Background: Analyzing the local sequence content in proteins, earlier we found that amino acid residue frequencies differ on various distances between amino acid positions in the sequence, assuming the existence of structural units. Methods: We used informational entropy of protein sequences to find that the structural unit of proteins is a block of adjacent amino acid residues—“information unit”. The ANIS (ANalysis of Informational Structure) method uses these information units for revealing hierarchically organized Elements of the Information Structure (ELIS) in amino acid sequences. Results: The developed mathematical apparatus gives stable results on the structural unit description even with a significant variation in the parameters. Th...
Each protein is characterized by its unique sequential order of amino acids, the so-called protein s...
to appear in Journal of Statistical PhysicsProteins are essential components of living systems, capa...
This is the published version, also available here: http://dx.doi.org/10.1063/1.3498743.Structure fl...
We have developed an approach based on information theory to compute the structural information cont...
We investigated the correlation between the Shannon information entropy, ‘sequence entropy’, with re...
We have developed a general method to compute the structure entropy of protein sequences. Structure ...
We seek to understand the interplay between amino acid sequence and local structure in proteins. Are...
We introduce sequence entropy-variability plots as a method of analyzing families of protein sequenc...
Motivation: Is protein secondary structure primarily deter-mined by local interactions between resid...
AbstractWe suggest a new simple approach for comparing the primary structure of proteins and their s...
[[abstract]]We developed a technique to compute structural entropy directly from protein sequences. ...
A comprehensive data base is analyzed to determine the Shannon information content of a protein sequ...
In this paper, entropy and auto-correlation values of main chain dihedral angles of 22,356 protein m...
Atchley WR, Wollenberg KR, Fitch WM, Terhalle W, Dress A. Correlations Among Amino Acid Sites in bHL...
Proteins are essential components of living systems, capable of performing a huge variety of tasks a...
Each protein is characterized by its unique sequential order of amino acids, the so-called protein s...
to appear in Journal of Statistical PhysicsProteins are essential components of living systems, capa...
This is the published version, also available here: http://dx.doi.org/10.1063/1.3498743.Structure fl...
We have developed an approach based on information theory to compute the structural information cont...
We investigated the correlation between the Shannon information entropy, ‘sequence entropy’, with re...
We have developed a general method to compute the structure entropy of protein sequences. Structure ...
We seek to understand the interplay between amino acid sequence and local structure in proteins. Are...
We introduce sequence entropy-variability plots as a method of analyzing families of protein sequenc...
Motivation: Is protein secondary structure primarily deter-mined by local interactions between resid...
AbstractWe suggest a new simple approach for comparing the primary structure of proteins and their s...
[[abstract]]We developed a technique to compute structural entropy directly from protein sequences. ...
A comprehensive data base is analyzed to determine the Shannon information content of a protein sequ...
In this paper, entropy and auto-correlation values of main chain dihedral angles of 22,356 protein m...
Atchley WR, Wollenberg KR, Fitch WM, Terhalle W, Dress A. Correlations Among Amino Acid Sites in bHL...
Proteins are essential components of living systems, capable of performing a huge variety of tasks a...
Each protein is characterized by its unique sequential order of amino acids, the so-called protein s...
to appear in Journal of Statistical PhysicsProteins are essential components of living systems, capa...
This is the published version, also available here: http://dx.doi.org/10.1063/1.3498743.Structure fl...