HMG-CoA is formed during metabolism of all except______________?

Related Mcqs:

1. HMG CoA reductase is inhibited by_____________?

   A. Clofibrate
   B. Gemfibrosil
   C. Lovastatin
   D. cholestyramine

2. Which is not seen in HMG CoA pathway ?

   A. Pyruvate
   B. Cholesterol
   C. Mevalonate
   D. Acetyl CoA

3. Acetyl CoA is produced from which fuel sources_____________?

   A. Carbohydrate
   B. Lipid
   C. Amino acids
   D. All of the above

4. Direct filling gold formed by electrolytic precipitation is called by all the terms EXCEPT______________?

   A. Crystalline
   B. Granular gold
   C. Mat gold
   D. Sponge gold

5. Ketone bodies are by products of metabolism of_____________?

   A. Carbohydrate
   B. Protein
   C. Fat
   D. All of the above

6. All the following causes the secretion of gastric juice during cephalic phase EXCEPT______________?

   A. Food in the mouth
   B. Sight of food
   C. Food in the stomach
   D. Thought of food

7. Which vitamin is related to a co-factor in glycine metabolism is______________?

   A. Vit E
   B. Folic acid
   C. Thiamine
   D. Cobalamine

8. Alkaptonuria, an inherited metabolic disorder of L0tyrosine metabolism is due to lack of_____________?

   A. Parahydroxy phenyl pyruvate Hydroxylase
   B. Tyrosine transaminase
   C. Homogentisate oxidase
   D. Tyrosine oxidase

9. Albinism is a genetic disease that results in incomplete metabolism of______________?

   A. Histidine
   B. Cystine
   C. Tyrosine
   D. Alanine

10. In the body, metabolism of 10 g of protein would produce approximately____________?

    A. 1 Kcal
    B. 41 Kcal
    C. 410 Kcal
    D. 4100 Kcal