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Amino Acid Metabolism

Amino Acid Metabolism
In the normal breakdown of phenylalanine, it is initially degraded to

lysine
tyrosine
phenylpuruvate
fumarate

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Amino Acid Metabolism
A person suffering from phenylketonuria on consumption food containing high phenylalanine may lead to the accumulation of

tyrosine
isoleucine
phenylalanine
phenylpyruvate

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Amino Acid Metabolism
Oxidative deamination is the conversion of an amino

group from an amino acid to a keto acid
acid to a carboxylic acid plus ammonia
group from an amino acid to a carboxylic acid
acid to a keto acid plus ammonia

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Amino Acid Metabolism
A person with phenylketonuria is advised not to consume which of the following products?

Aspartame
Fat containing food
Glucose
Glycine containing foods

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Amino Acid Metabolism
Tyrosine is degraded to acetoacetyl CoA and fumarate and is described as a

ketogenic and glucogenic amino acid
keto-gluco amino acid
ketogenic amino acid
glucogenic amino acid

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Amino Acid Metabolism
Histidine is degraded to α-ketoglutarate and is described as a

glucogenic amino acid
keto-gluco amino acid
gluco amino acid
ketogenic amino acid

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MORE MCQ ON Amino Acid Metabolism

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