Amino Acid Metabolism Tyrosine is degraded to acetoacetyl CoA and fumarate and is described as a 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 ketogenic and glucogenic amino acid ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Transaminase enzymes are present in liver intestine none of these pancreas liver intestine 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 + hexanoic acid = glutamate + Oxaloacetate glutamate = hexanoic acid + NH3 aspartate + α-ketoglutarate = glutamate + oxaloacetate glutamate = α-ketoglutarate + NH3 aspartate + hexanoic acid = glutamate + Oxaloacetate 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 tyrosine lysine fumarate phenylpuruvate tyrosine lysine fumarate phenylpuruvate ANSWER DOWNLOAD EXAMIANS APP
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