Sickling of RBC in sickle-cell anemia is due to polymerization of
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The enzyme defect in acute intermittent porphyria
Uroporphyrinogen synthase I
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The compound that facilitates the release of O2 from oxyhemoglobin
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Name the compound that is increased in RBC of anemic patients to facilitate the supply of O2 to the tissues
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The disorders characterized by decreased synthesis or total absence of globin chains of hemoglobin are collectively known as
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RNA molecules that act as enzymes
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Name the amino acid that directly participates in the synthesis of heme
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The characteristic red colour of hemoglobin is due to
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The extrinsic and intrinsic pathways result in the formation of a common activated factor
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