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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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Registro Completo
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Biblioteca(s): |
Embrapa Soja. |
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Data corrente: |
12/09/2011 |
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Data da última atualização: |
03/10/2011 |
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Tipo da produção científica: |
Artigo em Anais de Congresso |
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Autoria: |
MONTEIRO, P. M. F. O; MELLO FILHO, O. L.; NEIVA, L. C. S.; NUNES, M. R.; NUNES JÚNIOR, J.; TOLEDO, R. M. C. P.; VIEIRA, N. E.; FARIAS NETO, A. L.; MOREIRA, C. T.; MEYER, M. C.; SEII, A. H.; CÂMARA, A. R.; VAZ BISNETA, M. |
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Afiliação: |
P. M. F. O MONTEIRO, Emater-GO; ODILON LEMOS DE MELLO FILHO, CNPSO; L. C. S. NEIVA, Emater-GO; M. R. NUNES, Emater-GO; J. NUNES JÚNIOR, CTPA; R. M. C. P. TOLEDO, Emater-GO; N. E. VIEIRA, CTPA; AUSTECLINIO LOPES DE FARIAS NETO, CPAMT; CLAUDETE TEIXEIRA MOREIRA, CPAC; MAURICIO CONRADO MEYER, CNPSO; A. H. SEII, CTPA; A. R. CÂMARA, CTPA; M. VAZ BISNETA, Universidade Federal de Goiás. |
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Título: |
Extensão de registro da cultivar de soja BRSGO 8360 para Bahia e Maranhão. |
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Ano de publicação: |
2011 |
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Fonte/Imprenta: |
In: REUNIÃO DE PESQUISA DE SOJA DA REGIÃO CENTRAL DO BRASIL, 32., 2011, São Pedro, SP. Resumos expandidos... Londrina: Embrapa Soja, 2011. p. 286-287. Editado por Adilson de Oliveira Junior, Odilon Ferreira Saraiva, Regina Maria Villas Bôas de Campos Leite. |
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Idioma: |
Português |
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Thesagro: |
Soja; Variedade. |
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Thesaurus NAL: |
Cultivars; Soybeans; Varieties. |
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Categoria do assunto: |
G Melhoramento Genético |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/41804/1/monteirop.286-287.pdf
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Marc: |
LEADER 01042nam a2200301 a 4500
001 1900166
005 2011-10-03
008 2011 bl uuuu u00u1 u #d
100 1 $aMONTEIRO, P. M. F. O
245 $aExtensão de registro da cultivar de soja BRSGO 8360 para Bahia e Maranhão.
260 $aIn: REUNIÃO DE PESQUISA DE SOJA DA REGIÃO CENTRAL DO BRASIL, 32., 2011, São Pedro, SP. Resumos expandidos... Londrina: Embrapa Soja, 2011. p. 286-287. Editado por Adilson de Oliveira Junior, Odilon Ferreira Saraiva, Regina Maria Villas Bôas de Campos Leite.$c2011
650 $aCultivars
650 $aSoybeans
650 $aVarieties
650 $aSoja
650 $aVariedade
700 1 $aMELLO FILHO, O. L.
700 1 $aNEIVA, L. C. S.
700 1 $aNUNES, M. R.
700 1 $aNUNES JÚNIOR, J.
700 1 $aTOLEDO, R. M. C. P.
700 1 $aVIEIRA, N. E.
700 1 $aFARIAS NETO, A. L.
700 1 $aMOREIRA, C. T.
700 1 $aMEYER, M. C.
700 1 $aSEII, A. H.
700 1 $aCÂMARA, A. R.
700 1 $aVAZ BISNETA, M.
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Embrapa Soja (CNPSO) |
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