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 Lysine is degraded to acetoacetyl CoA and is described as a keto-gluco amino acid none of these ketogenic amino acid glucogenic amino acid keto-gluco amino acid none of these ketogenic amino acid glucogenic amino acid ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria will convert tyrosine to phenylalanine phenylalanine to phenylpyruvate phenylpyruvate to phenylalanine phenylalanine to isoleucine tyrosine to phenylalanine phenylalanine to phenylpyruvate phenylpyruvate to phenylalanine phenylalanine to isoleucine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person suffering from phenylketonuria on consumption food containing high phenylalanine may lead to the accumulation of phenylpyruvate isoleucine tyrosine phenylalanine phenylpyruvate isoleucine tyrosine phenylalanine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Histidine is degraded to α-ketoglutarate and is described as a glucogenic amino acid ketogenic amino acid gluco amino acid keto-gluco amino acid glucogenic amino acid ketogenic amino acid gluco amino acid keto-gluco amino acid ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of the oxidative deamination is 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 glutamate = α-ketoglutarate + NH3 aspartate + hexanoic acid = glutamate + Oxaloacetate ANSWER DOWNLOAD EXAMIANS APP
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