2W41

Crystal structure of Plasmodium falciparum glycerol kinase with ADP

2W41 の概要

• エントリーDOI: 10.2210/pdb2w41/pdb
• 関連するPDBエントリー: 2W40
• 分子名称: GLYCEROL KINASE, PUTATIVE, ADENOSINE-5'-DIPHOSPHATE, 1,2-ETHANEDIOL, ... (4 entities in total)
• 機能のキーワード: closed conformation, kinase, malaria, plasmodium, transferase, sugar kinase/hsp70/actin superfamily, glycerol kinase, open conformation
• 由来する生物種: PLASMODIUM FALCIPARUM
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 116828.63

構造登録者

Schnick, C.,Polley, S.D.,Fivelman, Q.L.,Ranford-Cartwright, L.,Wilkinson, S.R.,Brannigan, J.A.,Wilkinson, A.J.,Baker, D.A. (登録日: 2008-11-18, 公開日: 2008-12-02, 最終更新日: 2023-12-13)

主引用文献

Schnick, C.,Polley, S.D.,Fivelman, Q.L.,Ranford-Cartwright, L.,Wilkinson, S.R.,Brannigan, J.A.,Wilkinson, A.J.,Baker, D.A.
Structure and Non-Essential Function of Glycerol Kinase in Plasmodium Falciparum Blood Stages.
Mol.Microbiol., 71:533-, 2009

PubMed Abstract: Malaria pathology is caused by multiplication of asexual parasites within erythrocytes, whereas mosquito transmission of malaria is mediated by sexual precursor cells (gametocytes). Microarray analysis identified glycerol kinase (GK) as the second most highly upregulated gene in Plasmodium falciparum gametocytes with no expression detectable in asexual blood stage parasites. Phosphorylation of glycerol by GK is the rate-limiting step in glycerol utilization. Deletion of this gene from P. falciparum had no effect on asexual parasite growth, but surprisingly also had no effect on gametocyte development or exflagellation, suggesting that these life cycle stages do not utilize host-derived glycerol as a carbon source. Kinetic studies of purified PfGK showed that the enzyme is not regulated by fructose 1,6 bisphosphate. The high-resolution crystal structure of P. falciparum GK, the first of a eukaryotic GK, reveals two domains embracing a capacious ligand-binding groove. In the complexes of PfGK with glycerol and ADP, we observed closed and open forms of the active site respectively. The 27 degree domain opening is larger than in orthologous systems and exposes an extensive surface with potential for exploitation in selective inhibitor design should the enzyme prove to be essential in vivo either in the human or in the mosquito.

PubMed: 19040641
DOI: 10.1111/J.1365-2958.2008.06544.X

実験手法

X-RAY DIFFRACTION (2.41 Å)