Amino Acid Metabolism Tyrosine is degraded to acetoacetyl CoA and fumarate and is described as a ketogenic and glucogenic amino acid ketogenic amino acid keto-gluco amino acid glucogenic amino acid ketogenic and glucogenic amino acid ketogenic amino acid keto-gluco amino acid glucogenic amino acid ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Transaminase enzymes are present in intestine liver none of these pancreas intestine liver none of these pancreas ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria will convert tyrosine to phenylalanine phenylpyruvate to phenylalanine phenylalanine to isoleucine phenylalanine to phenylpyruvate tyrosine to phenylalanine phenylpyruvate to phenylalanine phenylalanine to isoleucine phenylalanine to phenylpyruvate 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
Amino Acid Metabolism In the normal breakdown of phenylalanine, it is initially degraded to lysine fumarate phenylpuruvate tyrosine lysine fumarate phenylpuruvate tyrosine ANSWER DOWNLOAD EXAMIANS APP