202 MT 1 Flashcards

1
Q

Properties of water? Why is it a good solvent for polar or charged molecules?

A

Bent shape making it polar and able to form multiple hydrogen bonds.

Cohesive - Water molecules bonding with each other.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

How does water affect electrostatic interactions?

A

Water molecules compete for their charge reducing electrostatic interactions by 80x.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

First and second laws of thermodynamics

A

Energy can not be created or destroyed only modified.

The total entropy of a system always increases for a spontaneous process.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

How can entropy decrease locally?

A

Entropy can be decreased locally in the formation of ordered structures only if the entropy of the universe is increased by an equal or greater amount.

I.e. Heat being released

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Enthalpy

A

H, Heat content of the system.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Gibbs Free energy equation and spontaneity

A

ΔG = ΔH - T ΔS

0 > ΔG = Spontaneous

If ΔH < 0 (releasing heat) ΔG becomes more spontaneous

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Cage effect

A

Non-polar molecules tend to cluster together.

Water molecules form a cage around the hydrophobic molecules.

Fewer water molecules are needed to form one big cage as opposed to multiple small cages.

Increases entropy.q

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Buffers

A

Mixture of weak acid and conj base. Resists change sin pH because both forms are present and able to donate/accept protons.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What are the charges of carboxy and amide groups between
2-9 pH?

A

Zwitter ions - COO- and NH3+

Positive and negative charge.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Peptide bond

A

Linkage of an alpha-carboxyl linked to the amino group of another amino acid. h20 byproduct.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Where would you find the amino-terminal end versus the free carboxyl group?

A

Amino-terminal end (N) is on the left

Free carboxyl group on the right (C)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What would K 614 P denote?

A

The 614th residue from the N termincal end would change from Lysine to Proline.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Phi vs Psi angle

A

Phi angle is the rotation about the Alpha carbon - nitrogen bond.

Psi angle is the rotation about the alpha carbon - carbonyl.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Why is there no rotation about the peptide bond?

A

Peptide bond has double bonding characteristics due to resonance between peptide bond and carbonyl.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What produces flexibility, allowing the backbone to fold?

A

The bonds between αC-N and αC-Carboxyl are free to rotate.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Length added per residue for parallel, anti-parallel and α-helix?

A

Parallel 3.25 and anti-parallel = 3.5

A-helix = 1.5

17
Q

Parallel B-Strand bonding

A

N-H of residue i bonds with j carbonyl and carbonyl of i bonds with N-H of j+2.

Has to “reach over”