Amino Acid Metabolism A person with phenylketonuria will convert phenylalanine to isoleucine tyrosine to phenylalanine phenylalanine to phenylpyruvate phenylpyruvate to phenylalanine phenylalanine to isoleucine tyrosine to phenylalanine phenylalanine to phenylpyruvate phenylpyruvate to phenylalanine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Which of the following amino acids is considered as both ketogenic and glucogenic? None of these Lysine Valine Tryptophan None of these Lysine Valine Tryptophan ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of the oxidative deamination is glutamate = hexanoic acid + NH3 glutamate = α-ketoglutarate + NH3 aspartate + α-ketoglutarate = glutamate + oxaloacetate aspartate + hexanoic acid = glutamate + Oxaloacetate glutamate = hexanoic acid + NH3 glutamate = α-ketoglutarate + NH3 aspartate + α-ketoglutarate = glutamate + oxaloacetate aspartate + hexanoic acid = glutamate + Oxaloacetate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism In the normal breakdown of phenylalanine, it is initially degraded to lysine tyrosine phenylpuruvate fumarate lysine tyrosine phenylpuruvate fumarate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism The most toxic compounds is phenylalanine tyrosine lysine phenylpyruvate phenylalanine tyrosine lysine phenylpyruvate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Tyrosine is degraded to acetoacetyl CoA and fumarate and is described as a ketogenic amino acid keto-gluco amino acid glucogenic amino acid ketogenic and glucogenic amino acid ketogenic amino acid keto-gluco amino acid glucogenic amino acid ketogenic and glucogenic amino acid ANSWER DOWNLOAD EXAMIANS APP
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