Abstract

BackgroundSecondary structures are elements of great importance in structural biology, biochemistry and bioinformatics. They are broadly composed of two repetitive structures namely α-helices and β-sheets, apart from turns, and the rest is associated to coil. These repetitive secondary structures have specific and conserved biophysical and geometric properties. PolyProline II (PPII) helix is yet another interesting repetitive structure which is less frequent and not usually associated with stabilizing interactions. Recent studies have shown that PPII frequency is higher than expected, and they could have an important role in protein – protein interactions.Methodology/Principal FindingsA major factor that limits the study of PPII is that its assignment cannot be carried out with the most commonly used secondary structure assignment methods (SSAMs). The purpose of this work is to propose a PPII assignment methodology that can be defined in the frame of DSSP secondary structure assignment. Considering the ambiguity in PPII assignments by different methods, a consensus assignment strategy was utilized. To define the most consensual rule of PPII assignment, three SSAMs that can assign PPII, were compared and analyzed. The assignment rule was defined to have a maximum coverage of all assignments made by these SSAMs. Not many constraints were added to the assignment and only PPII helices of at least 2 residues length are defined.Conclusions/SignificanceThe simple rules designed in this study for characterizing PPII conformation, lead to the assignment of 5% of all amino as PPII. Sequence – structure relationships associated with PPII, defined by the different SSAMs, underline few striking differences. A specific study of amino acid preferences in their N and C-cap regions was carried out as their solvent accessibility and contact patterns. Thus the assignment of PPII can be coupled with DSSP and thus opens a simple way for further analysis in this field.

Highlights

  • The three dimensional structures of proteins are of great help to understand the precise details of its biological function

  • Comparison of the different secondary structure assignment methods (SSAMs) A non-redundant databank of protein structures has been extracted from the Protein DataBank (PDB) [6]

  • The list of protein structures has been obtained from PISCES database [61,62], which is generated based on the following criteria : resolution less than 2.5 A, R factor all (%) in DSSP coil (%) av. len. in PPIIDSSP (%)

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Summary

Introduction

The three dimensional structures of proteins are of great help to understand the precise details of its biological function. The high frequency of ahelices and b-sheets observed in experimentally determined structures [6] has led to the concept of ‘secondary structures’ which describes these local backbone regularities in the protein structure. The secondary structure description is composed mainly of a-helix, b-strand and a state corresponding to other regions in the backbone, the coil. Secondary structures are elements of great importance in structural biology, biochemistry and bioinformatics They are broadly composed of two repetitive structures namely a-helices and b-sheets, apart from turns, and the rest is associated to coil. These repetitive secondary structures have specific and conserved biophysical and geometric properties. Recent studies have shown that PPII frequency is higher than expected, and they could have an important role in protein – protein interactions

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