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Registro Completo |
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Biblioteca(s): |
Embrapa Agricultura Digital. |
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Data corrente: |
02/12/2010 |
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Data da última atualização: |
27/01/2020 |
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Tipo da produção científica: |
Resumo em Anais de Congresso |
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Autoria: |
ALVAREZ, J. C.; HERAI, R. H.; CARAZZOLLE, M. F.; PEREIRA, G. G. A. |
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Afiliação: |
UNICAMP; UNICAMP, CNPTIA; UNICAMP; UNICAMP. |
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Título: |
PredIP: an in silico approach for automated protein interaction prediction in genomic and transcriptomic sequence databanks. |
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Ano de publicação: |
2010 |
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Fonte/Imprenta: |
In: INTERNATIONAL CONFERENCE OF THE BRAZILIAN ASSOCIATION FOR BIOINFORMATICS AND COMPUTATIONAL BIOLOGY, 6., 2010, Ouro Preto. Abstracts... [S.l.: s.n.], 2010. |
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Páginas: |
p. 85. |
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Idioma: |
Inglês |
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Notas: |
X-meeting 2010. |
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Conteúdo: |
The fast-growing amount of protein interaction databanks have made possible to analyze deeply several metabolic or signaling pathways in different organisms. The information available in such databanks can be used to predict new protein interactions in transcriptome or proteome sequences, most of times this task is done by sequence homology or by structure similarity. In this way, several in silico systems were already proposed, like Peimap, which makes its predictions based on experimentally validated protein-protein interaction databanks of different organisms. A restricting criteria to use such tools is the input data, that only accepts proteomic sequences. Based on the importance of the protein complex prediction, and in the fact that several genomes still do not have a transcriptome or an annotated proteome, we propose an integrative Web-based system that can perform, automatically, protein-protein interaction predictions considering also genomic sequences. Our prediction approach was organized in two steps. In the first, a system analyses the input dataset and uses FrameDP and Augustus, two free softwares, to predict proteins. In the second step, the predicted proteins are aligned against avaiable databases (DIP, Mint, BioGrid, Bind, HPRD, StringInts, IntAct) of protein-protein interactions using psi-blast software. Finally, the aligned sequences are analyzed by our pipeline, called PredIP, that creates an interactive chart representing all relationships between each protein and its respective interactor. Our in silico strategy to predict pairs of protein complexes can be applied in genomic, transcriptomic or proteomic data, is not necessary knowing previously the transcriptome or proteome of a considered organism. PredIP has already been tested to predict protein interactions between proteins of Moliniopthora perniciosa fungus genome. Hundreds of possible protein complex have been predicted, and have already been described in the literature as possible. The PredIP system structure can be incrementally updated with new discovered protein-protein interactions to perform new predictions. Predicted protein complex in M. perniciosa has already been proved to exist, and new predicted complex will be experimentally validated by our group, enabling a better understands of relationship between the fungus proteins. Furthermore, PredIP can be a useful tool to predict interactions between two distinct organisms. As described in specialized literature, PredIP is the first automated pipeline to predict protein complexes from genomic or transcriptomic sequences. MenosThe fast-growing amount of protein interaction databanks have made possible to analyze deeply several metabolic or signaling pathways in different organisms. The information available in such databanks can be used to predict new protein interactions in transcriptome or proteome sequences, most of times this task is done by sequence homology or by structure similarity. In this way, several in silico systems were already proposed, like Peimap, which makes its predictions based on experimentally validated protein-protein interaction databanks of different organisms. A restricting criteria to use such tools is the input data, that only accepts proteomic sequences. Based on the importance of the protein complex prediction, and in the fact that several genomes still do not have a transcriptome or an annotated proteome, we propose an integrative Web-based system that can perform, automatically, protein-protein interaction predictions considering also genomic sequences. Our prediction approach was organized in two steps. In the first, a system analyses the input dataset and uses FrameDP and Augustus, two free softwares, to predict proteins. In the second step, the predicted proteins are aligned against avaiable databases (DIP, Mint, BioGrid, Bind, HPRD, StringInts, IntAct) of protein-protein interactions using psi-blast software. Finally, the aligned sequences are analyzed by our pipeline, called PredIP, that creates an interactive chart representing all relationships between each p... Mostrar Tudo |
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Palavras-Chave: |
Bases de dados; Interação entre proteínas; Proteínas. |
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Thesaurus Nal: |
Databases; Moniliophthora perniciosa; Proteins. |
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Categoria do assunto: |
-- |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/23818/1/p85.pdf
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Marc: |
LEADER 03456nam a2200241 a 4500
001 1868512
005 2020-01-27
008 2010 bl uuuu u00u1 u #d
100 1 $aALVAREZ, J. C.
245 $aPredIP$ban in silico approach for automated protein interaction prediction in genomic and transcriptomic sequence databanks.$h[electronic resource]
260 $aIn: INTERNATIONAL CONFERENCE OF THE BRAZILIAN ASSOCIATION FOR BIOINFORMATICS AND COMPUTATIONAL BIOLOGY, 6., 2010, Ouro Preto. Abstracts... [S.l.: s.n.]$c2010
300 $ap. 85.
500 $aX-meeting 2010.
520 $aThe fast-growing amount of protein interaction databanks have made possible to analyze deeply several metabolic or signaling pathways in different organisms. The information available in such databanks can be used to predict new protein interactions in transcriptome or proteome sequences, most of times this task is done by sequence homology or by structure similarity. In this way, several in silico systems were already proposed, like Peimap, which makes its predictions based on experimentally validated protein-protein interaction databanks of different organisms. A restricting criteria to use such tools is the input data, that only accepts proteomic sequences. Based on the importance of the protein complex prediction, and in the fact that several genomes still do not have a transcriptome or an annotated proteome, we propose an integrative Web-based system that can perform, automatically, protein-protein interaction predictions considering also genomic sequences. Our prediction approach was organized in two steps. In the first, a system analyses the input dataset and uses FrameDP and Augustus, two free softwares, to predict proteins. In the second step, the predicted proteins are aligned against avaiable databases (DIP, Mint, BioGrid, Bind, HPRD, StringInts, IntAct) of protein-protein interactions using psi-blast software. Finally, the aligned sequences are analyzed by our pipeline, called PredIP, that creates an interactive chart representing all relationships between each protein and its respective interactor. Our in silico strategy to predict pairs of protein complexes can be applied in genomic, transcriptomic or proteomic data, is not necessary knowing previously the transcriptome or proteome of a considered organism. PredIP has already been tested to predict protein interactions between proteins of Moliniopthora perniciosa fungus genome. Hundreds of possible protein complex have been predicted, and have already been described in the literature as possible. The PredIP system structure can be incrementally updated with new discovered protein-protein interactions to perform new predictions. Predicted protein complex in M. perniciosa has already been proved to exist, and new predicted complex will be experimentally validated by our group, enabling a better understands of relationship between the fungus proteins. Furthermore, PredIP can be a useful tool to predict interactions between two distinct organisms. As described in specialized literature, PredIP is the first automated pipeline to predict protein complexes from genomic or transcriptomic sequences.
650 $aDatabases
650 $aMoniliophthora perniciosa
650 $aProteins
653 $aBases de dados
653 $aInteração entre proteínas
653 $aProteínas
700 1 $aHERAI, R. H.
700 1 $aCARAZZOLLE, M. F.
700 1 $aPEREIRA, G. G. A.
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Registro original: |
Embrapa Agricultura Digital (CNPTIA) |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Instrumentação. Para informações adicionais entre em contato com cnpdia.biblioteca@embrapa.br. |
Registro Completo
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Biblioteca(s): |
Embrapa Instrumentação. |
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Data corrente: |
14/12/2007 |
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Data da última atualização: |
08/01/2008 |
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Tipo da produção científica: |
Resumo em Anais de Congresso |
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Circulação/Nível: |
-- - -- |
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Autoria: |
BATISTA, W. R.; SANTOS, J. E. G.; VAZ, C. M. P.; KLAR, A. E. |
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Título: |
Efeito das calibrações de um equipamento TDR para dois nitossolos vermelho distroférrico provenientes de localidades diferentes |
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Ano de publicação: |
2007 |
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Fonte/Imprenta: |
In: CONGRESSO BRASILEIRO DE CIÊNCIA DO SOLO, 31., 2007, Gramado, RS. Conquistas e desafios da ciência do solo brasileira. Livro de resumos... Porto Alegre: SBCS, 2007. p. |
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Páginas: |
294 |
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Idioma: |
Português |
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Categoria do assunto: |
-- |
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Marc: |
LEADER 00621naa a2200157 a 4500
001 1029849
005 2008-01-08
008 2007 bl --- 0-- u #d
100 1 $aBATISTA, W. R.
245 $aEfeito das calibrações de um equipamento TDR para dois nitossolos vermelho distroférrico provenientes de localidades diferentes
260 $c2007
300 $a294
700 1 $aSANTOS, J. E. G.
700 1 $aVAZ, C. M. P.
700 1 $aKLAR, A. E.
773 $tIn: CONGRESSO BRASILEIRO DE CIÊNCIA DO SOLO, 31., 2007, Gramado, RS. Conquistas e desafios da ciência do solo brasileira. Livro de resumos... Porto Alegre: SBCS, 2007. p.
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