A. Dopamine to nor epinephrine

C. Phenylalanine to tyrosine

D. Dopa to dopamine

A. Hydrolase

B. Cytochrome oxidase

C. Dehydrogenase

A. Apo A-II

B. Apo C-III

D. Apo B-II

B. Epinephrine

C. Cortisone

D. GH

B. Phenyl alanine

C. None of the above

D. Tryptophan

A. Activate the substrate

C. Increase the active sites of apoenzyme

D. Enhance the specificity of apoenzyme

A. Hyperuricemia

B. Increased mobilization of glycogen from liver

C. Defective cori cycle

A. Alpha ketoglutarate dehydrogenase

C. Transaldolase

D. Pyruvate dehydrogenase

A. Enzymes

C. Minerals

D. Vitamins

A. Tyrosine

B. Phenylalanine

C. Epinephrine

A. Cytochrome P 450

B. Cytochromes

C. Super oxide dismutase

A. Tyrosine kinase

C. Polymerase

D. ATP synthase

A. 4

B. 1

C. 3

A. Phosphohexose isomerase

C. Succinate thiokinase

D. Lactate dehydrogenase

B. Embden-Meyerhof Pathway and H.M.P shunt

C. Glycogenolysis and Gluconeogenesis

D. Glycogenolysis and Citric and cycle

A. Pyruvate Kinase

B. ATPase

D. Fructose 6 phosphatase

A. Oxidases

B. Anticholinesterases

C. Cholinesterase

A. Thyroxine

C. Serotonin

D. Triidothyronine

A. II

B. III

C. IV

A. Give sigmoid shaped curve

B. Presence of Modulator site

D. They are multienzyme complex

A. Glucose 1 phosphate dehydrogenase

B. Glucose 1,6 diphosphate dehydrogenase

D. All of the above

A. Zymogen

C. Coenzyme

D. Antienzyme

A. Nucleolus

B. Mitochondria

C. Plasma membrane

A. Absence of glucokinase

B. Muscle does not contain glycogen phosphorylase

D. Muscle lacks phospho gluco isomerase

A. 7.7 8.0

B. 7.0 7.12

C. 6.8 7.0

B. Acetyl CoA

C. ATP

D. ADP

A. Methyl testosterone

C. Estrogen

D. Aldosterone

A. Hexokinase

C. Phosphohexose isomerase

D. Enolase

A. Protoenzyme

B. Apoenzyme

D. Proenzyme

B. 4 5.5 mg%

C. 1 3 mg%

D. 3 4 mg%

A. Malonyl CoA synthetase

B. HMG-Co A synthase

C. Fatty acid synthetase

A. Smell of acetone in breath

B. Metabolic acidosis

C. Rotheras test is +ve

A. Apoenzyme

B. Coenzyme

C. Constitutive enzyme

B. Symmertrical bi leaflet structures

C. Rigid assembly of protein, lipid and carbohydrate

D. Lipid and protein moiety are held by covalent interactions

A. Glucose 6 phosphatase

B. Glucose 1,6 diphosphatase

D. Fructose 1- phosphatase

B. Succinate

C. Fumarate

D. Isocitrate

A. It is a ketose

B. It possessesan anomeric C-2 carbon atom

C. It usually exists in the furanose form

A. Protein syntehsis

B. Fatty acid synthesis

D. Glycogen synthesis

A. 3

B. 11

C. 2

A. Substrate protiens

C. Structural proteins

D. Polymer

A. G-6-P dehydrogenase

B. Glucokinase

D. Aldolase

A. TTP

B. ATP

D. ITP

A. Deficiency of glutamic acid

C. Deficiency of oxaloacetic acid

D. All of the above

A. Haemoglobin

B. Gall bladder

C. Myoglobin

A. Endoplasmic reticulum

B. Golgi body

C. Ribosome

A. Albumin

C. Globulin

D. Hemoglobin

A. Thiamine Acyl CoA

C. Biotin-CO2

D. ATP-Hydrogen

A. Lebers neuropathy

C. Gauchers disease

D. Epidermolysis bullosa

A. Alpha galactosidase

C. Muscle phosphorylase

D. Acid Lipase

A. GLUT-2 stimulated by insulin

B. Glucokinase has a low Km for glucose

D. Hexokinase in liver has a high affinity for glucose