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