The Princeton Protein Orthology Database (P-POD): A Comparative Genomics Analysis Tool for Biologists

被引:64
作者
Heinicke, Sven [1 ]
Livstone, Michael S. [1 ]
Lu, Charles [1 ]
Oughtred, Rose [1 ]
Kang, Fan [1 ]
Angiuoli, Samuel V. [2 ,3 ]
White, Owen [2 ]
Botstein, David [1 ]
Dolinski, Kara [1 ]
机构
[1] Princeton Univ, Lewis Sigler Inst Integrat Genom, Princeton, NJ 08544 USA
[2] Inst Genom Res, Rockville, MD USA
[3] Univ Maryland, Ctr Bioinformat & Computat Biol, College Pk, MD 20742 USA
来源
PLOS ONE | 2007年 / 2卷 / 08期
关键词
D O I
10.1371/journal.pone.0000766
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Many biological databases that provide comparative genomics information and tools are now available on the internet. While certainly quite useful, to our knowledge none of the existing databases combine results from multiple comparative genomics methods with manually curated information from the literature. Here we describe the Princeton Protein Orthology Database (P-POD, http://ortholog.princeton.edu), a user-friendly database system that allows users to find and visualize the phylogenetic relationships among predicted orthologs (based on the OrthoMCL method) to a query gene from any of eight eukaryotic organisms, and to see the orthologs in a wider evolutionary context (based on the Jaccard clustering method). In addition to the phylogenetic information, the database contains experimental results manually collected from the literature that can be compared to the computational analyses, as well as links to relevant human disease and gene information via the OMIM, model organism, and sequence databases. Our aim is for the P-POD resource to be extremely useful to typical experimental biologists wanting to learn more about the evolutionary context of their favorite genes. P-POD is based on the commonly used Generic Model Organism Database (GMOD) schema and can be downloaded in its entirety for installation on one's own system. Thus, bioinformaticians and software developers may also find P-POD useful because they can use the P-POD database infrastructure when developing their own comparative genomics resources and database tools.
引用
收藏
页数:15
相关论文
共 115 条
[31]   Mutations in the Δ1-pyrroline 5-carboxylate dehydrogenase gene cause type II hyperprolinemia [J].
Geraghty, MT ;
Vaughn, D ;
Nicholson, AJ ;
Lin, WW ;
Jimenez-Sanchez, G ;
Obie, C ;
Flynn, MP ;
Valle, D ;
Hu, CAA .
HUMAN MOLECULAR GENETICS, 1998, 7 (09) :1411-1415
[32]   Glycosylphosphatidylinositol anchors represent the major carbohydrate modification in proteins of intraerythrocytic stage Plasmodium falciparum [J].
Gowda, DC ;
Gupta, P ;
Davidson, EA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (10) :6428-6439
[33]   ALG12 mannosyltransferase defect in congenital disorder of glycosylation type Ig [J].
Grubenmann, CE ;
Frank, CG ;
Kjaergaard, S ;
Berger, EG ;
Aebi, M ;
Hennet, T .
HUMAN MOLECULAR GENETICS, 2002, 11 (19) :2331-2339
[34]   LETHALITY IN YEAST OF TRICHOTHIODYSTROPHY (TTD) MUTATIONS IN THE HUMAN XERODERMA-PIGMENTOSUM GROUP-D GENE - IMPLICATIONS FOR TRANSCRIPTIONAL DEFECT IN TTD [J].
GUZDER, SN ;
SUNG, P ;
PRAKASH, S ;
PRAKASH, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (30) :17660-17663
[35]   EXPRESSION OF HETEROLOGOUS PHOSPHOFRUCTOKINASE GENES IN YEAST [J].
HEINISCH, JJ .
FEBS LETTERS, 1993, 328 (1-2) :35-40
[36]   RNA polymerase IV directs silencing of endogenous DNA [J].
Herr, AJ ;
Jensen, MB ;
Dalmay, T ;
Baulcombe, DC .
SCIENCE, 2005, 308 (5718) :118-120
[37]   The C66W mutation in the deafness dystonia peptide 1 (DDP1) affects the formation of functional DDP1•TIM13 complexes in the mitochondrial intermembrane space [J].
Hofmann, S ;
Rothbauer, U ;
Mühlenbein, N ;
Neupert, W ;
Gerbitz, KD ;
Brunner, M ;
Bauer, MF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (26) :23287-23293
[38]   Functional assessment of the carboxy-terminus of the Wilson disease copper-transporting ATPase, ATP7B [J].
Hsi, G ;
Cullen, LM ;
Glerum, DM ;
Cox, DW .
GENOMICS, 2004, 83 (03) :473-481
[39]   Cloning, characterization, and expression of cDNAs encoding human Delta(1)-pyrroline-5-carboxylate dehydrogenase [J].
Hu, CA ;
Lin, WW ;
Valle, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (16) :9795-9800
[40]   SEM1, a homologue of the split hand split foot malformation candidate gene Dss1, regulates exocytosis and pseudohyphal differentiation in yeast [J].
Jäntti, J ;
Lahdenranta, J ;
Olkkonen, VM ;
Söderlund, H ;
Keränen, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (03) :909-914