name 2 types of signal transducers and their precursors
cAMP and cGMP and made from ATP and GTP via cyclase enzymes