A secreted Plasmodium falciparum kinase reveals a signature motif for classification of tyrosine kinase-like kinases

被引:18
作者
Abdi, Abdirahman I. [1 ,2 ]
Carvalho, Teresa G. [3 ]
Wilkes, Jonathan M. [1 ]
Doerig, Christian [1 ,3 ]
机构
[1] Glasgow Biomed Res Ctr, Wellcome Trust Ctr Mol Parasitol, INSERM U609, Glasgow G12 8TA, Lanark, Scotland
[2] KEMRI Wellcome Trust Res Programme, Kilifi, Kenya
[3] Monash Univ, Dept Microbiol, Clayton, Vic 3800, Australia
来源
MICROBIOLOGY-SGM | 2013年 / 159卷
关键词
MIGRATION INHIBITORY FACTOR; IRAK-4; INHIBITORS; PROTEIN-KINASES; CRYSTAL-STRUCTURES; GENE FAMILY; RECEPTOR; IMMUNITY; HOMOLOG; ACTIVATION; KINOME;
D O I
10.1099/mic.0.070409-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Thorough bioinformatic and phylogenetic analyses of Plasmodium falciparum tyrosine kinase-like kinase (TKL) sequences revealed a clear evolutionary relationship of PF3D7_1121300 (thereafter called PfTKL2) to the IL-1 receptor-associated kinase (IRAK)/receptor-like kinase (RLK)/Pelle protein family. We identified a novel conserved motif that is unique to this family, as well as an insertion whose length allows distribution of its members into two distinct subfamilies, in a way that matches exactly the dichotomy between 'Tube/Tube-like kinases' (TTLKs) and 'Pelle-like kinases' (PLKs) distinguished previously on the basis of features in accessory domains. The PfTKL2 protein is expressed ubiquitously in asexual blood stages and in gametocytes, and the recombinant enzyme displays kinase activity in vitro. The protein is exported to the host erythrocyte; furthermore, in accordance with data from a previous study of the extracellular proteome of Plasmodium-infected erythrocytes, we show that PfTKL2 is secreted into the culture medium. Considering the functions of other members of the RLK/Pelle family in immunity, and its secretion to the extracellular medium, we speculate that PfTKL2 functions may include an immunomodulatory role promoting parasite survival in the human host.
引用
收藏
页码:2533 / 2547
页数:15
相关论文
共 57 条
[51]   Elevated Levels of the Plasmodium yoelii Homologue of Macrophage Migration Inhibitory Factor Attenuate Blood-Stage Malaria [J].
Thorat, Swati ;
Daly, Thomas M. ;
Bergman, Lawrence W. ;
Burns, James M., Jr. .
INFECTION AND IMMUNITY, 2010, 78 (12) :5151-5162
[52]   Localization of organellar proteins in Plasmodium falciparum using a novel set of transfection vectors and a new immunofluorescence fixation method [J].
Tonkin, CJ ;
van Dooren, GG ;
Spurck, TP ;
Struck, NS ;
Good, RT ;
Handman, E ;
Cowman, AF ;
McFadden, GI .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2004, 137 (01) :13-21
[53]   Tube Is an IRAK-4 Homolog in a Toll Pathway Adapted for Development and Immunity [J].
Towb, Par ;
Sun, Huaiyu ;
Wasserman, Steven A. .
JOURNAL OF INNATE IMMUNITY, 2009, 1 (04) :309-321
[54]   Crystal structures of IRAK-4 kinase in complex with inhibitors: A serine/threonine kinase with tyrosine as a gatekeeper [J].
Wang, Zhulun ;
Liu, Jinsong ;
Sudom, Athena ;
Ayres, Merrill ;
Li, Shyun ;
Wesche, Holger ;
Powers, Jay P. ;
Walker, Nigel P. C. .
STRUCTURE, 2006, 14 (12) :1835-1844
[55]   IRAK-4 Inhibitors for Inflammation [J].
Wang, Zhulun ;
Wesche, Holger ;
Stevens, Tracey ;
Walker, Nigel ;
Yeh, Wen-Chen .
CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2009, 9 (08) :724-737
[56]   Protein kinases of the human malaria parasite Plasmodium falciparum:: the kinome of a divergent eukaryote -: art. no. 79 [J].
Ward, P ;
Equinet, L ;
Packer, J ;
Doerig, C .
BMC GENOMICS, 2004, 5 (1)
[57]   The structural basis for activation of plant immunity by bacterial effector protein AvrPto [J].
Xing, Weiman ;
Zou, Yan ;
Liu, Qun ;
Liu, Jianing ;
Luo, Xi ;
Huang, Qingqiu ;
Chen, She ;
Zhu, Lihuang ;
Bi, Ruchang ;
Hao, Quan ;
Wu, Jia-Wei ;
Zhou, Jian-Min ;
Chai, Jijie .
NATURE, 2007, 449 (7159) :243-U11