2VWA

Crystal structure of a sporozoite protein essential for liver stage development of malaria parasite

2VWA の概要

• エントリーDOI: 10.2210/pdb2vwa/pdb
• 分子名称: PUTATIVE UNCHARACTERIZED PROTEIN PF13_0012, PHOSPHATIDYLETHANOLAMINE (3 entities in total)
• 機能のキーワード: unknown function
• 由来する生物種: PLASMODIUM FALCIPARUM (MALARIA PARASITE)
• タンパク質・核酸の鎖数: 6
• 化学式量合計: 77780.00

構造登録者

Sharma, A.,Sharma, A.,Yogavel, M.,Gill, J.,Akhouri, R.R. (登録日: 2008-06-20, 公開日: 2008-07-08, 最終更新日: 2024-11-20)

主引用文献

Sharma, A.,Yogavel, M.,Akhouri, R.R.,Gill, J.,Sharma, A.
Crystal Structure of Soluble Domain of Malaria Sporozoite Protein Uis3 in Complex with Lipid.
J.Biol.Chem., 283:24077-, 2008

PubMed Abstract: Malaria parasite UIS3 (up-regulated in infective sporozoites gene 3) is essential for sporozoite development in infected hepatocytes. UIS3 encodes for a membrane protein that is localized to the parasite parasitophorous vacuolar membrane in infected hepatocytes. We describe here 2.5-A resolution crystal structure of Plasmodium falciparum UIS3 soluble domain (PfUIS3(130-229)) in complex with the lipid phosphatidylethanolamine (PE). PfUIS3(130-229) is a novel, compact, and all alpha-helical structure bound to one molecule of PE. The PfUIS3(130-229)-PE complex structure reveals a novel binding site with specific interactions between PfUIS3(130-229) and the PE head group. One acyl chain of PE wraps around part of PfUIS3(130-229) and docks onto a hydrophobic channel. We additionally provide new structural and biochemical evidence of PfUIS3(130-229) interactions with lipids (phosphatidylethanolamine), with phospholipid liposomes, and with the human liver fatty acid-binding protein. The direct interaction of PfUIS3(130-229) with liver fatty acid-binding protein most likely provides the parasite with a conduit for importing essential fatty acids/lipids. Therefore, our analyses have implications for lipid transport into the parasite during the rapid growth phases of sporozoites. Given that PfUIS3 is essential for establishment of liver stage infection by P. falciparum, our data provide a new target for abrogating parasite development within liver cells before typical symptoms of malaria can manifest.

PubMed: 18577521
DOI: 10.1074/JBC.M801946200

実験手法

X-RAY DIFFRACTION (2.5 Å)