Global pentapeptide statistics are far away from expected distributions
Autor: | Konrad J. Dębski, Anna Muszewska, Marta Hoffman-Sommer, Marcin Grynberg, Jarosław Poznański, Jan Topiński, Krzysztof Pawłowski |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
Protein domain Polypeptide composition lcsh:Medicine Pentapeptide repeat Article Structure-Activity Relationship 03 medical and health sciences Statistics Protein Interaction Domains and Motifs Amino Acid Sequence lcsh:Science Phylogeny Sequence (medicine) chemistry.chemical_classification Multidisciplinary Chemistry lcsh:R Proteins Composition (combinatorics) Permutation group Amino acid 030104 developmental biology Mutation Outlier lcsh:Q Oligopeptides Protein Binding |
Zdroj: | Scientific Reports, Vol 8, Iss 1, Pp 1-18 (2018) Scientific Reports |
ISSN: | 2045-2322 |
DOI: | 10.1038/s41598-018-33433-8 |
Popis: | The relationships between polypeptide composition, sequence, structure and function have been puzzling biologists ever since first protein sequences were determined. Here, we study the statistics of occurrence of all possible pentapeptide sequences in known proteins. To compensate for the non-uniform distribution of individual amino acid residues in protein sequences, we investigate separately all possible permutations of every given amino acid composition. For the majority of permutation groups we find that pentapeptide occurrences deviate strongly from the expected binomial distributions, and that the observed distributions are also characterized by high numbers of outlier sequences. An analysis of identified outliers shows they often contain known motifs and rare amino acids, suggesting that they represent important functional elements. We further compare the pentapeptide composition of regions known to correspond to protein domains with that of non-domain regions. We find that a substantial number of pentapeptides is clearly strongly favored in protein domains. Finally, we show that over-represented pentapeptides are significantly related to known functional motifs and to predicted ancient structural peptides. |
Databáze: | OpenAIRE |
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