Amino Acid Metabolism Histidine is degraded to α-ketoglutarate and is described as a keto-gluco amino acid ketogenic amino acid glucogenic amino acid gluco amino acid keto-gluco amino acid ketogenic amino acid glucogenic amino acid gluco amino acid ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A best described ketogenic amino acid is tryptophan lysine valine none of these tryptophan lysine valine none of these ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria cannot convert phenylalanine to tyrosine phenylalanine to isoleucine phenylalanine to lysine phenol into ketones phenylalanine to tyrosine phenylalanine to isoleucine phenylalanine to lysine 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 group from an amino acid to a carboxylic acid acid to a keto acid plus ammonia acid to a carboxylic acid plus ammonia group from an amino acid to a keto acid group from an amino acid to a carboxylic acid acid to a keto acid plus ammonia acid to a carboxylic acid plus ammonia ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of a transamination process is aspartate + hexanoic acid = glutamate + oxaloacetate 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 ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person suffering from phenylketonuria on consumption food containing high phenylalanine may lead to the accumulation of tyrosine phenylpyruvate isoleucine phenylalanine tyrosine phenylpyruvate isoleucine phenylalanine ANSWER DOWNLOAD EXAMIANS APP
EXAMIANS