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Heme detoxification is a biological process responsible for converting or neutralizing free heme, a pro-oxidant and cytotoxic molecule, commonly released during hemoglobin digestion. In malaria parasites such as Plasmodium falciparum, detoxification primarily proceeds via crystallization of heme into hemozoin, an inert polymer, within the digestive vacuole. Similar processes occur in other blood-feeding organisms and mammals, although strategies differ: mammals enzymatically degrade heme to bilirubin and excrete it, while some animals encapsulate heme in mineral particles to render it inert. Because efficient detoxification is essential for parasite survival, heme detoxification pathways and molecules involved (e.g., heme detoxification proteins, transporters like HrtBA) are targets for antimalarial drugs such as chloroquine and artemisinin, which act by disrupting this process. The process is not itself a druggable target in the conventional sense but refers to a set of biochemical strategies involving multiple molecular players. There is a fundamental issue with listing “heme detoxification” as a target molecule: it is a process, not a discrete, canonical target. Any attempt to obtain structured target-level data for “heme detoxification” will need to focus on specific molecular components such as “Heme detoxification protein (HDP)”, “HrtBA transporter”, or “heme crystallization pathway” for accurate data abstraction.
Inhibition of heme polymerization to hemozoin; Disruption of heme crystallization; Binding free heme to prevent toxicity
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