Expansion of the BioCyc collection of pathway/genome databases to 160 genomes

被引:415
作者
Karp, PD
Ouzounis, CA
Moore-Kochlacs, C
Goldovsky, L
Kaipa, P
Ahrén, D
Tsoka, S
Darzentas, N
Kunin, V
López-Bigas, N
机构
[1] SRI Int, Bioinformat Res Grp, Menlo Pk, CA 94025 USA
[2] EMBL Cambridge Outstn, European Bioinformat Inst, Computat Genom Grp, Cambridge CB10 1SD, England
关键词
D O I
10.1093/nar/gki892
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The BioCyc database collection is a set of 160 pathway/genome databases (PGDBs) for most eukaryotic and prokaryotic species whose genomes have been completely sequenced to date. Each PGDB in the BioCyc collection describes the genome and predicted metabolic network of a single organism, inferred from the MetaCyc database, which is a reference source on metabolic pathways from multiple organisms. In addition, each bacterial PGDB includes predicted operons for the corresponding species. The BioCyc collection provides a unique resource for computational systems biology, namely global and comparative analyses of genomes and metabolic networks, and a supplement to the BioCyc resource of curated PGDBs. The Omics viewer available through the BioCyc website allows scientists to visualize combinations of gene expression, proteomics and metabolomics data on the metabolic maps of these organisms. This paper discusses the computational methodology by which the BioCyc collection has been expanded, and presents an aggregate analysis of the collection that includes the range of number of pathways present in these organisms, and the most frequently observed pathways. We seek scientists to adopt and curate individual PGDBs within the BioCyc collection. Only by harnessing the expertise of many scientists we can hope to produce biological databases, which accurately reflect the depth and breadth of knowledge that the biomedical research community is producing.
引用
收藏
页码:6083 / 6089
页数:7
相关论文
共 39 条
[21]   MetaCyc: a multiorganism database of metabolic pathways and enzymes [J].
Krieger, CJ ;
Zhang, PF ;
Mueller, LA ;
Wang, A ;
Paley, S ;
Arnaud, M ;
Pick, J ;
Rhee, SY ;
Karp, PD .
NUCLEIC ACIDS RESEARCH, 2004, 32 :D438-D442
[22]   Querying and computing with BioCyc databases [J].
Krummenacker, M ;
Paley, S ;
Mueller, L ;
Yan, T ;
Karp, PD .
BIOINFORMATICS, 2005, 21 (16) :3454-3455
[23]   The complete genome sequence of Francisella tularensis, the causative agent of tularemia [J].
Larsson, P ;
Oyston, PCF ;
Chain, P ;
Chu, MC ;
Duffield, M ;
Fuxelius, HH ;
Garcia, E ;
Hälltorp, G ;
Johansson, D ;
Isherwood, KE ;
Karp, PD ;
Larsson, E ;
Liu, Y ;
Michell, S ;
Prior, J ;
Prior, R ;
Malfatti, S ;
Sjöstedt, A ;
Svensson, K ;
Thompson, N ;
Vergez, L ;
Wagg, JK ;
Wren, BW ;
Lindler, LE ;
Andersson, SGE ;
Forsman, M ;
Titball, RW .
NATURE GENETICS, 2005, 37 (02) :153-159
[24]   Global properties of the metabolic map of Escherichia coli [J].
Ouzounis, CA ;
Karp, PD .
GENOME RESEARCH, 2000, 10 (04) :568-576
[25]  
Ouzounis CA, 2002, GENOME BIOL, V3
[26]   WIT: integrated system for high-throughput genome sequence analysis and metabolic reconstruction [J].
Overbeek, R ;
Larsen, N ;
Pusch, GD ;
D'Souza, M ;
Selkov, E ;
Kyrpides, N ;
Fonstein, M ;
Maltsev, N ;
Selkov, E .
NUCLEIC ACIDS RESEARCH, 2000, 28 (01) :123-125
[27]   Evaluation of computational metabolic-pathway predictions for Helicobacter pylori [J].
Paley, SM ;
Karp, PD .
BIOINFORMATICS, 2002, 18 (05) :715-724
[28]   The phylogenetic extent of metabolic enzymes and pathways [J].
Peregrin-Alvarez, JM ;
Tsoka, S ;
Ouzounis, CA .
GENOME RESEARCH, 2003, 13 (03) :422-427
[29]   The Comprehensive Microbial Resource [J].
Peterson, JD ;
Umayam, LA ;
Dickinson, T ;
Hickey, EK ;
White, O .
NUCLEIC ACIDS RESEARCH, 2001, 29 (01) :123-125
[30]   NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins [J].
Pruitt, KD ;
Tatusova, T ;
Maglott, DR .
NUCLEIC ACIDS RESEARCH, 2005, 33 :D501-D504