Chapter 2 & 4 - Nucleic Acids Flashcards
How many nucleotides is one DNA turn made up of?
10.5
How wide is the minor groove?
12 Å or 1.2 nm
How wide is the major groove?
22 Å or 2.2 nm
How wide is a double helix?
20 Å
What is the centre-to-center distance between adjacent nucleotide pairs?
3.4 Å
At which carbon on the sugar is the H attached to in deoxyribose?
At carbon 2.
Which carbon carries the nitrogen base with a glycosidic bond?
Carbon number 1.
Which are carbons are the reactive moieties on deoxyribose?
The 3’ OH is the reactive moiety for formation of phopshopdiesterbonds. The 5’ OH is another reactive moiety.
How does phophodiester bond formation occur?
When adding nucleotides to the 3′ end of a polynucleotide chain the polymerase catalyzes the nucleophilic attack of the 3′-hydroxyl group terminus of the polynucleotide chain on the α-phosphate group of the nucleoside triphosphate that is added. For the initiation of this reaction, DNA polymerases require a primer with a free 3′-hydroxyl group already base-paired to the template and cannot start from scratch by adding nucleotides to a free single-stranded DNA template.
(Adenine-deoxyribose-triphosphate –> triphosphate attached to the 5’ carbon. Phosphates are connected by high energy bonds. The 3’ OH groups acts as the nucleophile ad donates a pair of electrons to the phosphate.)
How does Glycosidic bond/linkage occur?
OH group the 1’carbon reacts with the H (N9) of the nitrogenous base and releasing a water molecule.
At which positions on the bases do hydrogen bond formation occur?
A:T
Adenine and thymine match up so that a hydrogen bond can form between the exocyclic amino group at C6 and adenine at the carbonyl at C4 in thymine.Hydrogen bond can form between N1 of adenine and N3 of thymine.
G:C
NH2 at C2 on guanine hydrogen-bonds with a carbonyl at C2 on cytosine. N1 of guanine and N3 of cytosine form a bond. And the carbonyl at C6 of guanine can form a hydrogen bond with the NH2 at C4 of cytosine.
What is an amino acid?
Imino acid = contains both an imine (C=NH) and a carboxyl group.
Explain base stacking.
Induces by dipole-dipole and partial charge interaction between rings of the bases. (G:C have stronger stacking interactions)
How are the 3’ and 5’ ends chemically different?
The 3’ end carries an unlike -OH group attached to the 3’ position on the sugar ring; the 5’ carries a free phosphate group attached to the 5’ position on the sugar ring.
How does the chemical information differ between the major and minor groove?
Major groove ADHM
Minor groove ADA/AHA (symmetrical)