Week 26 / Amino Acids Flashcards

1
Q

Q: What are proteins and many other important biomolecules made from?

A

A: Amino acids.

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2
Q

Q: What are the amino acids most commonly found in nature called?

A

A: α-amino acids (alpha-amino acids).

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3
Q

Q: Which amino acid is the only achiral member of the 20 common amino acids?

why?

A

A: Glycine.
This is because glycine has a hydrogen atom as its side chain

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4
Q

Q: In which optical form do the 19 chiral amino acids most commonly exist?

A

A: The L-optical form.

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5
Q

Q: Why are amino acids considered amphoteric molecules?

A

A: Because they contain both an acidic group (carboxyl group, -COOH) and a basic group (amino group, -NH2).

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6
Q

Q: What does the term “amphoteric” mean in relation to amino acids?

A

A: It means they can act as both an acid (donating a proton) and a base (accepting a proton).

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7
Q

Q: Which amino acids have nonpolar, aliphatic R groups?

A

A: Glycine, Alanine, Proline, Valine, Leucine, Isoleucine, and Methionine.

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8
Q

Q: Which amino acids have polar, uncharged R groups?
[STAGC]

A

A: Serine, Threonine, Cysteine, Asparagine, and Glutamine.

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9
Q

Q: Which amino acids have aromatic R groups?
[TPT]

A

A: Phenylalanine, Tyrosine, and Tryptophan.

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10
Q

Q: What property of peptide bonds provides them with significant stability?

A

A: Peptide bonds exhibit strong resonance, resulting in delocalization of electrons between the carbonyl oxygen and the amide nitrogen.

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11
Q

Q: How much does resonance energy stabilize peptide bonds?

A

A: The delocalization energy stabilizes peptide bonds by 75-90 kJ/mol.

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12
Q

Q: Why do peptides prefer a planar conformation?

A

A: The resonance in peptide bonds gives them partial double-bond character, restricting rotation and favoring a planar, trans (anti/Z) conformation.

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13
Q

Q: Where does the naming of a peptide or protein start?

A

A: At the N-terminal amino acid (the amino acid with a free amino group, -NH2).

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14
Q

Q: How many chains of amino acids make up insulin?

A

A: Two chains of amino acids.

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15
Q

Q: How are the two chains of insulin linked?

A

A: By disulfide bonds.

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16
Q

Q: How many commonly occurring amino acids are there?

17
Q

Q: What type of bond links amino acids together?

A

A: Peptide bonds, forming amides.

18
Q

Q: What do we call longer chains of amino acids?

A

A: Polypeptides, and the largest chains are proteins.

18
Q

Q: What are short chains of amino acids called?

A

A: Oligopeptides.

19
Q

Q: When naming sequences of amino acids, where do we start?

A

A: From the amino terminus (N-terminus).

20
Q

Q: Besides peptide bonds, how else can amino acids be linked?

A

A: Via disulfide bonds.

21
Q

Whats a dipeptide ?
Whats a Oligopeptides?

A

a protein that contains two amino acids

a protein contain 2-10 amino acids

22
Q

Whats the only amino acid linked by disulphide bond?

23
Q

What does Glutathione form?

What are they linked by?

A

Forms disulphide in presence of oxidizing agents.

via sidechain Glu acid