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