A novel heteromeric pantothenate kinase complex in apicomplexan parasites

• Published in: PLoS pathogens Vol. 17; no. 7; p. e1009797
• Main Authors: Tjhin, Erick T, Howieson, Vanessa M, Spry, Christina, van Dooren, Giel G, Saliba, Kevin J
• Format: Journal Article
• Language: English
• Published: San Francisco Public Library of Science 29.07.2021; Public Library of Science (PLoS)
• Subjects: Analysis; Biology and Life Sciences; Chemical properties; Coenzyme A; Coenzymes; Enzyme kinetics; Experiments; Genomes; Homology; Kinases; Medicine and Health Sciences; Mutation; Organisms; Pantothenate kinase; Parasites; Peptides; Phosphorylation; Plasmodium falciparum; Proteins; Research and Analysis Methods; Toxoplasma; Australia
• ISSN: 1553-7374; 1553-7366; 1553-7374
• DOI: 10.1371/journal.ppat.1009797

Coenzyme A is synthesised from pantothenate via five enzyme-mediated steps. The first step is catalysed by pantothenate kinase (PanK). All PanKs characterised to date form homodimers. Many organisms express multiple PanKs. In some cases, these PanKs are not functionally redundant, and some appear to be non-functional. Here, we investigate the PanKs in two pathogenic apicomplexan parasites, Plasmodium falciparum and Toxoplasma gondii. Each of these organisms express two PanK homologues (PanK1 and PanK2). We demonstrate that PfPanK1 and PfPanK2 associate, forming a single, functional PanK complex that includes the multi-functional protein, Pf14-3-3I. Similarly, we demonstrate that TgPanK1 and TgPanK2 form a single complex that possesses PanK activity. Both TgPanK1 and TgPanK2 are essential for T. gondii proliferation, specifically due to their PanK activity. Our study constitutes the first examples of heteromeric PanK complexes in nature and provides an explanation for the presence of multiple PanKs within certain organisms.