The primary purpose of amino acid catabolism is to generate energy in the form of ATP. This process occurs when amino acids are broken down into smaller molecules, which are then oxidized to release energy.

Glycolysis is not a type of amino acid catabolism. It is a metabolic pathway that breaks down glucose to generate energy.

The first step in the catabolism of most amino acids is transamination, which involves the transfer of an amino group from the amino acid to a keto acid, resulting in the formation of a new amino acid and a new keto acid.

Glutamate dehydrogenase catalyzes the oxidative deamination of glutamate, converting it to α-ketoglutarate and ammonia.

The end product of the catabolism of most amino acids is acetyl-CoA, which can be further oxidized in the citric acid cycle to generate energy.

Arginine is catabolized to form urea, which is the primary nitrogenous waste product in humans.

The glutamate-α-ketoglutarate cycle is a metabolic pathway that converts glutamate to α-ketoglutarate, which can then be further oxidized in the citric acid cycle to generate energy.

Alanine is catabolized to form pyruvate, which can then be further oxidized in the citric acid cycle to generate energy.

Amino acid decarboxylase is the enzyme that catalyzes the decarboxylation of amino acids, removing a carboxyl group and releasing carbon dioxide.

Aspartate is catabolized to form oxaloacetate, which can then be further oxidized in the citric acid cycle to generate energy.

Phenylketonuria is a disorder that results from a deficiency of phenylalanine hydroxylase, an enzyme that converts phenylalanine to tyrosine. This deficiency leads to the accumulation of phenylalanine in the blood and urine.

Methionine is catabolized to form succinyl-CoA, which can then be further oxidized in the citric acid cycle to generate energy.

Maple syrup urine disease is a disorder that results from a deficiency of branched-chain ketoacid dehydrogenase, an enzyme that catalyzes the decarboxylation of branched-chain amino acids. This deficiency leads to the accumulation of branched-chain amino acids and their corresponding ketoacids in the blood and urine.

Arginine is catabolized to form fumarate, which can then be further oxidized in the citric acid cycle to generate energy.

Argininemia is a disorder that results from a deficiency of arginase, an enzyme that catalyzes the hydrolysis of arginine to form urea and ornithine. This deficiency leads to the accumulation of arginine in the blood and urine.