Term
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Definition
~ Building Blocks of Proteins
~a central C atom with substituents (NH3+, COOH-, H) and the R group that gives it its name
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Term
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Definition
Molecule bearing groups with opposite charge. Ex: COO- will be protonated; NH3+ will be deprotonated |
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Term
Stereochemistry... All amino acids in proteins exist as the ___ isomer. They are: chiral or achiral? |
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Definition
All amino acids in proteins exist as the L isomer. They are chiral, meaning nonsuper-imposable. |
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Term
Nonpolar Aliphatic Side Chains? |
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Definition
Glycine (is the only one not chiral), Alanine, Proline (contains N), Valine, Leucine, Isoleucine, Methionine (contains S) |
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Term
Aromatic Side Chain groups |
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Definition
Phenylaline (most hydrophobic), Tyrosine (contains -OH/phenol), Tryptophan (contains multiple rings) |
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Term
Polar, Uncharged Side chains |
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Definition
Serine, Threonine, Cysteine (contains S). Also, Asparagine & Glutamine, which both contain an amide R-group. *ALL act as e- donors/acceptors |
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Term
Disulfide Bonds are formed by: |
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Definition
Cysteine. This is in reduced and oxidized formations. |
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Term
Acidic (- charged) Side Chains |
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Definition
Aspartate & Glutamate (contains 1 extra carbon) In solid state, is acidic, once dissolved, proton falls off, therefore (-) charged. |
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Term
Basic (+ charged) Side Chains |
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Definition
Lysine (large 4C chain with amine that's protonated), Arginine (has C=NH2), & Histidine |
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Term
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Definition
pH where there is no net charge |
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Term
_________ contains a side chain most likely to be found in the interior of a protein? |
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Definition
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Term
___________ has a side chain that is mostly charged at pH = 8 |
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Definition
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Term
___________ has a side chain that contains a nitrogen atom. |
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Definition
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Term
This amino acid contains an –R group that is a hydrogen bond acceptor at pH 8. |
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Definition
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Term
For lysine, pK1=2.18, pK2=8.95, pK3=10.53
What is the pI? |
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Definition
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Term
What amino acid is not commonly found in the hydrophobic core of a protein domain? |
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Definition
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Term
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Definition
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Term
Shown below is the titration curve for a different amino acid. The pKa of the side chain (i.e. the R group) of this amino acid is approximately ____
[image] |
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Definition
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Term
Given the following titration curve of Arg, the pI of Arg is approximately (use the pKas, etc. of this titration curve):
[image] |
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Definition
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Term
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Definition
Alanine
Ala
A
nonpolar
side chain charge: neutral |
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Term
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Definition
Arginine
Arg
R
polar
side chain charge: + |
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Term
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Definition
Asparagine
Asn
N
polar
Side chain charge: neutral |
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Term
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Definition
Aspartic Acid
Asp
D
polar
Side chain charge: - |
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Term
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Definition
Cysteine
Cys
C
nonpolar
Side chain charge: neutral |
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Term
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Definition
Glutamic Acid
Glu
E
polar
Side chain charge: - |
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Term
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Definition
Glutamine
Gln
Q
polar
Side chain charge: neutral |
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Term
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Definition
Glycine
Gly
G
nonpolar
side chain charge: neutral |
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Term
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Definition
Histidine
His
H
polar
Side chain charge: mostly neutral, slightly + |
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Term
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Definition
Isoleucine
Ile
I
nonpolar
side chain charge: neutral |
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Term
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Definition
Leucine
Leu
L
nonpolar
side chain charge: neutral |
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Term
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Definition
Lysine
Lys
K
polar
side chain charge: + |
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Term
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Definition
Methionine
Met
M
nonpolar
neutral side chain |
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Term
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Definition
Phenylalanine
Phe
F
nonpolar
neutral side chain |
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Term
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Definition
Serine
Ser
S
polar
neutral side chain |
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Term
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Definition
Threonine
Thr
T
polar
neutral side chain |
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Term
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Definition
Tryptophan
Trp
W
nonpolar
neutral side chain |
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Term
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Definition
Tyrosine
Tyr
Y
polar
neutral side chain |
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Term
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Definition
Valine
Val
V
nonpolar
neutral side chain |
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Term
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Definition
Proline
Pro
P
nonpolar
neutral side chain |
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