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 best described ketogenic amino acid is valine lysine tryptophan none of these valine lysine tryptophan none of these ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of the oxidative deamination is 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 aspartate + α-ketoglutarate = glutamate + oxaloacetate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Transaminase enzymes are present in liver pancreas none of these intestine liver pancreas none of these intestine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism The most toxic compounds is phenylalanine tyrosine phenylpyruvate lysine phenylalanine tyrosine phenylpyruvate lysine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Lysine is degraded to acetoacetyl CoA and is described as a glucogenic amino acid none of these ketogenic amino acid keto-gluco amino acid glucogenic amino acid none of these ketogenic amino acid keto-gluco amino acid ANSWER DOWNLOAD EXAMIANS APP
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