CBS - Amino Acids Flashcards

- recognise the structures of the 20 common amino acids - identify the functional importance of amino acid side chains

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1
Q

Describe what an amino acid is.

A

It is a molecule with an amino group and carboxylic group attached to the same carbon (known as the α- carbon).

Amino acids have different R-groups attached to the α- carbon. The R-group defines the physical properties and function of the amino acid.

The amino and carboxyl group are ionised at physiological pH.

There are 20 universal DNA-encoded amino acids that exist.

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2
Q

Define essential amino acids (in adults).

A

They are amino acids that cannot be synthesised de novo by humans, as we lack the necessary enzymes.

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3
Q

List the essential amino acids.

A
  • threonine
  • methionine
  • lysine
  • valine
  • leucine
  • isoleucine
  • histidine
  • phenylalanine
  • tryptophan
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4
Q

List the two negatively charged amino acids.

A

Aspartic acid (Asp)

Glutamic acid (Glu)

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5
Q

List the three positively charged amino acids.

A

Arginine (Arg)

Lysine (Lys)

Histidine (His) (sometimes)

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6
Q

Why is histidine important?

A

It has a complex nitrogen carbon ring structure, and because of the pKa of this amino acid, it can be positively charged or not.

Hence, it plays an important part in buffering haemoglobin but also other proteins.

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7
Q

List the uncharged, polar/hydrophilic amino acids, with an amide R group.

A

Asparagine (Asn)

Glutamine (Gln)

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8
Q

List the uncharged polar/hydrophilic amino acids, with a hydroxyl R group.

A

Serine (Ser)

Threonine (Thr)

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9
Q

List the uncharged polar/hydrophilic amino acid, with a benzene ring R group.

A

Tyrosine (Tyr)

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10
Q

List the nonpolar amino acid, with no R group.

A

Glycine (Gly)

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11
Q

List the nonpolar/hydrophobic amino acids, with an aliphatic R group.

A

Alanine (Ala)

Valine (Val)

Leucine (Leu)

Isoleucine (Ile)

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12
Q

List the nonpolar/hydrophobic amino acid, with a ring structure (including an α-amino R group).

A

Proline (Pro)

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13
Q

List the nonpolar/hydrophobic amino acid, with a benzene ring R group.

A

Phenylalanine (Phe)

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14
Q

List the nonpolar/hydrophobic amino acid, with a sulphur-containing R group.

A

Methionine (Met)

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15
Q

List the nonpolar/hydrophobic amino acid, with a ring structure R group.

A

Tryptophan (Trp)

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16
Q

List the nonpolar/hydrophobic amino acid, with a ring structure R group.

A

Cysteine (Cys)

17
Q

List some examples of clinical considerations of amino acid changes.

A

PHENYLKETONURIA (PKU):
This results in a defective phenylalanine hydroxylase (which converts phe→tyr)

The reduced tyrosine results in reduced dopamine production, as well as reduced melanin production.

There is also an increase in other phenylalanine by-products e.g. phenylacetate

ALBINISM (many forms):
This comes as a reults of a defective tyrosinase (which converts tyr → melanin)