Carnegie Mellon University
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Structure Learning for Generative Models of Protein Fold Families

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posted on 2001-08-01, 00:00 authored by Sivaraman Balakrishnan, Hetunandan Kamisetty, Jaime G. Carbonell, Christopher J. Langmead
Statistical models of the amino acid composition of the proteins within a fold family are widely used in science and engineering. Existing techniques for learning probabilistic graphical models from multiple sequence alignments either make strong assumptions about the conditional independencies within the model (e.g., HMMs), or else use sub-optimal algorithms to learn the structure and parameters of the model. We introduce an approach to learning the topological structure and parameters of an undirected probabilistic graphical model. The learning algorithm uses block- L1 regularization and solves a convex optimization problem, thus guaranteeing a globally optimal solution at convergence. The resulting model encodes both the position-specific conservation statistics and the correlated mutation statistics between sequential and long-range pairs of residues. Our model is generative, allowing for the design of new proteins that have corresponding statistical properties to those seen in nature. We apply our approach to two widely studied protein families: the WW and the PDZ folds. We demonstrate that our model is able to capture interactions that are important in folding and allostery. Our results additionally indicate that while the network of interactions within a protein is sparse, it is richer than previously believed.

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Publisher Statement

© ACM, 2002. This is the author's version of the work. It is posted here by permission of ACM for your personal use. Not for redistribution. The definitive version was published in ACM Transactions on Computational Logic, Vol. 3, No. 4, October 2002, Pages 604–627} http://doi.acm.org/10.1145/566385.566390

Date

2001-08-01

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