Amino Acid Metabolism A ketogenic amino acid is one which degrades to multiple intermediates including pyruvate or citric acid cycle intermediates and acetyl CoA or acetoacetyl CoA either acetyl CoA or acetoacetyl CoA keto-sugars pyruvate or citric acid cycle intermediates multiple intermediates including pyruvate or citric acid cycle intermediates and acetyl CoA or acetoacetyl CoA either acetyl CoA or acetoacetyl CoA keto-sugars pyruvate or citric acid cycle intermediates ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of the oxidative deamination is aspartate + α-ketoglutarate = glutamate + oxaloacetate 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 ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Tyrosine is degraded to acetoacetyl CoA and fumarate and is described as a keto-gluco amino acid ketogenic and glucogenic amino acid glucogenic amino acid ketogenic amino acid keto-gluco amino acid ketogenic and glucogenic amino acid glucogenic amino acid ketogenic amino acid 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 The most toxic compounds is phenylpyruvate phenylalanine tyrosine lysine phenylpyruvate phenylalanine tyrosine 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 tyrosine phenylpyruvate phenylalanine isoleucine tyrosine phenylpyruvate phenylalanine isoleucine ANSWER DOWNLOAD EXAMIANS APP
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