Expression and functional characterization of a Plasmodium falciparum Ca2+-ATPase (PfATP4) belonging to a subclass unique to apicomplexan organisms.
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non-SERCA-type Ca2+ -transporting P-ATPasenon-SERCA-type Ca2+ -transporting P-ATPase, putativenon-SERCA-type Ca2+ -transporting P-ATPase, putativenon-SERCA-type Ca2+ -transporting P-ATPase, putativenon-SERCA-type Ca2+ -transporting P-ATPase, putativenon-SERCA-type Ca2+ -transporting P-ATPase, putativenon-SERCA-type Ca2+ -transporting P-ATPase, putativenon-SERCA-type Ca2+ -transporting P-ATPase, putativenon-SERCA-type Ca2+ -transporting P-ATPase, putative
P1343
Expression in Yeast Links Field Polymorphisms in PfATP6 to in Vitro Artemisinin Resistance and Identifies New Inhibitor ClassesPurified E255L Mutant SERCA1a and Purified PfATP6 Are Sensitive to SERCA-type Inhibitors but Insensitive to ArtemisininsSpiroindolones, a potent compound class for the treatment of malariaThe 'permeome' of the malaria parasite: an overview of the membrane transport proteins of Plasmodium falciparum.The malaria parasite cation ATPase PfATP4 and its role in the mechanism of action of a new arsenal of antimalarial drugsUsing genetic methods to define the targets of compounds with antimalarial activityInterdomain communication in calcium pump as revealed in the crystal structures with transmembrane inhibitorsCyclopiazonic Acid Is Complexed to a Divalent Metal Ion When Bound to the Sarcoplasmic Reticulum Ca2+-ATPaseNa(+) regulation in the malaria parasite Plasmodium falciparum involves the cation ATPase PfATP4 and is a target of the spiroindolone antimalarialsThe Plasmodium berghei Ca(2+)/H(+) exchanger, PbCAX, is essential for tolerance to environmental Ca(2+) during sexual developmentNa+ Influx Induced by New Antimalarials Causes Rapid Alterations in the Cholesterol Content and Morphology of Plasmodium falciparumPyrazoleamide compounds are potent antimalarials that target Na+ homeostasis in intraerythrocytic Plasmodium falciparum.Diverse chemotypes disrupt ion homeostasis in the Malaria parasite.The digestive food vacuole of the malaria parasite is a dynamic intracellular Ca2+ store.Progressing the global antimalarial portfolio: finding drugs which target multiple Plasmodium life stages.Store depletion-induced calcium influx in rat cerebellar astrocytes.The Ca2+-ATPase (SERCA1) is inhibited by 4-aminoquinoline derivatives through interference with catalytic activation by Ca2+, whereas the ATPase E2 state remains functionalThe global pipeline of new medicines for the control and elimination of malariaHeterologous expression of plasmodial proteins for structural studies and functional annotation.Artemisinin induces doxorubicin resistance in human colon cancer cells via calcium-dependent activation of HIF-1alpha and P-glycoprotein overexpression.Malaria and iron: history and review.Membrane transport in the malaria parasite and its host erythrocyte.Calcium signalling in malaria parasites.Spiroindolone NITD609 is a novel antimalarial drug that targets the P-type ATPase PfATP4.Plasmodium falciparum apicoplast and its transcriptional regulation through calcium signaling.Signaling Strategies of Malaria Parasite for Its Survival, Proliferation, and Infection during Erythrocytic Stage.A yeast expression system for functional and pharmacological studies of the malaria parasite Ca²⁺/H⁺ antiporter.Ned-19 inhibition of parasite growth and multiplication suggests a role for NAADP mediated signalling in the asexual development of Plasmodium falciparum.Mechanism of antimalarial action of the synthetic trioxolane RBX11160 (OZ277).Comparative genomic and phylogenetic analyses of calcium ATPases and calcium-regulated proteins in the apicomplexa.P-type calcium ATPase functions as a core regulator of Beauveria bassiana growth, conidiation and responses to multiple stressful stimuli through cross-talk with signalling networks.Quantitative calcium measurements in subcellular compartments of Plasmodium falciparum-infected erythrocytes.Probing determinants of cyclopiazonic acid sensitivity of bacterial Ca2+-ATPases.Diverse antimalarials from whole-cell phenotypic screens disrupt malaria parasite ion and volume homeostasis.Biochemical characterization and chemical inhibition of PfATP4-associated Na-ATPase activity in membranesDevelopment of medicines for the control and elimination of malaria
P2860
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P1343
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P2860
Expression and functional characterization of a Plasmodium falciparum Ca2+-ATPase (PfATP4) belonging to a subclass unique to apicomplexan organisms.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
2001年论文
@zh
2001年论文
@zh-cn
name
Expression and functional char ...... que to apicomplexan organisms.
@en
Expression and functional characterization of a Plasmodium falciparum Ca2+-ATPase
@nl
type
label
Expression and functional char ...... que to apicomplexan organisms.
@en
Expression and functional characterization of a Plasmodium falciparum Ca2+-ATPase
@nl
prefLabel
Expression and functional char ...... que to apicomplexan organisms.
@en
Expression and functional characterization of a Plasmodium falciparum Ca2+-ATPase
@nl
P2093
P2860
P921
P356
P1476
Expression and functional char ...... que to apicomplexan organisms.
@en
P2093
P2860
P304
10782-10787
P356
10.1074/JBC.M010554200
P407
P577
2001-01-05T00:00:00Z