Biochemistry flashcards
Biochemistry flashcard decks shared publicly by Klappa users: metabolism, enzymes, lipids, carbohydrates, amino acids and bioenergetics. 60 decks, 5435 cards in all. Open a deck to read every card without an account, then sign in to study it with spaced repetition.
- 11 · PTH Actions on Bone, Kidney & Gut (and the Calcitriol/FGF-23 Axis)
- 5.) Carbohydrate metabolism Part 1
- 2.) Mitochondrial respiratory chain and oxidative phosphorylation
- Enzymes: Catalysis and Classification
- 13.1 - Introduction, Phosphorylation of Glucose
- 12.3 - Flow of Electrons
- Fatty Acid Synthesis
- Chemistry, pH & Buffers
- Lipids Foundations
- 12.5 - TCA Cycle
- 13.4 - Regulation of Glycolysis
- 13.3 - PDH
- 13.2 - Glycolysis, Reactions, Fate of Pyruvate
- 12.4 - ATP Synthase
- 15.4 - De novo synthesis of lipids: Saturated and Unsaturated FFA, complex lipids
- 15.2 - Lipid stores as energy sourrce: FFA
- Carbohydrates — Structure, Digestion & Absorption
- Heme: Synthesis, Degradation, Jaundice, and Iron
- 15.3 - Lipid stores as energy source: Ketone bodies
- Glycolysis
- The Pentose Phosphate Pathway
- 14.) Lipoproteins: structure, components, roles of apoproteins (apo A1, Apo B48 and apo B100, apo CII, apo E), metabolism of chylomicrons, VLDL, HDL. Increased LDL/HDL ratio as a risk factor for atherosclerosis. Deficiency/defects of LPL, apo CII, LDL receptor and apo B100 and their consequences.
- Metabolic Integration — Fed, Fasting, and Starvation
- Enzyme Kinetics & Inhibition
- Calcium, Phosphorus & Biomineralization
- Proteins, Hemoglobin, and Plasma Proteins
- Bioenergetics, the TCA Cycle & Oxidative Phosphorylation
- Eicosanoids
- The Urea Cycle
- Ketone Bodies
- 10.) Pentose phosphate pathway. Reversible and irreversible reactions of the pathway. Oxidative arm - dehydrogenases reactions, role as a source of NADPH (functions of NADPH!) and ribose-5P. Non-oxidative arm role/importance. Consequences of G6P dehydrogenase deficiency.
- Amino-Acid Metabolism: PLP, One-Carbon, PKU & B12
- Extracellular Matrix and Oral Biochemistry
- Nucleotide Metabolism, Purine Degradation & Gout
- Amino-Acid Catabolism: Transamination and Ammonia
- 8.) Part 2 - Differences between liver and muscle cells concerning glycogen metabolism. Inherited defects of glycogen degradation (von Gierke’s disease, Mc Ardle syndrome).
- Cholesterol and Its Derivatives
- Glycogen Metabolism: Liver vs Muscle
- β-Oxidation of Fatty Acids
- 8.) Part 1 - Glycogen: reactions of glycogen synthesis and degradation, regulation (phosphorylation cascade, allosteric effectors, role of AMP and calcium ions)
- 4.) Carbohydrates Structure
- 16.2 - Complex lipid synthesis and defects accompanying their degradation
- Amino Acids
- Pyruvate, oxaloacetate, acetyl-CoA as key metabolites:
- 16.4 - Transport of cholesterol in the body
- 3.) The tricarboxylic acid cycle (TCA).
- 7.) PDH complex
- 5.) Carbohydrate metabolism part 2
- 13.) Fatty acid activation to acyl-CoA – reaction, its importance in lipid metabolism.
- 9.) Metabolism of fructose and galactose. Inherited defects (fructosuria, fructose intolerance, galactosemia.
- 11.) Lipids: structures of major lipids: triacylglycerols (TAG), phosphatidylserine, phosphatidylcholine, sphingomyelin, cholesterol and its main derivatives. Lipid soluble vitamins.
- 12.) Lipases: pancreatic, lipoprotein, hormone sensitive – their localization and roles, activating factors. Digestion and absorption of lipids in the GI tract.
- 16.1 - Metabolic fate of fatty acids
- 16.3 - Synthesis of Cholesterol
- 15.) Fatty acid degradation: intracellular localization, role of carnitine, reactions, ATP produced, regulation (role of carnitine palmitoyltransferase I). Fates of propionyl CoA.
- Reactive Oxygen Species and Antioxidant Defense
- Gluconeogenesis
- 16.5 - cholesterol derivatives, pages 45-59
- Detoxification & Xenobiotics
- Lipoproteins and Lipid Transport
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