Amino Acid Metabolism Histidine is degraded to α-ketoglutarate and is described as a ketogenic amino acid keto-gluco amino acid gluco amino acid glucogenic amino acid ketogenic amino acid keto-gluco amino acid gluco amino acid glucogenic amino acid ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of the oxidative deamination is aspartate + α-ketoglutarate = glutamate + oxaloacetate 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 ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Lysine is degraded to acetoacetyl CoA and is described as a keto-gluco amino acid glucogenic amino acid ketogenic amino acid none of these keto-gluco amino acid glucogenic amino acid ketogenic amino acid none of these ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism The most toxic compounds is tyrosine phenylpyruvate phenylalanine lysine tyrosine phenylpyruvate phenylalanine lysine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person suffering from phenylketonuria on consumption food containing high phenylalanine may lead to the accumulation of phenylalanine tyrosine phenylpyruvate isoleucine phenylalanine tyrosine phenylpyruvate isoleucine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria cannot convert phenylalanine to isoleucine phenylalanine to lysine phenylalanine to tyrosine phenol into ketones phenylalanine to isoleucine phenylalanine to lysine phenylalanine to tyrosine phenol into ketones ANSWER DOWNLOAD EXAMIANS APP
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