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 The most toxic compounds is lysine phenylpyruvate phenylalanine tyrosine lysine phenylpyruvate phenylalanine tyrosine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A glucogenic amino acid is one which is degraded to 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 pyruvate or citric acid cycle intermediates ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A best described ketogenic amino acid is tryptophan valine none of these lysine tryptophan valine none of these lysine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Tyrosine is degraded to acetoacetyl CoA and fumarate and is described as a glucogenic amino acid 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 ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of the oxidative deamination is 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 glutamate = hexanoic acid + NH3 ANSWER DOWNLOAD EXAMIANS APP
EXAMIANS