disentangling direct from indirect co-evolution of residues in protein alignments理直接从间接联合进化的残留蛋白质比对.pdfVIP

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disentangling direct from indirect co-evolution of residues in protein alignments理直接从间接联合进化的残留蛋白质比对.pdf

disentangling direct from indirect co-evolution of residues in protein alignments理直接从间接联合进化的残留蛋白质比对

Disentangling Direct from Indirect Co-Evolution of Residues in Protein Alignments Lukas Burger, Erik van Nimwegen* Biozentrum, University of Basel, and Swiss Institute of Bioinformatics, Basel, Switzerland Abstract Predicting protein structure from primary sequence is one of the ultimate challenges in computational biology. Given the large amount of available sequence data, the analysis of co-evolution, i.e., statistical dependency, between columns in multiple alignments of protein domain sequences remains one of the most promising avenues for predicting residues that are contacting in the structure. A key impediment to this approach is that strong statistical dependencies are also observed for many residue pairs that are distal in the structure. Using a comprehensive analysis of protein domains with available three-dimensional structures we show that co-evolving contacts very commonly form chains that percolate through the protein structure, inducing indirect statistical dependencies between many distal pairs of residues. We characterize the distributions of length and spatial distance traveled by these co-evolving contact chains and show that they explain a large fraction of observed statistical dependencies between structurally distal pairs. We adapt a recently developed Bayesian network model into a rigorous procedure for disentangling direct from indirect statistical dependencies, and we demonstrate that this method not only successfully accomplishes this task, but also allows contacts with weak statistical dependency to be detected. To illustrate how additional information can be incorporated into our method, we incorporate a phylogenetic correction, and we develop an informative prior that tak

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