Amino Acids Flashcards

1
Q

How many amino acids are there?

A

20

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2
Q

Peptide bond

A

A bond between an amino group ( n terminus) and a carboxyl group ( c terminus)

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3
Q

Disulphide bond

A

A bond between sulphur groups that is usually formed following an oxidation reaction.

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4
Q

G(gln)

A

Glutamine

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5
Q

G(gly)

A

Glycine

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6
Q

V(Val)

A

Valine

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7
Q

Phosphomimetic

A

Amino acids that mimic phosphorylated amino acids when activated. This is seen in glutamate and aspartate, the activated forms of glutamine and asparagine respectively.

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8
Q

Chiral

A

When there are 4 different structures bound to an alpha protein.

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9
Q

Non-polar amino acids

A

Any amino acid that has an overall equal charge

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10
Q

Which types of amino acids can undergo phosphorylation

A

Amino acids with and OH group in their side chain

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11
Q

Side chain

A

Makes the amino acid unique and determines the property of the amino acids.

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12
Q

List 5 types of amino acids

A
Aromatic
Neutral
Acidic 
Basic
Alkyl
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13
Q

T/F

All amino acids have a carboxyl group

A

True

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14
Q

C(cys)

A

Cysteine

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15
Q

H(his)

A

Histidine

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16
Q

N(asn)

A

Asparagine

17
Q

M(met)

A

Methionine

18
Q

W(trp)

A

Tryptophan

19
Q

T/F

All amino acids are hydrophobic

A

False.
Only non-polar amino acids are hydrophobic. Polar amino acids like to interact with other polar molecules and are therefore hydrophilic.

20
Q

T/F

Histidine has an overall positive charge

A

False

Histidine is a base, but it is an exception to the rule as it has neutral charges.

21
Q

Anion

A

Negatively charged atom

22
Q

Cation

A

Positively charged atom

23
Q

Phosphatase

A

A component involved in dephosphorylation

24
Q

T/F

Carboxylic acids are hydrogen accepting

A

False

Carboxylic acids are hydrogen donating, while nitrogens are hydrogen accepting.

25
Q

L/D amino acid

A

Shows the side on the Fisher projection where the amino group is located. E.g L amino acid means there is an amino group on the left side of the amino group.

26
Q

Why are di-sulphide bonds relevant in proteins?

A

Disulphide bonds are important for the strength and integrity of proteins and this process is commonly seen with tertiary and quaternary proteins. One such example is the transition from cysteine to cystine, which requires the removal of a hydrogen atom in exchange for a bond. This explains the rigidity in human hair.

27
Q

T(thr)

A

Threonine

28
Q

E(glu)

A

Glutamate

29
Q

D(asp)

A

Aspartate

30
Q

K(Lys)

A

Lysine

31
Q

S(ser)

A

Serine

32
Q

P(pro)

A

Proline

33
Q

I(ile)

A

Isoleucine

34
Q

A(alu)

A

Alanine

35
Q

F(phe)

A

Phenylalanine

36
Q

R(arg)

A

Arginine

37
Q

L(leu)

A

Leucine