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To survive and replicate during the intraerythrocytic lifecycle stages, the malaria parasite uses a range of transport processes to take up nutrients, export waste products, and maintain tight regulation over its own internal ionic environment [1]. Plasmodium membrane transport proteins are candidate targets for antimalarial drug discovery but have also been shown to play a role in the development of drug resistance.
PfATP4 (Plasmodium falciparum non-SERCA-type Ca2+ -transporting P-ATPase) C Show summary » More detailed page |
Plasmodium falciparum V-type proton ATPase subunit D C Show summary » More detailed page |
PfCARL (Plasmodium falciparum cyclic amine resistance locus protein) C Show summary » More detailed page |
PfHT1 (Plasmodium falciparum hexose transporter) C Show summary » More detailed page |
PfNCR1 (Plasmodium falciparum Niemann-Pick type C1-related protein) C Show summary » More detailed page |
Database page citation:
Transporters (Plasmodium spp.). Accessed on 15/10/2024. IUPHAR/BPS Guide to PHARMACOLOGY, http://www.guidetopharmacology.org/GRAC/FamilyDisplayForward?familyId=1064.
Concise Guide to PHARMACOLOGY citation:
Alexander SPH, Kelly E, Mathie AA, Peters JA, Veale EL, Armstrong JF, Buneman OP, Faccenda E, Harding SD, Spedding M, Cidlowski JA, Fabbro D, Davenport AP, Striessnig J, Davies JA et al. (2023) The Concise Guide to PHARMACOLOGY 2023/24: Introduction and Other Protein Targets. Br J Pharmacol. 180 Suppl 2:S1-22.