Amino Acid Metabolism Tyrosine is degraded to acetoacetyl CoA and fumarate and is described as a ketogenic and glucogenic amino acid ketogenic amino acid glucogenic amino acid keto-gluco amino acid ketogenic and glucogenic amino acid ketogenic amino acid glucogenic amino acid keto-gluco amino acid ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Transaminase enzymes are present in none of these liver intestine pancreas none of these liver intestine pancreas ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria will convert phenylalanine to phenylpyruvate tyrosine to phenylalanine phenylpyruvate to phenylalanine phenylalanine to isoleucine phenylalanine to phenylpyruvate tyrosine to phenylalanine phenylpyruvate to phenylalanine phenylalanine to isoleucine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of the oxidative deamination is 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 glutamate = hexanoic acid + NH3 aspartate + hexanoic acid = glutamate + Oxaloacetate ANSWER DOWNLOAD EXAMIANS APP
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