ArticleNucleic acids research2005
eBLOCKs: enumerating conserved protein blocks to achieve maximal sensitivity and specificity.
Article in Nucleic acids research, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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Who cites it
12 citing papers in PubMed.
- Complex evolutionary footprints revealed in an analysis of reused protein segments of diverse lengths.Proceedings of the National Academy of Sciences of the United States of America · 2017Article
- A discriminative method for family-based protein remote homology detection that combines inductive logic programming and propositional models.BMC bioinformatics · 2011Article
- Article
- Protein structural modularity and robustness are associated with evolvability.Genome biology and evolution · 2011Article
- Minimotif miner 2nd release: a database and web system for motif search.Nucleic acids research · 2009Article
- A discriminative method for protein remote homology detection and fold recognition combining Top-n-grams and latent semantic analysis.BMC bioinformatics · 2008Article
- MAGIIC-PRO: detecting functional signatures by efficient discovery of long patterns in protein sequences.Nucleic acids research · 2008Article
- Motif kernel generated by genetic programming improves remote homology and fold detection.BMC bioinformatics · 2007Article
- InSite: a computational method for identifying protein-protein interaction binding sites on a proteome-wide scale.Genome biology · 2007Article
- MAGIIC-PRO: detecting functional signatures by efficient discovery of long patterns in protein sequences.Nucleic acids research · 2006Article
- Choosing negative examples for the prediction of protein-protein interactions.BMC bioinformatics · 2006Article
- QuasiMotiFinder: protein annotation by searching for evolutionarily conserved motif-like patterns.Nucleic acids research · 2005Article
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Authors and funding
4 authors.
Funding
Abstract
Classifying proteins into families and superfamilies allows identification of functionally important conserved domains. The motifs and scoring matrices derived from such conserved regions provide computational tools that recognize similar patterns in novel sequences, and thus enable the prediction of protein function for genomes. The eBLOCKs database enumerates a cascade of protein blocks with varied conservation levels for each functional domain. A biologically important region is most stringently conserved among a smaller family of highly similar proteins. The same region is often found in a larger group of more remotely related proteins with a reduced stringency. Through enumeration, highly specific signatures can be generated from blocks with more columns and fewer family members, while highly sensitive signatures can be derived from blocks with fewer columns and more members as in a superfamily. By applying PSI-BLAST and a modified K-means clustering algorithm, eBLOCKs automatically groups protein sequences according to different levels of similarity. Multiple sequence alignments are made and trimmed into a series of ungapped blocks. Motifs and position-specific scoring matrices were derived from eBLOCKs and made available for sequence search and annotation. The eBLOCKs database provides a tool for high-throughput genome annotation with maximal specificity and sensitivity. The eBLOCKs database is freely available on the World Wide Web at http://motif.stanford.edu/eblocks/ to all users for online usage. Academic and not-for-profit institutions wishing copies of the program may contact Douglas L. Brutlag (brutlag@stanford.edu). Commercial firms wishing copies of the program for internal installation may contact Jacqueline Tay at the Stanford Office of Technology Licensing (jacqueline.tay@stanford.edu; http://otl.stanford.edu/).
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