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Profile conditional random fields for modeling protein families with structural information

A statistical model of protein families, called profile conditional random fields (CRFs), is proposed. This model may be regarded as an integration of the profile hidden Markov model (HMM) and the Finkelstein-Reva (FR) theory of protein folding. While the model structure of the profile CRF is almost...

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Autor principal: Kinjo, Akira R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Biophysical Society of Japan (BSJ) 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036637/
https://www.ncbi.nlm.nih.gov/pubmed/27857577
http://dx.doi.org/10.2142/biophysics.5.37
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author Kinjo, Akira R.
author_facet Kinjo, Akira R.
author_sort Kinjo, Akira R.
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description A statistical model of protein families, called profile conditional random fields (CRFs), is proposed. This model may be regarded as an integration of the profile hidden Markov model (HMM) and the Finkelstein-Reva (FR) theory of protein folding. While the model structure of the profile CRF is almost identical to the profile HMM, it can incorporate arbitrary correlations in the sequences to be aligned to the model. In addition, like in the FR theory, the profile CRF can incorporate long-range pair-wise interactions between model states via mean-field-like approximations. We give the detailed formulation of the model, self-consistent approximations for treating long-range interactions, and algorithms for computing partition functions and marginal probabilities. We also outline the methods for the global optimization of model parameters as well as a Bayesian framework for parameter learning and selection of optimal alignments.
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spelling pubmed-50366372016-11-17 Profile conditional random fields for modeling protein families with structural information Kinjo, Akira R. Biophysics (Nagoya-shi) Note A statistical model of protein families, called profile conditional random fields (CRFs), is proposed. This model may be regarded as an integration of the profile hidden Markov model (HMM) and the Finkelstein-Reva (FR) theory of protein folding. While the model structure of the profile CRF is almost identical to the profile HMM, it can incorporate arbitrary correlations in the sequences to be aligned to the model. In addition, like in the FR theory, the profile CRF can incorporate long-range pair-wise interactions between model states via mean-field-like approximations. We give the detailed formulation of the model, self-consistent approximations for treating long-range interactions, and algorithms for computing partition functions and marginal probabilities. We also outline the methods for the global optimization of model parameters as well as a Bayesian framework for parameter learning and selection of optimal alignments. The Biophysical Society of Japan (BSJ) 2009-05-30 /pmc/articles/PMC5036637/ /pubmed/27857577 http://dx.doi.org/10.2142/biophysics.5.37 Text en 2009 © The Biophysical Society of Japan This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Note
Kinjo, Akira R.
Profile conditional random fields for modeling protein families with structural information
title Profile conditional random fields for modeling protein families with structural information
title_full Profile conditional random fields for modeling protein families with structural information
title_fullStr Profile conditional random fields for modeling protein families with structural information
title_full_unstemmed Profile conditional random fields for modeling protein families with structural information
title_short Profile conditional random fields for modeling protein families with structural information
title_sort profile conditional random fields for modeling protein families with structural information
topic Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036637/
https://www.ncbi.nlm.nih.gov/pubmed/27857577
http://dx.doi.org/10.2142/biophysics.5.37
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