Biochemical characterization ofPlasmodium falciparumCTP:phosphoethanolamine cytidylyltransferase shows that only one of the two cytidylyltransferase domains is active

Transport and pharmacodynamics of albitiazolium, an antimalarial drug candidate

(2012) S Wein et al.   BRITISH JOURNAL OF PHARMACOLOGY

The Kennedy pathway-De novo synthesis of phosphatidylethanolamine and phosphatidylcholine

(2010) Federica Gibellini et al.   IUBMB LIFE

The Kennedy phospholipid biosynthesis pathways are refractory to genetic disruption in Plasmodium berghei and therefore appear essential in blood stages

(2010) Sandrine Déchamps et al.   MOLECULAR AND BIOCHEMICAL PARASITOLOGY

MolProbity: all-atom structure validation for macromolecular crystallography

(2009) Vincent B. Chen et al.   ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY

Comparison of the cellular and biochemical properties ofPlasmodium falciparumcholine and ethanolamine kinases

(2009) Blandine Alberge et al.   BIOCHEMICAL JOURNAL

Crystal Structure of a Mammalian CTP: Phosphocholine Cytidylyltransferase Catalytic Domain Reveals Novel Active Site Residues within a Highly Conserved Nucleotidyltransferase Fold

(2009) Jaeyong Lee et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Rodent and nonrodent malaria parasites differ in their phospholipid metabolic pathways

(2009) Sandrine Déchamps et al.   JOURNAL OF LIPID RESEARCH

The ethanolamine branch of the Kennedy pathway is essential in the bloodstream form ofTrypanosoma brucei

(2009) Federica Gibellini et al.   MOLECULAR MICROBIOLOGY

The Homeostasis of Plasmodium falciparum-Infected Red Blood Cells

(2009) Jakob M. A. Mauritz et al.   PLoS Computational Biology

PlasmoDB: a functional genomic database for malaria parasites

(2008) C. Aurrecoechea et al.   NUCLEIC ACIDS RESEARCH