Plasmodium falciparum phosphoethanolamine methyltransferase is essential for malaria transmission.
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Nematode phospholipid metabolism: an example of closing the genome-structure-function circleGametocytocidal screen identifies novel chemical classes with Plasmodium falciparum transmission blocking activityPlasmodium falciparum CTP:phosphocholine cytidylyltransferase possesses two functional catalytic domains and is inhibited by a CDP-choline analog selected from a virtual screeningAn alternative mechanism for the methylation of phosphoethanolamine catalyzed by Plasmodium falciparum phosphoethanolamine methyltransferase.Structure, function and inhibition of the phosphoethanolamine methyltransferases of the human malaria parasites Plasmodium vivax and Plasmodium knowlesi.Characterization of Plasmodium phosphatidylserine decarboxylase expressed in yeast and application for inhibitor screeningProfiling the Essential Nature of Lipid Metabolism in Asexual Blood and Gametocyte Stages of Plasmodium falciparum.Apicoplast-Localized Lysophosphatidic Acid Precursor Assembly Is Required for Bulk Phospholipid Synthesis in Toxoplasma gondii and Relies on an Algal/Plant-Like Glycerol 3-Phosphate AcyltransferaseChanges in lipid composition during sexual development of the malaria parasite Plasmodium falciparum.In vitro anthelmintic efficacy of inhibitors of phosphoethanolamine Methyltransferases in Haemonchus contortusFrom crystal to compound: structure-based antimalarial drug discovery.New insight-guided approaches to detect, cure, prevent and eliminate malaria.Co-evolutionary analysis implies auxiliary functions of HSP110 in Plasmodium falciparum.Sex-Specific Biology of the Human Malaria Parasite Revealed from the Proteomes of Mature Male and Female Gametocytes.Lysophosphatidylcholine Regulates Sexual Stage Differentiation in the Human Malaria Parasite Plasmodium falciparum.The antimalarial activity of the pantothenamide α-PanAm is via inhibition of pantothenate phosphorylation.Less Lipid, More Commitment.A Novel Fluorescence Assay for Measuring Phosphatidylserine Decarboxylase Catalysis.Using Yeast Synthetic Lethality To Inform Drug Combination for Malaria.Realistically, how far are we from a universal malaria drug?Phosphoethanolamine-N-methyltransferase is a potential biomarker for the diagnosis of P. knowlesi and P. falciparum malaria.Lipid analysis of Eimeria sporozoites reveals exclusive phospholipids, a phylogenetic mosaic of endogenous synthesis, and a host-independent lifestyle.Probing sexual commitment at the single-cell levelIdentification of a putative methyltransferase gene of Babesia bigemina as a novel molecular biomarker uniquely expressed in parasite tick stages
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P2860
Plasmodium falciparum phosphoethanolamine methyltransferase is essential for malaria transmission.
description
article científic
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article scientifique
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articolo scientifico
@it
artigo científico
@pt
bilimsel makale
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scientific article published on 21 October 2013
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
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name
Plasmodium falciparum phosphoe ...... tial for malaria transmission.
@en
Plasmodium falciparum phosphoe ...... tial for malaria transmission.
@nl
type
label
Plasmodium falciparum phosphoe ...... tial for malaria transmission.
@en
Plasmodium falciparum phosphoe ...... tial for malaria transmission.
@nl
prefLabel
Plasmodium falciparum phosphoe ...... tial for malaria transmission.
@en
Plasmodium falciparum phosphoe ...... tial for malaria transmission.
@nl
P2093
P2860
P50
P921
P356
P1476
Plasmodium falciparum phosphoe ...... tial for malaria transmission.
@en
P2093
Albert Lee
Aprajita Garg
April M Bobenchik
Choukri Ben Mamoun
Dennis R Voelker
Jae-Yeon Choi
Laura Nic Lochlainn
Niseema Pachikara
Sophie H Adjalley
Swapna Samanta
P2860
P304
18262-18267
P356
10.1073/PNAS.1313965110
P407
P577
2013-10-21T00:00:00Z