Step 1: Understanding hexokinase and glucokinase.
Hexokinase and glucokinase are two different enzymes involved in glucose metabolism. Hexokinase is found in almost all tissues and has a low \( K_m \) for glucose, meaning it has a high affinity for glucose. Glucokinase, however, is found in the liver and pancreas and has a higher \( K_m \), indicating a lower affinity for glucose.
Step 2: Analyzing the options.
(A) They are both ubiquitously present in all cells: This is incorrect. While hexokinase is found in nearly all tissues, glucokinase is primarily present in the liver and pancreas.
(B) They are isozymes: This is correct in a sense, as they catalyze the same reaction but differ in their properties and tissue distribution. However, this option doesn't explain the difference between hexokinase and glucokinase in terms of \( K_m \).
(C) They differ in their \( K_m \) for glucose: This is correct. Hexokinase has a lower \( K_m \) than glucokinase, reflecting their different affinities for glucose.
(D) They are identical in their primary structure: This is incorrect. Hexokinase and glucokinase have different primary structures, even though they perform similar functions.
Step 3: Conclusion.
The correct answer is (C) They differ in their \( K_m \) for glucose, as this directly explains the key functional difference between hexokinase and glucokinase.
Which one of the following matches is CORRECT between the inhibitors given in Group A with their modes of action in Group B?
\[\begin{array}{|c|c|} \hline Group A & Group B \\ \hline \text{(P) Antimycin A} & \text{(i) Inhibits cytochrome c oxidase} \\ \hline \text{(Q) Amytal} & \text{(ii) Blocks electron transfer from cyt b to cyt c1} \\ \hline \text{(R) Carbon monoxide} & \text{(iii) Inhibits adenine nucleotide translocase} \\ \hline \text{(S) Atractyloside} & \text{(iv) Prevents electron transfer from Fe-S centers of complex 1 to ubiquinone} \\ \hline \end{array}\]