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GATE 2026 BT Q.28: solution and answer

GATE 2026 · BTQ.28 · 1 mark · MSQ

Which of the following drugs inhibit(s) ATP-ADP translocase?

  1. (A)

    Oligomycin

  2. (B)

    Atractyloside

  3. (C)

    Amytal

  4. (D)

    Bongkrekic acid

See the question in the paper

Answer and solution

ANSWER

The ATP-ADP translocase is inhibited by atractyloside (B) and bongkrekic acid (D).

Official answer: B, DSource: Official answer key, GATE 2026 BT (IIT Guwahati)

  1. The ATP-ADP translocase (adenine nucleotide translocase, ANT) sits in the inner mitochondrial membrane. It exports from the matrix and imports in a 1:1 antiport.

  2. (A) Oligomycin binds the proton channel of ATP synthase and blocks proton flow through it. It does not act on the translocase, so A is wrong.

  3. (B) Atractyloside (and its relative carboxyatractyloside) binds ANT from the cytosolic side and locks it in the cytosol-facing conformation. This stops the exchange, so B is correct.

  4. (C) Amytal (amobarbital) is a barbiturate that inhibits Complex I (NADH dehydrogenase) and so blocks electron transfer. It does not act on the translocase, so C is wrong.

  5. (D) Bongkrekic acid binds ANT from the matrix side and locks it in the matrix-facing conformation. This also stops the exchange, so D is correct.

  6. The two ANT inhibitors are therefore atractyloside and bongkrekic acid, which is options B and D.

KEY IDEA

Atractyloside and bongkrekic acid both inhibit the adenine nucleotide translocase. They lock it in opposite conformations: atractyloside in the cytosol-facing one, bongkrekic acid in the matrix-facing one. Oligomycin blocks ATP synthase and amytal blocks Complex I.

WATCH OUT FOR

Treating every mitochondrial poison as a translocase inhibitor. Oligomycin (ATP synthase ) and amytal (Complex I) act on other components of oxidative phosphorylation, not on the ATP-ADP exchange.

From the GATE 2026 BT paper. Every question of this paper · Download the full paper · All 13 Metabolism questions, with notes

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