Amino Acids - w1 Flashcards

1
Q

What are the two main molecular groups in an amino acid?

A

carboxyl group (COO-) and amino group (H3N+)

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2
Q

What type of peptide chains are short (<20 AAs)

A

oligopeptide

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3
Q

What is the bond between amino acids?

A

peptide bond

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4
Q

What are zwitterions?

A

ions that have a positively charged area on one end and a negatively charged area on the other end

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5
Q

What initially breaks down dietary proteins in our stomach?

A

HCl and pepsin

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6
Q

What breaks down denatured proteins and peptides?

A

pancreatic enzymes

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7
Q

What is the acronym for essential AAs?

A

Try THis VIP MaLL

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8
Q

How many AAs are essential?

A

nine

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9
Q

What are the three ways the body can get nonessential amino acids?

A

tricarboxylic acid, glycolysis, from an essential SS

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10
Q

If the pH of a medium is higher than the pKa of the amino acid, what happens?

A

deprotonation (loss of H+)

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11
Q

What are the two main acidic AAs?

A

aspartate and glutamate

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12
Q

What causes the acidity in aspartate and glutamate?

A

another carboxyl acid added

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13
Q

What is the precursor AA that begins cysteine biosynthesis?

A

methionine

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14
Q

What does a deficiency in cystathionase cause?

A

cystathioninuria

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15
Q

What is the cause of homocysteinuria?

A

deficiency of CBS (increases homocysteine)

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16
Q

Which cysteine synthesis disease can cause neurologic and cardiovascular disease’;

A

homocysteinuria

17
Q

What causes the formation of cystine?

A

oxidation of cysteine, causing disulfide bonds

18
Q

What disease causes kidney stones?

A

cystinuria

19
Q

What is the precursor essential AA that makes tyrosine?

A

phenylalanine

20
Q

What is the simplest AA?

A

glycine (non-polar)

21
Q

What are the two sulfur-containing AAs?

A

methionine and cysteine

22
Q

What type of AA is water solubles?

A

polar

23
Q

Which AAs do not have oxygen in their side chains?

A

non-polar (aliphatic)

24
Q

What molecular group in AAs can be easily protonated?

A

amino group (NH)

25
Q

What are the three aromatic AAs?

A

phenylalanine (e), tyrosine (ne), and tryptophan (e)

26
Q

What causes phenylketonuria (PKU)

A

defect of phenylalanine hydroxylase or defect of co-factor (dihydropteridine reductase)

27
Q

Which pt modification attaches a carbohydrate to an AA?

A

glycosylation

28
Q

Which pt modification adds a lipid molecule to AAs?

A

fatty acylation

29
Q

Which pt modification occurs on lysine residues of histone protein in chromatin?

A

acetylation

30
Q

Which pt modification modifies glutamate to form gamma-carboxyl, and occurs in clotting proteins?

A

carboxylation

31
Q

Which pt modification transfers a phosphate group on the hydroxyl group of kinases?

A

phosphorylation

32
Q

What are the three main protein kinase key in phosphorylation?

A

serine, threonine, tyrosine

33
Q

Which pt modification adds a hydroxyl group to proline and is key in stabilizing collagen?

A

hydroxylation or oxidation