Amino Acid Metabolism A glucogenic amino acid is one which is degraded to keto-sugars either acetyl CoA or acetoacetyl CoA pyruvate or citric acid cycle intermediates None of these keto-sugars either acetyl CoA or acetoacetyl CoA pyruvate or citric acid cycle intermediates None of these ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Lysine is degraded to acetoacetyl CoA and is described as a ketogenic amino acid none of these glucogenic amino acid keto-gluco amino acid ketogenic amino acid none of these glucogenic amino acid keto-gluco amino acid ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria cannot convert phenol into ketones phenylalanine to lysine phenylalanine to tyrosine phenylalanine to isoleucine phenol into ketones phenylalanine to lysine phenylalanine to tyrosine phenylalanine to isoleucine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria will convert phenylpyruvate to phenylalanine phenylalanine to isoleucine tyrosine to phenylalanine phenylalanine to phenylpyruvate phenylpyruvate to phenylalanine phenylalanine to isoleucine tyrosine to phenylalanine phenylalanine to phenylpyruvate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism In the normal breakdown of phenylalanine, it is initially degraded to lysine fumarate tyrosine phenylpuruvate lysine fumarate tyrosine phenylpuruvate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of a transamination process is aspartate + hexanoic acid = glutamate + oxaloacetate glutamate = α-ketoglutarate + NH3 glutamate = hexanoic acid + NH3 aspartate + α ketoglutarate = glutamate + oxaloacetate aspartate + hexanoic acid = glutamate + oxaloacetate glutamate = α-ketoglutarate + NH3 glutamate = hexanoic acid + NH3 aspartate + α ketoglutarate = glutamate + oxaloacetate ANSWER DOWNLOAD EXAMIANS APP