FoldHandedness
FoldHandedness analyzes and characterizes the structural properties of α-helices within protein chains using PDB-derived coordinates and DSSP helix definitions to compute interhelix angles and handedness.
Key Features:
- Helix Region Definition: Defines α-helix regions from Protein Data Bank (PDB) files using the latest version of the DSSP program for helix assignment.
- Handedness Determination: Determines the handedness for any chosen set of three helices to assess spatial chirality of helical arrangements.
- Angle and Sign Calculation: Computes the angle and the sign between pairs of selected helices to quantify their relative orientations, applicable to large proteins and complexes with DNA or RNA.
Scientific Applications:
- Analysis of large proteins and protein–nucleic acid complexes: Provides insights into spatial arrangement of α-helices that can affect mechanisms of action, stability, and interaction dynamics in assemblies involving DNA or RNA.
- Structural studies for drug design, molecular biology, and bioinformatics: Facilitates exploration of how specific helical structural features contribute to biological processes and functional hypotheses.
Methodology:
Uses PDB files as input, applies the latest DSSP program to define helix regions, and computes geometric relationships—angles, signs, and handedness—between selected helices, including determination for sets of three helices.
Topics
Details
- Tool Type:
- web application
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- Java
- Added:
- 8/3/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Pereyaslavets LB, Glyakina AV, Dovidchenko NV, Sokolovskiy IV, Galzitskaya OV. What handedness and angles between helices has the studied three-helical protein domain?. Bioinformatics. 2014;31(6):963-965. doi:10.1093/bioinformatics/btu737. PMID:25388147.
PMID: 25388147