A. UTP
B. GTP
C. Pyruvate Kinase
D. Guanosine
Related Mcqs:
- Blood glucose level cannot be augmented by mobilization of muscle glycogen due to lack of_____________?
A. G-6-P dehydrogenase
B. G-6-P phydrogenase
C. Aldolase
D. Glucokinase - Muscle glycogen, which cannot contribute to blood glucose due to the absence of which enzymes ?
A. Phosphoglutamase
B. Branching enzyme
C. Debranching enzyme
D. Glucose-6-phosphotase - Muscle glycogen cannot contribute directly to blood glucose level because___________?
A. Muscle lacks glucose 6 phosphatase
B. Muscle lacks phospho gluco isomerase
C. Absence of glucokinase
D. Muscle does not contain glycogen phosphorylase - Number of ATP molecules generated in the conversion of glycogen of lactate is_____________?
A. 2
B. 36
C. 38
D. 32 - The uptake of glucose by the liver increase following a carbohydrate meal because____________?
A. There is increase in phosphorylation of glucose by glucokinase
B. GLUT-2 stimulated by insulin
C. Glucokinase has a low Km for glucose
D. Hexokinase in liver has a high affinity for glucose - The conversion of glucose 6-P to fructose 6-P is an example of which of the following reactions___________?
A. Phosphate transfer
B. Isomerisation
C. Dehydration
D. Aldol cleavage - A child’s CSF was examined I contains slightly raised or normal PMN cells, raised lymphocytes, absence of mycotic growth, value of protein is normal or above normal, glucose level is normal. The most probable diagnosis is____________?
A. Pyogenic bacterial meningitis
B. Viral meningitis
C. Fungal meningitis
D. Tuberculous meningitis - Glycogen breakdown leads to formation of______________?
A. Glucose
B. Lactic acid
C. Glucose & Lactic acid
D. Glycoprotein - The tissue with the highest glycogen content (mg/100gm)_____________?
A. Liver
B. Muscle
C. Kidneys
D. Testes - Type II glycogen storage disorder is due to deficiency of______________?
A. Alpha -Glucosidase
B. Alpha galactosidase
C. Muscle phosphorylase
D. Acid Lipase
