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1.
Nucleic Acids Res ; 35(Database issue): D407-12, 2007 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-17142223

RESUMO

RegTransBase is a manually curated database of regulatory interactions in prokaryotes that captures the knowledge in public scientific literature using a controlled vocabulary. Although several databases describing interactions between regulatory proteins and their binding sites are already being maintained, they either focus mostly on the model organisms Escherichia coli and Bacillus subtilis or are entirely computationally derived. RegTransBase describes a large number of regulatory interactions reported in many organisms and contains the following types of experimental data: the activation or repression of transcription by an identified direct regulator, determining the transcriptional regulatory function of a protein (or RNA) directly binding to DNA (RNA), mapping or prediction of a binding site for a regulatory protein and characterization of regulatory mutations. Currently, RegTransBase content is derived from about 3000 relevant articles describing over 7000 experiments in relation to 128 microbes. It contains data on the regulation of about 7500 genes and evidence for 6500 interactions with 650 regulators. RegTransBase also contains manually created position weight matrices (PWM) that can be used to identify candidate regulatory sites in over 60 species. RegTransBase is available at http://regtransbase.lbl.gov.


Assuntos
Proteínas de Bactérias/metabolismo , Bases de Dados de Ácidos Nucleicos , Regulação Bacteriana da Expressão Gênica , Genoma Bacteriano , Elementos Reguladores de Transcrição , Fatores de Transcrição/metabolismo , Sítios de Ligação , Internet , Interface Usuário-Computador
2.
In Silico Biol ; 3(1-2): 3-15, 2003.
Artigo em Inglês | MEDLINE | ID: mdl-12762842

RESUMO

PhoH protein is a putative ATPase belonging to the phosphate regulon in Escherichia coli. EC-PhoH homologs are present in different organisms, but it is not clear if they are functionally related, besides nothing is known about their regulation. To distinguish true functional orthologs of EC-PhoH in different classes of bacteria and to identify their functional role in bacterial metabolic network we performed phylogenetic analysis of these proteins and comparative study of position and regulation of the related genes. Three groups of proteins were identified. Proteins of the first group (BS-PhoH orthologs) are present in most of bacteria and are proposed to be functionally linked to phospholipid metabolism and RNA modification. Proteins of the second group (BS-YlaK orthologs) are present in most of aerobes and Actinobacterial YlaK orthologs are shown to be members of a fatty acid beta-oxidation regulons. EC-PhoH orthologs are classified in a third group, specific for Enterobacteria. Functional role of PhoH homologs in the lipid and RNA metabolism and proposed interrelation of PhoH paralogs in one organism are discussed.


Assuntos
Bactérias/enzimologia , Bactérias/genética , Proteínas de Escherichia coli/classificação , Proteínas de Escherichia coli/genética , Genes Bacterianos/genética , Sequência de Bases , Biologia Computacional , Sequência Conservada , Regulação Bacteriana da Expressão Gênica , Regulação Enzimológica da Expressão Gênica , Genoma Bacteriano
3.
Genomics ; 82(6): 619-27, 2003 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-14611803

RESUMO

The biased distribution of dispersed repeat insertions in various types of primate specific alpha satellites (AS) is being discussed in the literature in relation to the modes of AS evolution and their possible roles in maintenance and disruption of functional centromeres. However, such a bias has not been properly documented on a genome-wide scale so far. In this work, using a representative sample of about 100 insertions we show that the "old" AS contains at least 10 times more dispersed repeats than the "new" one. In the new arrays insertions accumulate mostly in poorly homogenized areas, presumably in the edges, and in the old AS, throughout the whole array length. Dating of L1 insertions in the old AS revealed that their massive accumulation started at or after the time when the new AS emerged and expanded in the genome and the centromere function had shifted to the new AS arrays.


Assuntos
DNA Satélite/genética , Evolução Molecular , Sequências Repetitivas Dispersas/genética , Primatas/genética , Animais , Centrômero/genética , Bases de Dados de Ácidos Nucleicos , Humanos , Elementos Nucleotídeos Longos e Dispersos/genética , Fatores de Tempo
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