Amino Acids Flashcards

1
Q

Tryptophan

A

Aromatic

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2
Q

Leucine

A

Branched

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3
Q

Isoleucine

A

Branched

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4
Q

Which two amino acids are ketogenic?

A

Leucine and lysine

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5
Q

Which four amino acids are both glucogenic and ketogenic?

A

Tyrosine, isoleucine, phenylalanine, and tryptophan.

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6
Q

What are the two intracellular pathways for protein degradation?

A
  1. Ubiquination and degradation in the proteasome

2. Degradation in lysosomes

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7
Q

What are the two nitrogen sources that enter the urea cycle?

A

Free ammonia from breakdown of an amino acid and from aspartate.

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8
Q

Which amino acid produces NO?

A

Arginine

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9
Q

Which AAs contain sulfur?

A

Cysteine and methionine

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10
Q

SAM is a precursor for what?

A

Homocysteine

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11
Q

Which amino acids are aromatic?

A

Tryptophan, tyrosine, phenylalanine

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12
Q

What is the Keq of transamination reactions?

A

1 - concentration dependent

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13
Q

ALT catalyzes which reaction?

A

Alanine + alphaketoglutarate -> pyruvate + glutamate

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14
Q

AST catalyzes which reaction?

A

Aspartate + alphaketoglutarate -> OAA + glutamate

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15
Q

What is PLP’s role in transamination?

A

Coenzyme to aminotransferases. Holds the N nearby.

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16
Q

PLP is a derivative of what?

A

Vit B6

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17
Q

Write out the overall reaction of the urea cycle

A

3ATP+HCO3+NH4+aspartate -> 2ADP+AMP+2Pi+PPi+fumarate+urea

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18
Q

What stimulates glutamate dehydrogenase and what inhibits it?

A

(+) ADP and GDP

(-) ATP and GTP

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19
Q

Write out the overall reaction of the urea cycle

A

3ATP+HCO3+NH4+aspartate -> 2ADP+AMP+2Pi+PPi+fumarate+urea

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20
Q

Which disease is associated with a deficiency in alpha ketoacid dehydrogenase complex?

21
Q

Which enzyme decarboxylates branched chain AAs?

A

alpha ketoacid dehydrogenase complex

22
Q

Which disease is associated with a deficiency in alpha ketoacid dehydrogenase complex?

23
Q

Tryptophan metabolism results in the formation of what?

A

Niacin, serotonin, melotonin

24
Q

Phenylalanine metabolism results in the formation of what?

A

Tyrosine, L-dopa, dopamine, melanin, NE, and epi

25
Glycine metabolism results in the formation of what?
Porphyrin and heme
26
Glutamate metabolism results in the formation of what?
GABA and glutathione
27
Arginine metabolism results in the formation of what?
NO, creatine phosphate, and urea
28
What can cysteine do?
Form disulfide bridges that change protein conformation
29
How can ammonia be transported to the liver for urea cycle?
Glutamine synthase can convert glutamate to glutamine to be transported to the liver.
30
What does muscle use to transport nitrogen?
Alanine instead of glutamine - due to buildup of pyruvate in muscle which can be converted to alanine with ALT
31
Which amino acid is associated with GSH?
Cysteine
32
SAM is a breakdown product of which AA?
Methionine
33
What are the starting and ending points of purine biosynthesis?
Ribose 5P -> IMP
34
What are the two key steps of purine biosynthesis?
PRPP synthetase and GPPA (glutamine phosphoribosyl pyrophosphate aminotransferase)
35
What are the activators and inhibitors of PRPP synthetase?
(+) Pi | -) purines, AMP, GMP, IMP (end-product inhibition
36
What are the activators and inhibitors of GPPA?
(+) PRPP | (-) AMP, GMP, IMP
37
What are the sources of atoms for purine synthesis?
Glutamine, glycine, aspartate, THF, CO2
38
What are the starting and ending points of pyrimidine synthesis?
2ATP + CO2 + glutamine -> UMP
39
What is the key enzymatic step of pyrimidine synthesis?
CPS II
40
What are the activators and inhibitors of CPS II?
(+) ATP, PRPP | (-) UTP
41
What are the sources of atoms for pyrimidine synthesis?
CO2, glutamine, aspartate, ribose sugar added last
42
What is a major difference between pyrimidine and purine biosynthesis?
In purine synthesis, the base is built onto the sugar. In pyrimidine synthesis, the complete base is added onto the sugar at the end.
43
Which enzyme converts RNA to DNA?
Ribonucleotide reductase
44
What is an inhibitor of ribonucleotide reductase?
dATP
45
On which phosphate form does ribonucleotide reductase act on exclusively?
Di-phosphate form
46
What does thymine break down to?
Succinyl-CoA
47
What does cytosine break down to?
Malonyl-CoA
48
What does uracil break down to?
Acetyl-Coa