iCR: a web tool to identify conserved targets of a regulatory protein across the multiple related prokaryotic species

被引:4
|
作者
Ranjan, Sarita [1 ]
Seshadri, Jayshree [1 ]
Vindal, Vaibhav [1 ]
Yellaboina, Sailu [1 ]
Ranjan, Akash [1 ]
机构
[1] EMBnet India Node, Computat & Funct Genom Grp, Sun Ctr Excellence Med Bioinformat, Ctr DNA Fingerprinting & Diagnost, Hyderabad 500076, Andhra Pradesh, India
关键词
D O I
10.1093/nar/gkl202
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
Gene regulatory circuits are often commonly shared between two closely related organisms. Our web tool iCR (identify Conserved target of a Regulon) makes use of this fact and identify conserved targets of a regulatory protein. iCR is a special refined extension of our previous tool PredictRegulon - that predicts genome wide, the potential binding sites and target operons of a regulatory protein in a single user selected genome. Like PredictRegulon, the iCR accepts known binding sites of a regulatory protein as ungapped multiple sequence alignment and provides the potential binding sites. However important differences are that the user can select more than one genome at a time and the output reports the genes that are common in two or more species. In order to achieve this, iCR makes use of Cluster of Orthologous Group (COG) indices for the genes. This tool analyses the upstream region of all user-selected prokaryote genome and gives the output based on conservation target orthologs. iCR also reports the Functional class codes based on COG classification for the encoded proteins of downstream genes which helps user understand the nature of the co- regulated genes at the result page itself. iCR is freely accessible at http://www.cdfd.org.in/icr/.
引用
收藏
页码:W584 / W587
页数:4
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