Amino Acid Metabolism Lysine is degraded to acetoacetyl CoA and is described as a none of these ketogenic amino acid glucogenic amino acid keto-gluco amino acid none of these ketogenic amino acid glucogenic amino acid keto-gluco amino acid 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 tyrosine isoleucine phenylpyruvate phenylalanine tyrosine isoleucine phenylpyruvate 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 The most toxic compounds is lysine phenylalanine phenylpyruvate tyrosine lysine phenylalanine phenylpyruvate tyrosine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of the oxidative deamination is aspartate + α-ketoglutarate = glutamate + oxaloacetate glutamate = hexanoic acid + NH3 glutamate = α-ketoglutarate + NH3 aspartate + hexanoic acid = glutamate + Oxaloacetate aspartate + α-ketoglutarate = glutamate + oxaloacetate glutamate = hexanoic acid + NH3 glutamate = α-ketoglutarate + NH3 aspartate + hexanoic acid = glutamate + Oxaloacetate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Histidine is degraded to α-ketoglutarate and is described as a keto-gluco amino acid ketogenic amino acid gluco amino acid glucogenic amino acid keto-gluco amino acid ketogenic amino acid gluco amino acid glucogenic amino acid ANSWER DOWNLOAD EXAMIANS APP
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