Amino Acid Metabolism An example of the oxidative deamination is 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 aspartate + hexanoic acid = glutamate + Oxaloacetate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of a transamination process is aspartate + hexanoic acid = glutamate + oxaloacetate aspartate + α ketoglutarate = glutamate + oxaloacetate glutamate = hexanoic acid + NH3 glutamate = α-ketoglutarate + NH3 aspartate + hexanoic acid = glutamate + oxaloacetate aspartate + α ketoglutarate = glutamate + oxaloacetate glutamate = hexanoic acid + NH3 glutamate = α-ketoglutarate + NH3 ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Histidine is degraded to α-ketoglutarate and is described as a glucogenic amino acid gluco amino acid keto-gluco amino acid ketogenic amino acid glucogenic amino acid gluco amino acid keto-gluco amino acid ketogenic amino acid ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A best described ketogenic amino acid is none of these tryptophan valine lysine none of these tryptophan valine lysine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Lysine is degraded to acetoacetyl CoA and is described as a ketogenic amino acid keto-gluco amino acid none of these glucogenic amino acid ketogenic amino acid keto-gluco amino acid none of these glucogenic amino acid ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria will convert phenylpyruvate to phenylalanine phenylalanine to phenylpyruvate phenylalanine to isoleucine tyrosine to phenylalanine phenylpyruvate to phenylalanine phenylalanine to phenylpyruvate phenylalanine to isoleucine tyrosine to phenylalanine ANSWER DOWNLOAD EXAMIANS APP
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