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Related Concept Videos

Protein Folding Quality Check in the RER01:29

Protein Folding Quality Check in the RER

ER is the primary site for the maturation and folding of soluble and transmembrane secretory proteins. The calnexin cycle is a specific chaperone system that folds and assesses the confirmation of N-glycosylated proteins before they can exit the ER lumen. The primary players of this quality check pipeline are the lectins, ER-resident chaperones, and a glucosyl transferase enzyme. In case the calnexin system in the lumen fails to salvage a misfolded protein, it is transported to the cytoplasm...
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Related Experiment Video

Updated: Jun 23, 2026

Application of I TASSER, trRosetta, UCSF Chimera, HADDOCK server, and HEX loria for De Novo and In Silico Design of Proteins
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Application of I TASSER, trRosetta, UCSF Chimera, HADDOCK server, and HEX loria for De Novo and In Silico Design of Proteins

Published on: July 8, 2025

QMEAN server for protein model quality estimation.

Pascal Benkert1, Michael Künzli, Torsten Schwede

  • 1Biozentrum, University of Basel, Switzerland.

Nucleic Acids Research
|May 12, 2009
PubMed
Summary
This summary is machine-generated.

Model quality estimation is crucial for protein structure prediction. The QMEAN server offers two scoring functions, QMEAN and QMEANclust, to assess model accuracy and identify problematic regions.

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Area of Science:

  • Computational biology
  • Structural bioinformatics

Background:

  • Accurate protein structure prediction is vital for understanding biological function and disease mechanisms.
  • Selecting the most accurate model from a set of predictions is a critical step in the protein structure prediction pipeline.

Purpose of the Study:

  • To provide a web server (QMEAN) offering two validated scoring functions for protein model quality estimation.
  • To enable users to assess the global and local accuracy of protein models and identify potentially erroneous regions.

Main Methods:

  • Implementation of the QMEAN composite scoring function based on geometrical analysis of single models.
  • Development of the QMEANclust clustering-based scoring function utilizing all-against-all model comparisons.
  • Integration of these functions into a user-friendly web server for model ranking and analysis.

Main Results:

  • The QMEAN and QMEANclust scoring functions were successfully tested in the CASP8 experiment.
  • The QMEAN server provides a ranking of input protein models.
  • The server highlights regions with potential inaccuracies within each model.

Conclusions:

  • The QMEAN server offers reliable tools for assessing protein model quality.
  • Accurate model quality estimation aids in selecting the most useful protein structure predictions for downstream applications.
  • The QMEAN server facilitates the identification of potentially problematic regions, guiding further refinement or interpretation.