Cargando…
Bayesian Top-Down Protein Sequence Alignment with Inferred Position-Specific Gap Penalties
We describe a Bayesian Markov chain Monte Carlo (MCMC) sampler for protein multiple sequence alignment (MSA) that, as implemented in the program GISMO and applied to large numbers of diverse sequences, is more accurate than the popular MSA programs MUSCLE, MAFFT, Clustal-Ω and Kalign. Features of GI...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4871425/ https://www.ncbi.nlm.nih.gov/pubmed/27192614 http://dx.doi.org/10.1371/journal.pcbi.1004936 |
_version_ | 1782432588426641408 |
---|---|
author | Neuwald, Andrew F. Altschul, Stephen F. |
author_facet | Neuwald, Andrew F. Altschul, Stephen F. |
author_sort | Neuwald, Andrew F. |
collection | PubMed |
description | We describe a Bayesian Markov chain Monte Carlo (MCMC) sampler for protein multiple sequence alignment (MSA) that, as implemented in the program GISMO and applied to large numbers of diverse sequences, is more accurate than the popular MSA programs MUSCLE, MAFFT, Clustal-Ω and Kalign. Features of GISMO central to its performance are: (i) It employs a “top-down” strategy with a favorable asymptotic time complexity that first identifies regions generally shared by all the input sequences, and then realigns closely related subgroups in tandem. (ii) It infers position-specific gap penalties that favor insertions or deletions (indels) within each sequence at alignment positions in which indels are invoked in other sequences. This favors the placement of insertions between conserved blocks, which can be understood as making up the proteins’ structural core. (iii) It uses a Bayesian statistical measure of alignment quality based on the minimum description length principle and on Dirichlet mixture priors. Consequently, GISMO aligns sequence regions only when statistically justified. This is unlike methods based on the ad hoc, but widely used, sum-of-the-pairs scoring system, which will align random sequences. (iv) It defines a system for exploring alignment space that provides natural avenues for further experimentation through the development of new sampling strategies for more efficiently escaping from suboptimal traps. GISMO’s superior performance is illustrated using 408 protein sets containing, on average, 235 sequences. These sets correspond to NCBI Conserved Domain Database alignments, which have been manually curated in the light of available crystal structures, and thus provide a means to assess alignment accuracy. GISMO fills a different niche than other MSA programs, namely identifying and aligning a conserved domain present within a large, diverse set of full length sequences. The GISMO program is available at http://gismo.igs.umaryland.edu/. |
format | Online Article Text |
id | pubmed-4871425 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-48714252016-05-31 Bayesian Top-Down Protein Sequence Alignment with Inferred Position-Specific Gap Penalties Neuwald, Andrew F. Altschul, Stephen F. PLoS Comput Biol Research Article We describe a Bayesian Markov chain Monte Carlo (MCMC) sampler for protein multiple sequence alignment (MSA) that, as implemented in the program GISMO and applied to large numbers of diverse sequences, is more accurate than the popular MSA programs MUSCLE, MAFFT, Clustal-Ω and Kalign. Features of GISMO central to its performance are: (i) It employs a “top-down” strategy with a favorable asymptotic time complexity that first identifies regions generally shared by all the input sequences, and then realigns closely related subgroups in tandem. (ii) It infers position-specific gap penalties that favor insertions or deletions (indels) within each sequence at alignment positions in which indels are invoked in other sequences. This favors the placement of insertions between conserved blocks, which can be understood as making up the proteins’ structural core. (iii) It uses a Bayesian statistical measure of alignment quality based on the minimum description length principle and on Dirichlet mixture priors. Consequently, GISMO aligns sequence regions only when statistically justified. This is unlike methods based on the ad hoc, but widely used, sum-of-the-pairs scoring system, which will align random sequences. (iv) It defines a system for exploring alignment space that provides natural avenues for further experimentation through the development of new sampling strategies for more efficiently escaping from suboptimal traps. GISMO’s superior performance is illustrated using 408 protein sets containing, on average, 235 sequences. These sets correspond to NCBI Conserved Domain Database alignments, which have been manually curated in the light of available crystal structures, and thus provide a means to assess alignment accuracy. GISMO fills a different niche than other MSA programs, namely identifying and aligning a conserved domain present within a large, diverse set of full length sequences. The GISMO program is available at http://gismo.igs.umaryland.edu/. Public Library of Science 2016-05-18 /pmc/articles/PMC4871425/ /pubmed/27192614 http://dx.doi.org/10.1371/journal.pcbi.1004936 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Neuwald, Andrew F. Altschul, Stephen F. Bayesian Top-Down Protein Sequence Alignment with Inferred Position-Specific Gap Penalties |
title | Bayesian Top-Down Protein Sequence Alignment with Inferred Position-Specific Gap Penalties |
title_full | Bayesian Top-Down Protein Sequence Alignment with Inferred Position-Specific Gap Penalties |
title_fullStr | Bayesian Top-Down Protein Sequence Alignment with Inferred Position-Specific Gap Penalties |
title_full_unstemmed | Bayesian Top-Down Protein Sequence Alignment with Inferred Position-Specific Gap Penalties |
title_short | Bayesian Top-Down Protein Sequence Alignment with Inferred Position-Specific Gap Penalties |
title_sort | bayesian top-down protein sequence alignment with inferred position-specific gap penalties |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4871425/ https://www.ncbi.nlm.nih.gov/pubmed/27192614 http://dx.doi.org/10.1371/journal.pcbi.1004936 |
work_keys_str_mv | AT neuwaldandrewf bayesiantopdownproteinsequencealignmentwithinferredpositionspecificgappenalties AT altschulstephenf bayesiantopdownproteinsequencealignmentwithinferredpositionspecificgappenalties |