Amino Acid Metabolism An example of the oxidative deamination is aspartate + α-ketoglutarate = glutamate + oxaloacetate 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 ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Tyrosine is degraded to acetoacetyl CoA and fumarate and is described as a ketogenic and glucogenic amino acid keto-gluco amino acid ketogenic amino acid glucogenic amino acid ketogenic and glucogenic amino acid keto-gluco amino acid ketogenic amino acid glucogenic amino acid ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria cannot convert phenylalanine to lysine phenylalanine to tyrosine phenol into ketones phenylalanine to isoleucine phenylalanine to lysine phenylalanine to tyrosine phenol into ketones phenylalanine to isoleucine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Lysine is degraded to acetoacetyl CoA and is described as a ketogenic amino acid none of these keto-gluco amino acid glucogenic amino acid ketogenic amino acid none of these keto-gluco amino acid glucogenic amino acid ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A glucogenic amino acid is one which is degraded to pyruvate or citric acid cycle intermediates None of these keto-sugars either acetyl CoA or acetoacetyl CoA pyruvate or citric acid cycle intermediates None of these keto-sugars either acetyl CoA or acetoacetyl CoA ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person suffering from phenylketonuria on consumption food containing high phenylalanine may lead to the accumulation of phenylalanine phenylpyruvate tyrosine isoleucine phenylalanine phenylpyruvate tyrosine isoleucine ANSWER DOWNLOAD EXAMIANS APP
EXAMIANS