LeishCyc: a biochemical pathways database for Leishmania major

被引:50
作者
Doyle, Maria A. [1 ,2 ]
MacRae, James I. [1 ,2 ]
De Souza, David P. [1 ,2 ]
Saunders, Eleanor C. [1 ,2 ]
McConville, Malcolm J. [1 ,2 ]
Likic, Vladimir A. [1 ,2 ]
机构
[1] Univ Melbourne, Dept Biochem & Mol Biol, Parkville, Vic 3010, Australia
[2] Univ Melbourne, Mol Sci & Biotechnol Inst Bio21, Parkville, Vic 3010, Australia
基金
澳大利亚国家健康与医学研究理事会; 澳大利亚研究理事会;
关键词
COMPARATIVE GENOMICS; METABOLISM; VIRULENCE; PARASITE; SYNTHASE; METACYC; DISEASE; TOOLS; GENE;
D O I
10.1186/1752-0509-3-57
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Leishmania spp. are sandfly transmitted protozoan parasites that cause a spectrum of diseases in more than 12 million people worldwide. Much research is now focusing on how these parasites adapt to the distinct nutrient environments they encounter in the digestive tract of the sandfly vector and the phagolysosome compartment of mammalian macrophages. While data mining and annotation of the genomes of three Leishmania species has provided an initial inventory of predicted metabolic components and associated pathways, resources for integrating this information into metabolic networks and incorporating data from transcript, protein, and metabolite profiling studies is currently lacking. The development of a reliable, expertly curated, and widely available model of Leishmania metabolic networks is required to facilitate systems analysis, as well as discovery and prioritization of new drug targets for this important human pathogen. Description: The LeishCyc database was initially built from the genome sequence of Leishmania major (v5.2), based on the annotation published by the Wellcome Trust Sanger Institute. LeishCyc was manually curated to remove errors, correct automated predictions, and add information from the literature. The ongoing curation is based on public sources, literature searches, and our own experimental and bioinformatics studies. In a number of instances we have improved on the original genome annotation, and, in some ambiguous cases, collected relevant information from the literature in order to help clarify gene or protein annotation in the future. All genes in LeishCyc are linked to the corresponding entry in GeneDB (Wellcome Trust Sanger Institute). Conclusion: The LeishCyc database describes Leishmania major genes, gene products, metabolites, their relationships and biochemical organization into metabolic pathways. LeishCyc provides a systematic approach to organizing the evolving information about Leishmania biochemical networks and is a tool for analysis, interpretation, and visualization of Leishmania Omics data (transcriptomics, proteomics, metabolomics) in the context of metabolic pathways. LeishCyc is the first such database for the Trypanosomatidae family, which includes a number of other important human parasites. Flexible query/visualization capabilities are provided by the Pathway Tools software and its Web interface. The LeishCyc database is made freely available over the Internet http://www.leishcyc.org.
引用
收藏
页数:12
相关论文
共 53 条
[1]   Genomic-scale prioritization of drug targets: the TDR Targets database [J].
Agueero, Fernan ;
Al-Lazikani, Bissan ;
Aslett, Martin ;
Berriman, Matthew ;
Buckner, Frederick S. ;
Campbell, Robert K. ;
Carmona, Santiago ;
Carruthers, Ian M. ;
Chan, A. W. Edith ;
Chen, Feng ;
Crowther, Gregory J. ;
Doyle, Maria A. ;
Hertz-Fowler, Christiane ;
Hopkins, Andrew L. ;
McAllister, Gregg ;
Nwaka, Solomon ;
Overington, John P. ;
Pain, Arnab ;
Paolini, Gala V. ;
Pieper, Ursula ;
Ralph, Stuart A. ;
Riechers, Aaron ;
Roos, David S. ;
Sali, Andrej ;
Shanmugam, Dhanasekaran ;
Suzuki, Takashi ;
Van Voorhis, Wesley C. ;
Verlinde, Christophe L. M. J. .
NATURE REVIEWS DRUG DISCOVERY, 2008, 7 (11) :900-907
[2]   Integration of tools and resources for display and analysis of genomic data for protozoan parasites [J].
Aslett, M ;
Mooney, P ;
Adlem, E ;
Berriman, M ;
Berry, A ;
Hertz-Fowler, C ;
Ivens, AC ;
Kerhornou, A ;
Parkhill, J ;
Peacock, CS ;
Wood, V ;
Rajandream, MA ;
Bartell, B ;
Tivey, A .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 2005, 35 (05) :481-493
[3]   Mitochondrial glutamate dehydrogenase from Leishmania tarentolae is a guide RNA-binding protein [J].
Bringaud, F ;
Stripecke, R ;
Frech, GC ;
Freedland, S ;
Turck, C ;
Byrne, EM ;
Simpson, L .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (07) :3915-3923
[4]  
Caspi R, 2008, NUCLEIC ACIDS RES, V36, pD623, DOI [10.1093/nar/gkm900, 10.1093/nar/gkt1103]
[5]   Systems analysis of metabolism in the pathogenic trypanosomatid Leishmania major [J].
Chavali, Arvind K. ;
Whittemore, Jeffrey D. ;
Eddy, James A. ;
Williams, Kyle T. ;
Papin, Jason A. .
MOLECULAR SYSTEMS BIOLOGY, 2008, 4 (1) :177
[6]  
CHUKUALIM B, 2008, 4 INT SOC COMP B S10, V9, P5
[7]   Global gene expression in Leishmania [J].
Cohen-Freue, Gabriela ;
Holzer, Timothy R. ;
Forney, James D. ;
McMaster, W. Robert .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 2007, 37 (10) :1077-1086
[8]   Drug resistance in leishmaniasis [J].
Croft, SL ;
Sundar, S ;
Fairlamb, AH .
CLINICAL MICROBIOLOGY REVIEWS, 2006, 19 (01) :111-+
[9]   Progressive peak clustering in GC-MS metabolomic experiments applied to Leishmania parasites [J].
De Souza, David P. ;
Saunders, Eleanor C. ;
McConville, Malcolm J. ;
Likic, Vladimir A. .
BIOINFORMATICS, 2006, 22 (11) :1391-1396
[10]   The protozoan inositol phosphorylceramide synthase - A novel drug target that defines a new class of sphingolipid synthase [J].
Denny, Paul W. ;
Shams-Eldin, Hosam ;
Price, Helen. P. ;
Smith, Deborah F. ;
Schwarz, Ralph T. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (38) :28200-28209