Amino Acid Metabolism In the normal breakdown of phenylalanine, it is initially degraded to lysine tyrosine fumarate phenylpuruvate lysine tyrosine fumarate phenylpuruvate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of a transamination process is glutamate = hexanoic acid + NH3 aspartate + hexanoic acid = glutamate + oxaloacetate glutamate = α-ketoglutarate + NH3 aspartate + α ketoglutarate = glutamate + oxaloacetate glutamate = hexanoic acid + NH3 aspartate + hexanoic acid = glutamate + oxaloacetate glutamate = α-ketoglutarate + NH3 aspartate + α ketoglutarate = glutamate + oxaloacetate ANSWER DOWNLOAD EXAMIANS APP
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 Histidine is degraded to α-ketoglutarate and is described as a keto-gluco amino acid glucogenic amino acid gluco amino acid ketogenic amino acid keto-gluco amino acid glucogenic amino acid gluco amino acid ketogenic amino acid 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 Tyrosine is degraded to acetoacetyl CoA and fumarate and is described as a glucogenic amino acid ketogenic and glucogenic amino acid keto-gluco amino acid ketogenic amino acid glucogenic amino acid ketogenic and glucogenic amino acid keto-gluco amino acid ketogenic amino acid ANSWER DOWNLOAD EXAMIANS APP
EXAMIANS