The product formed when heme oxygenase cleaves heme
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Sickling of RBC in sickle-cell anemia is due to polymerization of
Deoxyhemoglobin,
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The oxidation of ferrous (Fe2+) iron to ferric (Fe3+) iron in hemoglobin results in the formation of a compound namely
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A non-protein amino acid
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The patients of sickle-cell anemia are resistant to
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The characteristic red colour of hemoglobin is due to
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The number of ATP produced when a molecule of acetyl CoA is oxidized through citric acid cycle
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The enzyme that catalyses the formation of carbonic acid
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The intermediate of citric acid cycle that is involved in heme synthesis
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