Amino Acid Metabolism An example of the oxidative deamination is aspartate + α-ketoglutarate = glutamate + oxaloacetate 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 ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria cannot convert phenylalanine to isoleucine phenylalanine to tyrosine phenol into ketones phenylalanine to lysine phenylalanine to isoleucine phenylalanine to tyrosine phenol into ketones phenylalanine to lysine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Lysine is degraded to acetoacetyl CoA and is described as a none of these keto-gluco amino acid ketogenic amino acid glucogenic amino acid none of these keto-gluco amino acid ketogenic amino acid glucogenic amino acid ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of a transamination process is glutamate = α-ketoglutarate + NH3 aspartate + hexanoic acid = glutamate + oxaloacetate glutamate = hexanoic acid + NH3 aspartate + α ketoglutarate = glutamate + oxaloacetate glutamate = α-ketoglutarate + NH3 aspartate + hexanoic acid = glutamate + oxaloacetate glutamate = hexanoic acid + NH3 aspartate + α ketoglutarate = glutamate + oxaloacetate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria is advised not to consume which of the following products? Fat containing food Aspartame Glucose Glycine containing foods Fat containing food Aspartame Glucose Glycine containing foods ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Histidine is degraded to α-ketoglutarate and is described as a glucogenic amino acid keto-gluco amino acid ketogenic amino acid gluco amino acid glucogenic amino acid keto-gluco amino acid ketogenic amino acid gluco amino acid ANSWER DOWNLOAD EXAMIANS APP
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