Flexible structural protein alignment by a sequence of local transformations.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 19417057.
- Also identified by DOI 10.1093/bioinformatics/btp296 and PMC identifier 2940242.
- Licence recorded as CC BY-NC.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Throughout evolution, homologous proteins have common regions that stay semi-rigid relative to each other and other parts that vary in a more noticeable way. In order to compare the increasing number of structures in the PDB, flexible geometrical alignments are needed, that are reliable and easy to use. We present a protein structure alignment method whose main feature is the ability to consider different rigid transformations at different sites, allowing for deformations beyond a global rigid transformation. The performance of the method is comparable with that of the best ones from 10 aligners tested, regarding both the quality of the alignments with respect to hand curated ones, and the classification ability. An analysis of some structure pairs from the literature that need to be matched in a flexible fashion are shown. The use of a series of local transformations can be exported to other classifiers, and a future golden protein similarity measure could benefit from it. A public server for the program is available at http://dmi.uib.es/ProtDeform/. All data used, results and examples are available at http://dmi.uib.es/people/jairo/bio/ProtDeform.
Medical subject headings
- Algorithms
- Proteins
- Sequence Alignment
- Sequence Analysis, Protein