Chapter 3 Flashcards

1
Q

All amino acids have a chiral carbon and are stereoisomers except:

A

glycine

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

Although amino acids are stereoisomers, only…

A

L stereoisomers are found in proteins

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

all amino acids have:

A
  • carboxyl group
  • amino group
  • alpha carbon
  • R group (side chain)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Which amino acid is often found at turns of polypeptides?

A

proline, in combination with glycine

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

Which two amino acids have a sulphur group within its side chain?

A

Methionine and Cysteine

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

The non-polar amino acids are…

A

hydrophobic and buries in the core of a protein

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

Aromatics have…

A

ring groups

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

Biggest amino acid

A

Tryptophan

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

Smallest amino acid

A

glycine

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

Phosphorylation

A

introduces a phosphate group to a compound; central mechanism to regulate protein function

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

Post Translational Modification

A
  • an often reversible modification where phosphoric groups are added by kinases to specific hydroxyl-group containing amino acids
  • changes property –> activity
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

How can post translational modification be reversed?

A

adding phosphatases (removes phosphate group)

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

What amino acids can undergo phosphorylation?

A

Tyrosine
Serine
Threonine

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

How are disulfide bonds formed?

A

form through the oxidation of sulfhydryl groups of two Cysteine residues (covalent linkage)

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

What do disulfude bonds do?

A

help stabilize the structures of protein

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

Which amino acids ALWAYS have a positive charge?

A

Lysine and Arginine

17
Q

Which amino acid has a potential to carry a positive charge?

18
Q

Glutamate is responsible for….

A

umami taste

19
Q

Aspartate and Glutamate have….. in their side chains

A

carboxyl groups

20
Q

amphoteric

A

can act as both weak acids and bases (amino acids for ex.)

21
Q

zwitterion

A

one group has a positive charge, one groups has a negative

22
Q

diprotic

A
  • has 2 groups that accept and donate protons (carboxyl and amino groups)
  • 2 buffering regions
23
Q

triprotic

A

3 buffering regions

24
Q

triprotic amino acids

A
  • have ionizable groups

- Lys, Arg, His, Asp, Glu, Cys, Tyr

25
at pKa...
there is equal numbers of protonated and unprotonated forms (where that groups changes protonation state)
26
pH below pKa
protonated form dominates (HA, weak acid)
27
pH above the pKa
unprotonated form dominates (A-, conjugate base)
28
isoelectric point (pI)
the average of the pKa's on either side where the net charge is zero
29
pI equation
pI = (pKa1 + pKa2)/2
30
Diprotic amino acids all have similar....
titration curves and isoelectric points
31
peptide bond
covalently links amino acids
32
How do peptide bonds form
by condensation/dehydration reactions (loss of water molecule) between carboxyl of one amino acid and the amino group of another.
33
How to break peptide bonds
just add water!!
34
Map this shit
amino acids ---> peptide chains --->proteins
35
N-terminus
amino
36
C-terminus
carboxyl
37
What direction do you read amino acid chain sequences?
N-terminus to C-terminus
38
Which functional groups have a charge?
- carboxyl - phosphoryl - phosphoanhydride
39
Which functional groups have 2 R groups?
- carbonyl (ketone) | - disulfide