Amino Acid Metabolism A person with phenylketonuria cannot convert phenylalanine to tyrosine phenylalanine to isoleucine phenol into ketones phenylalanine to lysine phenylalanine to tyrosine phenylalanine to isoleucine phenol into ketones phenylalanine to lysine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A best described ketogenic amino acid is valine lysine none of these tryptophan valine lysine none of these tryptophan ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A ketogenic amino acid is one which degrades to either acetyl CoA or acetoacetyl CoA pyruvate or citric acid cycle intermediates multiple intermediates including pyruvate or citric acid cycle intermediates and acetyl CoA or acetoacetyl CoA keto-sugars either acetyl CoA or acetoacetyl CoA pyruvate or citric acid cycle intermediates multiple intermediates including pyruvate or citric acid cycle intermediates and acetyl CoA or acetoacetyl CoA keto-sugars ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Lysine is degraded to acetoacetyl CoA and is described as a ketogenic amino acid glucogenic amino acid none of these keto-gluco amino acid ketogenic amino acid glucogenic amino acid none of these keto-gluco amino acid ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A glucogenic amino acid is one which is degraded to either acetyl CoA or acetoacetyl CoA pyruvate or citric acid cycle intermediates keto-sugars None of these either acetyl CoA or acetoacetyl CoA pyruvate or citric acid cycle intermediates keto-sugars None of these ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of a transamination process is glutamate = hexanoic acid + NH3 aspartate + hexanoic acid = glutamate + oxaloacetate aspartate + α ketoglutarate = glutamate + oxaloacetate glutamate = α-ketoglutarate + NH3 glutamate = hexanoic acid + NH3 aspartate + hexanoic acid = glutamate + oxaloacetate aspartate + α ketoglutarate = glutamate + oxaloacetate glutamate = α-ketoglutarate + NH3 ANSWER DOWNLOAD EXAMIANS APP
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