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