999 resultados para vulnerabilidades web
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Temperature sensitive (Ts) mutants of proteins provide experimentalists with a powerful and reversible way of conditionally expressing genes. The technique has been widely used in determining the role of gene and gene products in several cellular processes. Traditionally, Ts mutants are generated by random mutagenesis and then selected though laborious large-scale screening. Our web server, TSpred (http://mspc.bii.a-star.edu.sg/TSpred/), now enables users to rationally design Ts mutants for their proteins of interest. TSpred uses hydrophobicity and hydrophobic moment, deduced from primary sequence and residue depth, inferred from 3D structures to predict/identify buried hydrophobic residues. Mutating these residues leads to the creation of Ts mutants. Our method has been experimentally validated in 36 positions in six different proteins. It is an attractive proposition for Ts mutant engineering as it proposes a small number of mutations and with high precision. The accompanying web server is simple and intuitive to use and can handle proteins and protein complexes of different sizes.
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Background: The function of a protein can be deciphered with higher accuracy from its structure than from its amino acid sequence. Due to the huge gap in the available protein sequence and structural space, tools that can generate functionally homogeneous clusters using only the sequence information, hold great importance. For this, traditional alignment-based tools work well in most cases and clustering is performed on the basis of sequence similarity. But, in the case of multi-domain proteins, the alignment quality might be poor due to varied lengths of the proteins, domain shuffling or circular permutations. Multi-domain proteins are ubiquitous in nature, hence alignment-free tools, which overcome the shortcomings of alignment-based protein comparison methods, are required. Further, existing tools classify proteins using only domain-level information and hence miss out on the information encoded in the tethered regions or accessory domains. Our method, on the other hand, takes into account the full-length sequence of a protein, consolidating the complete sequence information to understand a given protein better. Results: Our web-server, CLAP (Classification of Proteins), is one such alignment-free software for automatic classification of protein sequences. It utilizes a pattern-matching algorithm that assigns local matching scores (LMS) to residues that are a part of the matched patterns between two sequences being compared. CLAP works on full-length sequences and does not require prior domain definitions. Pilot studies undertaken previously on protein kinases and immunoglobulins have shown that CLAP yields clusters, which have high functional and domain architectural similarity. Moreover, parsing at a statistically determined cut-off resulted in clusters that corroborated with the sub-family level classification of that particular domain family. Conclusions: CLAP is a useful protein-clustering tool, independent of domain assignment, domain order, sequence length and domain diversity. Our method can be used for any set of protein sequences, yielding functionally relevant clusters with high domain architectural homogeneity. The CLAP web server is freely available for academic use at http://nslab.mbu.iisc.ernet.in/clap/.
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Background: Haemophilus influenzae (H. Influenzae) is the causative agent of pneumonia, bacteraemia and meningitis. The organism is responsible for large number of deaths in both developed and developing countries. Even-though the first bacterial genome to be sequenced was that of H. Influenzae, there is no exclusive database dedicated for H. Influenzae. This prompted us to develop the Haemophilus influenzae Genome Database (HIGDB). Methods: All data of HIGDB are stored and managed in MySQL database. The HIGDB is hosted on Solaris server and developed using PERL modules. Ajax and JavaScript are used for the interface development. Results: The HIGDB contains detailed information on 42,741 proteins, 18,077 genes including 10 whole genome sequences and also 284 three dimensional structures of proteins of H. influenzae. In addition, the database provides ``Motif search'' and ``GBrowse''. The HIGDB is freely accessible through the URL:http://bioserverl.physicslisc.ernetin/HIGDB/. Discussion: The HIGDB will be a single point access for bacteriological, clinical, genomic and proteomic information of H. influenzae. The database can also be used to identify DNA motifs within H. influenzae genomes and to compare gene or protein sequences of a particular strain with other strains of H. influenzae. (C) 2014 Elsevier Ltd. All rights reserved.
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An online computing server, Online_DPI (where DPI denotes the diffraction precision index), has been created to calculate the `Cruickshank DPI' value for a given three-dimensional protein or macromolecular structure. It also estimates the atomic coordinate error for all the atoms available in the structure. It is an easy-to-use web server that enables users to visualize the computed values dynamically on the client machine. Users can provide the Protein Data Bank (PDB) identification code or upload the three-dimensional atomic coordinates from the client machine. The computed DPI value for the structure and the atomic coordinate errors for all the atoms are included in the revised PDB file. Further, users can graphically view the atomic coordinate error along with `temperature factors' (i.e. atomic displacement parameters). In addition, the computing engine is interfaced with an up-to-date local copy of the Protein Data Bank. New entries are updated every week, and thus users can access all the structures available in the Protein Data Bank. The computing engine is freely accessible online at http://cluster.physics.iisc.ernet.in/dpi/.
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Hydrogen bonds in biological macromolecules play significant structural and functional roles. They are the key contributors to most of the interactions without which no living system exists. In view of this, a web-based computing server, the Hydrogen Bonds Computing Server (HBCS), has been developed to compute hydrogen-bond interactions and their standard deviations for any given macromolecular structure. The computing server is connected to a locally maintained Protein Data Bank (PDB) archive. Thus, the user can calculate the above parameters for any deposited structure, and options have also been provided for the user to upload a structure in PDB format from the client machine. In addition, the server has been interfaced with the molecular viewers Jmol and JSmol to visualize the hydrogen-bond interactions. The proposed server is freely available and accessible via the World Wide Web at http://bioserver1.physics.iisc.ernet.in/hbcs/.
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Resumen: Esta conferencia propone una puesta en perspectiva sociohistórica del simposio “Riesgos, desigualdades y fragmentaciones sociales vinculados al trabajo”. Eso recuerda primero que los fenómenos de fragmentación social y de vulnerabilidad adulta estuvieron, desde 1895, en el origen y la gestación de las principales corrientes de la psicología. Posteriormente se cambia a la lógica “fragmentación-vulnerabilidad” a través de los conceptos de precariedad y de vulnerabilidad psicológica. Finalmente se sugiere que, distinguiendo la fragilidad humana de la vulnerabilidad adulta, la psicología puede por un lado entender mejor la actual obsesión de prevención de los riesgos y por otra parte la oscilación adulta entre fragmentación “vulnerabilizante” y conciliación fatigante
A web-based semantic information retrieval system to support decision-making in collaborative design
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Estuda etiquetagem e folksonomia sob a óptica dos processos de organização e recuperação da informação na web. Utiliza a metodologia de revisão bibliográfica, além de estudo de usuários, pesquisa exploratória e descritiva de sítios da web.
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Impreso por la Diputación Foral de Álava, D.L. VI-430/99.
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Aponta aspectos que devem ser considerados na identificação de metadados de assunto granulares para a legislação federal brasileira. O objeto de estudo foi o Sistema de Legislação Informatizada (Legin Web) disponível no Portal da Câmara dos Deputados. Os objetivos específicos foram: identificar tipos de assuntos amplamente utilizados na indexação da legislação federal brasileira e aspectos do contexto de busca de informação que interferissem na identificação dos metadados de assunto; analisar possibilidades de metadados de assunto para a legislação federal com base em padrões de metadados e modelos de organização da informação abordados na literatura; e, com isso, propor metadados de assunto para a legislação federal brasileira. A ideia é usar esses metadados para diminuir a imprecisão dos resultados das pesquisas na legislação federal, tornando o processo mais rápido e eficiente.
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Este proyecto se basa en desarrollar una aplicación web llamada Emantake y su finalidad es facilitar la búsqueda de personas para el aprendizaje de idiomas.Para realizarlo se han utilizado diferentes lenguajes, entornos y tecnologías propios de este tipo de aplicaciones las cuales se han estudiado con detenimiento para la realización del proyecto.