Amino Acids Flashcards

1
Q

What are amino acids and how do they build polypeptide chains?

A

Amino acids are monomers or proteins. Amino acids are joined by peptide bonds during condensation reactions to form polypeptide chains.

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2
Q

What is common structure of amino acids?

A
  • Carboxylic acid -COOH
  • Amino group - NH2
  • H atom
  • R group (unique for every amino acid so determines identity)
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3
Q

Polypeptide chain has directionality. What does this mean?

A

Two ends of chain are chemically distinct. N-terminus (amino end) has a free amino group. C-terminus (carboxyl end) has a free carboxyl group.

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4
Q

What determines chemical behaviour of amino acid?

A

The R group

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5
Q

Lysine (at physiological pH)

A

Electrically charged: side chain is positively charged. Considered basic amino acid

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6
Q

Acidic Amino Acids: side chains are negatively charged

A
Aspartic acid (Asp)
Glutamic acid (Glu)
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7
Q

Basic Amino Acids: side chains are positively charged

A

Lysine (Lys)
Arginine (Arg)
Histidine (His)

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8
Q

Non-Polar (Hydrophobic) Amino Acids

A
Glycine (Gly) 
Alanine (Ala)
Valine (Val) 
Leucine (Leu) 
Isoleucine (Ile)
Methionine (Met)
Tryptophan (Trp) 
Phenylalanine (Phe)
Proline (Pro)
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9
Q

Polar (Hydrophilic) Amino Acids

A
Serine (Ser)
Threonine (The)
Cysteine (Lys)
Tyrosine (Tyr)
Asparagine (Asn)
Glutamine (Gln)
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10
Q

Glycine at physiological pH?

A

Non-polar (hydrophobic)

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11
Q

Histidine at physiological pH?

A

Side chain is positively charged: basic amino acid.

ALTHOUGH, at pH 7 side chain is mainly uncharged

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12
Q

Arginine at physiological pH?

A

Side chain is positively charged: basic amino acid

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13
Q

Which is the only amino acid that isn’t chiral / doesn’t posses optical activity?

A

Glycine

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14
Q

What do optical isomers do?

A

Rotate plane-polarised light in opposite directions

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15
Q

What is physiological pH?

A

7.2-7.4

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16
Q

At physiological pH, what is the amino group and carboxyl group typically like?

A

Amino group typically protonated (has positive charge)

Carboxyl group typically deprotonated (has negative charge)

17
Q

What is pKa?

A

The pH at which a group is 50% ionised

18
Q

What is the pKa for carboxylic acid groups?

A

Roughly 1.8 – 2.5; almost always negatively charged

19
Q

What is the pKa for amino groups?

A

Roughly 9-10; almost always positively charged

20
Q

What is the pKa for histidine?

A

Roughly 6.0

21
Q

If a pH is below pKa, what is seen?

A

Group will have H attached