Abstract

The Ramachandran plot is important to structural biology as it describes a peptide backbone in the context of its dominant degrees of freedom—the backbone dihedral angles φ and ψ (Ramachandran, Ramakrishnan & Sasisekharan, 1963). Since its introduction, the Ramachandran plot has been a crucial tool to characterize protein backbone features. However, the conformation or twist of a backbone as a function of φ and ψ has not been completely described for both cis and trans backbones. Additionally, little intuitive understanding is available about a peptide’s conformation simply from knowing the φ and ψ values of a peptide (e.g., is the regular peptide defined by φ = ψ = − 100° left-handed or right-handed?). This report provides a new metric for backbone handedness (h) based on interpreting a peptide backbone as a helix with axial displacement d and angular displacement θ, both of which are derived from a peptide backbone’s internal coordinates, especially dihedral angles φ, ψ and ω. In particular, h equals sin(θ)d∕|d|, with range [−1, 1] and negative (or positive) values indicating left(or right)-handedness. The metric h is used to characterize the handedness of every region of the Ramachandran plot for both cis (ω = 0°) and trans (ω = 180°) backbones, which provides the first exhaustive survey of twist handedness in Ramachandran (φ, ψ) space. These maps fill in the ‘dead space’ within the Ramachandran plot, which are regions that are not commonly accessed by structured proteins, but which may be accessible to intrinsically disordered proteins, short peptide fragments, and protein mimics such as peptoids. Finally, building on the work of (Zacharias & Knapp, 2013), this report presents a new plot based on d and θ that serves as a universal and intuitive alternative to the Ramachandran plot. The universality arises from the fact that the co-inhabitants of such a plot include every possible peptide backbone including cis and trans backbones. The intuitiveness arises from the fact that d and θ provide, at a glance, numerous aspects of the backbone including compactness, handedness, and planarity.

Highlights

  • The backbone of a protein (Fig. 1A) can twist and turn into numerous conformations, in part due to the amino acid sequence that the protein displays

  • The results show that the Ramachandran plot whose φ and ψ values range between 0◦ and 360◦ is more intuitive and visually meaningful, for cis backbones

  • This paper proposes a new metric for backbone handedness that depends on the sign of d and the value of θ: h = d sin(θ )

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Summary

Introduction

The backbone of a protein (Fig. 1A) can twist and turn into numerous conformations (folds), in part due to the amino acid sequence that the protein displays. Understanding how a backbone twists is of great importance to the field of biochemistry, since understanding. How to cite this article Mannige (2017), An exhaustive survey of regular peptide conformations using a new metric for backbone handedness (h). R(-1) (backboneC) α(-1) C(-1) residue N ΦΨ Cα O R(+1) Cω Cα(+1)

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