Biochem- Amino Acids and Residues Flashcards

1
Q

Which Amino Acids are Non-Polar, Non-Aromatic?

A

Glycine, Alanine, Valine, Leucine, Isoleucine , Methionine, Proline
(GAVLIMP)

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2
Q

Which Amino Acids are Non-Polar, Aromatic?

A

Tryptophan, Phenylalanine, Tyrosine
(WFY)
( Tyrosine= polar, Tryptophan and Phenylalanine= Non-polar)

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3
Q

Which Amino Acids are Polar ?

A

Serine, Threonine, Asparagine, Glutamine, Cysteine

S,T,N,Q,C

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4
Q

Negative Charged Side chains ( acidic )

A

Aspartate (aspartic acid), Glutamate ( glutamic acid)

D,E) ( DEA - acidic

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5
Q

Positive Charged Side chains (basic)

A

Arginine, Lysine, Histidine

KRH

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6
Q

Glycine side chain and abbreviations (1, 3)

A

2 H’s on Side chain position, Gly, G

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7
Q

Alanine side chain and abbreviations

A

CH3 group , Ala , A

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8
Q

Valine side chain and abbreviations

A

Isopropyl group ( CH, CH3x2), Val, V

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9
Q

Where do the side chains come off of ?

A

the central carbon, between the amine and carboxyl group

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10
Q

Leucine side chain and abbreviations

A

isobutyl side chain ( CH,CH2, CH3x2), Leu, L

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11
Q

Isoleucine side chain and abbreviations

A

isomer of leucine, intead of isobutyl- has sec-butyl side chain, Ile, I

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12
Q

Methionine side chain and abbreviations

A

2 Ch2- Sulfur- CH3, Met, M

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13
Q

Proline side chain and abbreviations

A

3 C chain that loops around and connects back to parent amino, Pro, P

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14
Q

Tryptophan side chain and abbreviations

A

only AA with 2 fused rings, one contains another Nitrogen group, Trp , W

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15
Q

Phenylalanine side chain and abbreviations

A

1 attached benzene ring, Phe, F

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16
Q

Tyrosine side chain and abbreviations, Polarity/ Hydrophobicity note

A
Benzyl group ( benzene ring with OH), Tyr, Y
Relatively Polar, But still Hydrophobic
17
Q

Serine side chain and abbreviations

A

CH2- OH, Ser, S

18
Q

Threonine side chain and abbreviations

A

3 different groups- CH, CH3, OH, Thr , T

19
Q

Asparagine side chain and abbreviations

A

Amide ( CH2-C=O- NH2), Asn, N

20
Q

Glutamine side chain and abbreviations

A

extra CH2 from asparagine , Amide ( CH2x2- C=O-NH2), Gln, Q

21
Q

Cysteine side chain and abbreviations, polarity/ hydrophobicity

A

contains only thiol group ( CH2-SH), Cys, C, slightly polar but still hydrophobic

22
Q

Aspartate side chain and abbreviations, and protonated form

A

CH2-C=O-O^-1, (anion form), Asp, D

protonated form: CH2-C=O-OH ->aspartic acid

23
Q

glutamate side chain and abbreviations, and protonated form

A

CH2-CH2-C=O-O^-1 ( anion form), Glu, E

protonated form: CH2-CH2- C=O- OH -> glutamic acid

24
Q

Arginine side chain and abbreviations

A

long nitrogen filled sidechain with a double bonded N (CH2x3- NH-C=NH- H2N), Arg, R

25
Lysine side chain and abbreviations
long C chain (CH2x4), ending with H2N, Lys, K
26
Histidine side chain and abbreviations
imidazole side chain ( heterocyclic, with an N=C and an N-H group within the ring), His , H
27
are the + charged side chains acidic or basic?
basic
28
are the - charged side chains acidic or basic ?
acidic
29
At low pH, what protonated form do the amino acids exist in ( + vs - charge)? How do acidic amino acids behave?
fully protonated ( +charge), acidic AA's have a pI well below 6
30
At high pH, what protonated form do the amino acids exist in ( + vs - charge)? How do basic amino acids behave?
fully deprotonated ( - charge), basic AA's have a pI well above 6
31
At pH near pI, what form does the amino acid exist in and how do uncharged amino acids behave?
AA is neutral= zwitterion, AA with no charge have a pI around 6
32
What is an amino acids pI? How does it affect AA solubility?
Isoelectric point, point at which the molecule is neutral, Amino acids are least soluble at pI
33
General formula for pI
pI= (pKa1 + pKa2)/2
34
What amino acid is the only non-chiral AA?
glycine
35
What is the stereochemsitry and chirality of most amino acids?
L chirality, S stereoisomer configuration
36
which amino acid doesn't have the usual stereochemistry?
cysteine: L-chirality , R configuration