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ELM - Functional Sites in Proteins

38428 ELM - Functional Sites in Proteins http://elm.eu.org Predicts functional sites (linear motifs) in proteins, such as post-translational modification sites, ligand motifs, and targeting signals. Context-based rules and logical filters are applied to improve predictions. Biology > Bioinformatics > Online Services > Protein Analysis protein   motif   functional   sites   sequence   disorder   predictor   prediction   loops   unstructured   unfolded   genomics   proteomics   globularity   non-globular   polypeptides   biopolymers   elm   elms Jan 6, 2008  

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Other links at Biology > Bioinformatics > Online Services > Protein Analysis

Provides protein structure information such as structural alignment, residue contact, protein-protein interfaces, contact maps and general information extraction.
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User-friendly interface allowing analysis of several proteins at once, including superimposition to deduce structural alignments, and compare active sites. From GlaxoWellcome Experimental Research, Geneva, Switzerland.
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Finds Nuclease-Associated Modular DNA-binding Domains (NUMODs) in protein sequences
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Includes WebOligoMelt (Annealing temperature of oligonucleotides), Virtual Ribosome (translate nucleotide sequences into peptides), and SeqScanGraph (graph melting temperature along nucleotide chain).
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Powerful, state-of-the-art, 2-D analysis software package with user-friendly interface from the Swiss Institute of Bioinformatics.
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Accepts a single query protein sequence and returns the most probable Gene Ontology functional annotations in each of the three ontologies.
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Search engine for visualizing 3-D biomolecular models. From the Center for Molecular Modeling, NIH, Maryland.
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In collaboration with the Munich Information Center for Protein Sequences (MIPS) and the Japanese International Protein Sequence Database (JIPID) maintains the PIR-International Protein Sequence Database --- a comprehensive, annotated, and non-redundant set of protein sequence databases in which entries are classified into family groups and alignments of each group are available.
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Prediction of beta turns and their types using statistical algorithms. 5 different methods including Chou-Fasman, Thornton's PRs, Gorbturn, and a consensus of all methods.
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Service for detecting the multiple structural alignments of proteins. Uses the common geometrical cores between the input molecules. Does not require that all the input molecules participate in the alignment.
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