Chapter 3 Flashcards
All amino acids have a chiral carbon and are stereoisomers except:
glycine
Although amino acids are stereoisomers, only…
L stereoisomers are found in proteins
all amino acids have:
- carboxyl group
- amino group
- alpha carbon
- R group (side chain)
Which amino acid is often found at turns of polypeptides?
proline, in combination with glycine
Which two amino acids have a sulphur group within its side chain?
Methionine and Cysteine
The non-polar amino acids are…
hydrophobic and buries in the core of a protein
Aromatics have…
ring groups
Biggest amino acid
Tryptophan
Smallest amino acid
glycine
Phosphorylation
introduces a phosphate group to a compound; central mechanism to regulate protein function
Post Translational Modification
- an often reversible modification where phosphoric groups are added by kinases to specific hydroxyl-group containing amino acids
- changes property –> activity
How can post translational modification be reversed?
adding phosphatases (removes phosphate group)
What amino acids can undergo phosphorylation?
Tyrosine
Serine
Threonine
How are disulfide bonds formed?
form through the oxidation of sulfhydryl groups of two Cysteine residues (covalent linkage)
What do disulfude bonds do?
help stabilize the structures of protein
Which amino acids ALWAYS have a positive charge?
Lysine and Arginine
Which amino acid has a potential to carry a positive charge?
Histidine
Glutamate is responsible for….
umami taste
Aspartate and Glutamate have….. in their side chains
carboxyl groups
amphoteric
can act as both weak acids and bases (amino acids for ex.)
zwitterion
one group has a positive charge, one groups has a negative
diprotic
- has 2 groups that accept and donate protons (carboxyl and amino groups)
- 2 buffering regions
triprotic
3 buffering regions
triprotic amino acids
- have ionizable groups
- Lys, Arg, His, Asp, Glu, Cys, Tyr
at pKa…
there is equal numbers of protonated and unprotonated forms (where that groups changes protonation state)
pH below pKa
protonated form dominates (HA, weak acid)
pH above the pKa
unprotonated form dominates (A-, conjugate base)
isoelectric point (pI)
the average of the pKa’s on either side where the net charge is zero
pI equation
pI = (pKa1 + pKa2)/2
Diprotic amino acids all have similar….
titration curves and isoelectric points
peptide bond
covalently links amino acids
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.
How to break peptide bonds
just add water!!
Map this shit
amino acids —> peptide chains —>proteins
N-terminus
amino
C-terminus
carboxyl
What direction do you read amino acid chain sequences?
N-terminus to C-terminus
Which functional groups have a charge?
- carboxyl
- phosphoryl
- phosphoanhydride
Which functional groups have 2 R groups?
- carbonyl (ketone)
- disulfide