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 A person suffering from phenylketonuria on consumption food containing high phenylalanine may lead to the accumulation of isoleucine phenylpyruvate tyrosine phenylalanine isoleucine phenylpyruvate tyrosine phenylalanine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Transaminase enzymes are present in pancreas none of these liver intestine pancreas none of these liver intestine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A glucogenic amino acid is one which is degraded to pyruvate or citric acid cycle intermediates keto-sugars either acetyl CoA or acetoacetyl CoA None of these pyruvate or citric acid cycle intermediates keto-sugars either acetyl CoA or acetoacetyl CoA None of these ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A best described ketogenic amino acid is valine none of these lysine tryptophan valine none of these lysine tryptophan 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
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