Amino Acid Metabolism Flashcards

1
Q

The glucogenic amino acids’ catabolism yield which molecules?

A

Pyruvate, Oxaloacetate, alpha-ketogluterate, fumarate, succinyl-CoA,

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2
Q

The ketogenic amino acids’ catabolism yield which molecules?

A

Acetyl-CoA, Acetoacetate

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3
Q

Which amino acids are exclusively ketogenic?

A

Leucine and lysine

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4
Q

If there is a methionine deficiency what amino acid becomes conditionally essential?

A

Cysteine

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5
Q

If there is a phenylalanine deficiency what amino acid becomes conditionally essential?

A

Tyrosine

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6
Q

What vitamin is the precursor of tetrahydrofolate

A

Vitamin B9- Folic acid

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7
Q

What enzyme reduces folic acid to its active form?

A

Dihydrofolate reductase?

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8
Q

What is the action of Methotraxate?

A

It binds dihydrofolate reductase and competes with folate, so THF is not formed, which stops synthesis of DNA, RNA, and proteins

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9
Q

What conditions can folate deficiency lead to?

A

Megaloblastic anemia, anencephaly, spina bifida

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10
Q

What enzyme converts L-methionine to S-adenosylmethionine?

A

S-adenosylmethionine synthetase

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11
Q

What neurotransmitter synthesis requires SAM? What is the precursor? What is the structure resulting from SAM?

A

Epinephrine from norepinephrine yielding S-adenosylhomocysteine

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12
Q

What vitamin is biotin

A

B7

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13
Q

What kind of reaction is biotin used for?

A

Transfer of one carbon group in the form of CO2

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14
Q

What is the medical utility of Asparaginase? How does it work?

A

Anti-cancer drug for leukemia; Asparagine is essential for leukemia cells- asparaginase lowers levels of asparagine

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15
Q

What is the alpha-keto acid of alanine?

A

Pyruvate

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16
Q

What enzyme is deficient in homocystinuria?

A

Cystathione beta-synthase