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Pyruvate dehydrogenase complex: The bridge between aerobic glycolysis and citric acid cycle.

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Glycine Metabolism
The (1) endogenous production, (2) uptake of dietary glycine, and (3) renal reabsorption are the main sources of glycine in humans.

Members are included in the TCA Cycle:
1. Citrate.
2. Isocitrate.
3. Alpha ketoglutarate.
4. Succinyl CoA.
5. Succinate.
6. Fumarate.
7. Malate.
8. Oxaloacetate.

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Classes of enzymes:
1. Hydrolases.
2. Oxidoreductases.
3. Lyases.
4. Transferases.
5. Ligases.
6. Isomerases.

Coenzymes are required by pyruvate dehydrogenase complex:
1. FAD
2. NAD.
3. CoA.
4. Lipoic acid.
5. TPP (vitamin B1).

Steps in beta oxidation of fatty acids:
1. Oxidation.
2. Hydration.
3. Oxidation.
4. Cleavage.

Steps in amino acid catabolism:
1. Transamination.
2. Oxidative deamination.
3. Urea cycle.

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