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 Which of the following amino acids is considered as both ketogenic and glucogenic? Tryptophan None of these Valine Lysine Tryptophan None of these Valine Lysine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of the oxidative deamination is aspartate + hexanoic acid = glutamate + Oxaloacetate glutamate = α-ketoglutarate + NH3 glutamate = hexanoic acid + NH3 aspartate + α-ketoglutarate = glutamate + oxaloacetate aspartate + hexanoic acid = glutamate + Oxaloacetate glutamate = α-ketoglutarate + NH3 glutamate = hexanoic acid + NH3 aspartate + α-ketoglutarate = glutamate + oxaloacetate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria cannot convert phenylalanine to tyrosine phenylalanine to lysine phenylalanine to isoleucine phenol into ketones phenylalanine to tyrosine phenylalanine to lysine phenylalanine to isoleucine phenol into ketones ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Transamination is the transfer of an amino group from an amino acid to a keto acid acid to a keto acid plus ammonia acid to a carboxylic acid plus ammonia group from an amino acid to a carboxylic acid group from an amino acid to a keto acid acid to a keto acid plus ammonia acid to a carboxylic acid plus ammonia group from an amino acid to a carboxylic acid ANSWER DOWNLOAD EXAMIANS APP
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
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