Protein structure prediction has been one of the greatest challenges in the field of computational biology and chemistry. This report presents findings on the statistical analysis of secondary structure-related patterns exhibited by non-local contact-pairs, followed by the investigation of a simple predictive model using correlated mutational behavior arising from multiple sequence alignment of homologues, whilst using PSSM as a scoring function. The initial Exploratory Data Analysis phase produced results that show some unique patterns in formation of contact-pairs observed from proteins of SCOP classes A, B, C and D. By studying the characteristics of contact-pairs in known PDB structures, mathematical functions could be devised to s...
We have previously developed a method for predicting interresidue contacts using information about c...
Correlated mutations in proteins are believed to occur in order to preserve the protein functional f...
Motivation Over the last few years, the field of protein structure prediction has been transformed b...
Protein structure prediction has been one of the greatest challenges in the field of computational b...
Item does not contain fulltextProteins with similar folds often display common patterns of residue v...
A fundamental problem in molecular biology is the prediction of the three-dimensional structure of a...
Co-evolution between pairs of residues in a multiple sequence alignment (MSA) of homologous proteins...
Correlation patterns in multiple sequence alignments of homologous proteins can be exploited to infe...
<div><p>Co-evolution between pairs of residues in a multiple sequence alignment (MSA) of homologous ...
Correlation patterns in multiple sequence alignments of homologous proteins can be exploited to infe...
† These authors contributed equally to this work Correlation patterns in multiple sequence alignment...
We have previously developed a method for predicting interresidue contacts using information about c...
<div><p>Correlation patterns in multiple sequence alignments of homologous proteins can be exploited...
ABSTRACT In this work we present a novel correlated mutations analysis (CMA) method that is signific...
Motivation: Predicting residue–residue contacts between interacting proteins is an important problem...
We have previously developed a method for predicting interresidue contacts using information about c...
Correlated mutations in proteins are believed to occur in order to preserve the protein functional f...
Motivation Over the last few years, the field of protein structure prediction has been transformed b...
Protein structure prediction has been one of the greatest challenges in the field of computational b...
Item does not contain fulltextProteins with similar folds often display common patterns of residue v...
A fundamental problem in molecular biology is the prediction of the three-dimensional structure of a...
Co-evolution between pairs of residues in a multiple sequence alignment (MSA) of homologous proteins...
Correlation patterns in multiple sequence alignments of homologous proteins can be exploited to infe...
<div><p>Co-evolution between pairs of residues in a multiple sequence alignment (MSA) of homologous ...
Correlation patterns in multiple sequence alignments of homologous proteins can be exploited to infe...
† These authors contributed equally to this work Correlation patterns in multiple sequence alignment...
We have previously developed a method for predicting interresidue contacts using information about c...
<div><p>Correlation patterns in multiple sequence alignments of homologous proteins can be exploited...
ABSTRACT In this work we present a novel correlated mutations analysis (CMA) method that is signific...
Motivation: Predicting residue–residue contacts between interacting proteins is an important problem...
We have previously developed a method for predicting interresidue contacts using information about c...
Correlated mutations in proteins are believed to occur in order to preserve the protein functional f...
Motivation Over the last few years, the field of protein structure prediction has been transformed b...