Amino Acid Metabolism A person with phenylketonuria will convert phenylalanine to isoleucine tyrosine to phenylalanine phenylpyruvate to phenylalanine phenylalanine to phenylpyruvate phenylalanine to isoleucine tyrosine to phenylalanine phenylpyruvate to phenylalanine phenylalanine to phenylpyruvate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria is advised not to consume which of the following products? Glycine containing foods Aspartame Glucose Fat containing food Glycine containing foods Aspartame Glucose Fat containing food ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A ketogenic amino acid is one which degrades to multiple intermediates including pyruvate or citric acid cycle intermediates and acetyl CoA or acetoacetyl CoA pyruvate or citric acid cycle intermediates either acetyl CoA or acetoacetyl CoA keto-sugars multiple intermediates including pyruvate or citric acid cycle intermediates and acetyl CoA or acetoacetyl CoA pyruvate or citric acid cycle intermediates either acetyl CoA or acetoacetyl CoA keto-sugars ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism The most toxic compounds is phenylalanine tyrosine lysine phenylpyruvate phenylalanine tyrosine lysine phenylpyruvate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A best described ketogenic amino acid is lysine none of these valine tryptophan lysine none of these valine tryptophan ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of the oxidative deamination is glutamate = α-ketoglutarate + NH3 aspartate + α-ketoglutarate = glutamate + oxaloacetate aspartate + hexanoic acid = glutamate + Oxaloacetate glutamate = hexanoic acid + NH3 glutamate = α-ketoglutarate + NH3 aspartate + α-ketoglutarate = glutamate + oxaloacetate aspartate + hexanoic acid = glutamate + Oxaloacetate glutamate = hexanoic acid + NH3 ANSWER DOWNLOAD EXAMIANS APP
EXAMIANS