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Characterizing the regularity of tetrahedral packing motifs in protein tertiary structure
Author(s) -
Ryan Day,
Kristin P. Lennox,
David B. Dahl,
Marina Vannucci,
Jerry Tsai
Publication year - 2010
Publication title -
bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/btq573
Subject(s) - protein tertiary structure , protein data bank (rcsb pdb) , structural alignment , mathematics , tetrahedron , combinatorics , computer science , chemistry , geometry , sequence alignment , peptide sequence , stereochemistry , biochemistry , gene
While protein secondary structure is well understood, representing the repetitive nature of tertiary packing in proteins remains difficult. We have developed a construct called the relative packing group (RPG) that applies the clique concept from graph theory as a natural basis for defining the packing motifs in proteins. An RPG is defined as a clique of residues, where every member contacts all others as determined by the Delaunay tessellation. Geometrically similar RPGs define a regular element of tertiary structure or tertiary motif (TerMo). This intuitive construct provides a simple approach to characterize general repetitive elements of tertiary structure.

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