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1.
Bioinformatics ; 18(8): 1143-4, 2002 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-12176842

RESUMO

UNLABELLED: DiffTool is a resource to build and visualize protein clusters computed from a sequence database. The package provides a clustering tool to construct protein families according to sequence similarities and a web interface to query the corresponding clusters. A subtractive genome analysis tool selects protein families specific for a genome or a group of genomes. For each protein cluster, DiffTool includes access to sequences, coloured multiple alignments and phylogenetic trees. AVAILABILITY: A cluster database built from yeast and complete prokaryotic genomes is queryable at http://bioweb.pasteur.fr/seqanal/difftool. All the Perl sources are freely available to non-profit organizations upon request.


Assuntos
Análise por Conglomerados , Sistemas de Gerenciamento de Base de Dados , Bases de Dados de Proteínas , Armazenamento e Recuperação da Informação/métodos , Análise de Sequência de Proteína/métodos , Software , Gráficos por Computador , Genoma , Internet , Alinhamento de Sequência/métodos , Homologia de Sequência
2.
J Bacteriol ; 184(17): 4681-9, 2002 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-12169591

RESUMO

The way in which the genes involved in cysteine biosynthesis are regulated is poorly characterized in Bacillus subtilis. We showed that CysL (formerly YwfK), a LysR-type transcriptional regulator, activates the transcription of the cysJI operon, which encodes sulfite reductase. We demonstrated that a cysL mutant and a cysJI mutant have similar phenotypes. Both are unable to grow using sulfate or sulfite as the sulfur source. The level of expression of the cysJI operon is higher in the presence of sulfate, sulfite, or thiosulfate than in the presence of cysteine. Conversely, the transcription of the cysH and cysK genes is not regulated by these sulfur sources. In the presence of thiosulfate, the expression of the cysJI operon was reduced 11-fold, whereas the expression of the cysH and cysK genes was increased, in a cysL mutant. A cis-acting DNA sequence located upstream of the transcriptional start site of the cysJI operon (positions -76 to -70) was shown to be necessary for sulfur source- and CysL-dependent regulation. CysL also negatively regulates its own transcription, a common characteristic of the LysR-type regulators. Gel mobility shift assays and DNase I footprint experiments showed that the CysL protein specifically binds to cysJ and cysL promoter regions. This is the first report of a regulator of some of the genes involved in cysteine biosynthesis in B. subtilis.


Assuntos
Proteínas de Arabidopsis , Bacillus subtilis/genética , Óperon , Oxirredutases atuantes sobre Doadores de Grupo Enxofre/genética , Transativadores/fisiologia , Sequência de Aminoácidos , Bacillus subtilis/metabolismo , Sequência de Bases , Cisteína/biossíntese , Regulação Bacteriana da Expressão Gênica , Dados de Sequência Molecular , Regiões Promotoras Genéticas , Sulfito Redutase (Ferredoxina) , Enxofre/metabolismo , Transativadores/genética
3.
Microbiology (Reading) ; 147(Pt 10): 2643-2649, 2001 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-11577143

RESUMO

In silico subtractive/differential genome analysis is a powerful approach for identifying genus- or species-specific genes, or groups of genes that are responsible for a unique phenotype. By this method, one searches for genes present in one group of bacteria and absent in another group. A software package has been developed, named FindTarget, that has a user-friendly web interface to facilitate differential genome analysis. The user chooses the genomes to compare, the similarity criteria and the thresholds to decide if a gene has a counterpart in another genome. The searches are based on BLASTP comparisons of proteomes. FindTarget also includes access to sequences, coloured multiple alignments, phylogenetic trees of conserved proteins and links to public annotated databases which provide a means for validation of the results. To illustrate this approach, a FindTarget search for genes putatively involved in the specificity of cell envelope synthesis of Gram-negative bacteria is presented. The results show that most of the identified genes are clearly involved in cell wall processes, underlining the power of such an approach in general and that of FindTarget in particular.


Assuntos
Biologia Computacional , Genoma Bacteriano , Software , Proteínas de Bactérias/genética , Bactérias Gram-Negativas/genética , Bactérias Gram-Negativas/metabolismo , Proteoma , Interface Usuário-Computador
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