Twilight reloaded: the peptide experience

Acta Crystallogr D Struct Biol. 2017 Mar 1;73(Pt 3):211-222. doi: 10.1107/S205979831601620X. Epub 2017 Feb 28.

Abstract

The de facto commoditization of biomolecular crystallography as a result of almost disruptive instrumentation automation and continuing improvement of software allows any sensibly trained structural biologist to conduct crystallographic studies of biomolecules with reasonably valid outcomes: that is, models based on properly interpreted electron density. Robust validation has led to major mistakes in the protein part of structure models becoming rare, but some depositions of protein-peptide complex structure models, which generally carry significant interest to the scientific community, still contain erroneous models of the bound peptide ligand. Here, the protein small-molecule ligand validation tool Twilight is updated to include peptide ligands. (i) The primary technical reasons and potential human factors leading to problems in ligand structure models are presented; (ii) a new method used to score peptide-ligand models is presented; (iii) a few instructive and specific examples, including an electron-density-based analysis of peptide-ligand structures that do not contain any ligands, are discussed in detail; (iv) means to avoid such mistakes and the implications for database integrity are discussed and (v) some suggestions as to how journal editors could help to expunge errors from the Protein Data Bank are provided.

Keywords: OMIT difference density; evidence-based reasoning; protein–peptide ligand structures; validation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Algorithms
  • Animals
  • Crystallography, X-Ray
  • Data Mining
  • Databases, Protein
  • Electrons
  • Humans
  • Ligands
  • Mitogen-Activated Protein Kinase 1 / chemistry
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Molecular Conformation
  • Peptides / chemistry*
  • Peptides / metabolism
  • Phospholipases A2 / chemistry
  • Phospholipases A2 / metabolism
  • Protein Binding
  • Protein Conformation
  • Proteins / chemistry*
  • Proteins / metabolism
  • Rats
  • Serine Proteases / chemistry
  • Serine Proteases / metabolism
  • Small Molecule Libraries / chemistry*
  • Small Molecule Libraries / metabolism

Substances

  • Ligands
  • Peptides
  • Proteins
  • Small Molecule Libraries
  • Mitogen-Activated Protein Kinase 1
  • Phospholipases A2
  • Serine Proteases