BeStSel (Beta Structure Selection) is a novel method for the secondary structure determination and fold recognition from protein circular dichroism spectra.
 
Single spectrum analysis
and fold recognition
Secondary structure determination distinguishing parallel beta-sheets and antiparallel beta-sheets of different twists, and fold recognition from the CD spectrum.
Fold recognition
 
Prediction of fold class, architecture, topology and homology for the provided secondary structure contents.
 
Multiple spectra analysis
Analysis of a series of spectra as a function of temperature, time, ligand concentration, etc.
Secondary structure and beta-sheet decomposition for PDB structures
 
Secondary structure composition of protein structures deposited in PDB on the basis of the eight structural element decomposed by BeStSel. For comparison, DSSP data and Selcon3 decomposition is also calculated.
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References: Micsonai et al. Nucleic Acids Res. 46:W315-22 (2018),
   Micsonai et al. PNAS 112:E3095-103 (2015)
NEW: Protein Extinction Coefficient Calculator (for 205 and 214 nm).
Title: (optional)
BeStSel TUTORIAL
(PDF, 2.1 MB)
File input (text format):
OR
paste data here:
Input format:
Please enter two data columns, wavelength and CD data. Separator can be space, tab, comma or semicolon.
Please use dot as decimal point.
Example:
175   -0.47423
176   -0.35859
177   -0.25112
...
Sample spectrum
(in delta epsilon)
Input units:
delta epsilon
mean residue ellipticity
mean residue ellipticity / 1000
measured ellipticity (mdeg)
Concentration (microM):
Number of residues:
Pathlength (cm):
Please, type the characters above or use your password.