Protein structures in solution by nuclear magnetic resonance and distance geometry. The polypeptide fold of the basic pancreatic trypsin inhibitor determined using two different algorithms, DISGEO and DISMAN

Gerhard Wagner, Werner Braun, Timothy F. Havel, Thomas Schaumann, Nobuhiro Go, Kurt Wüthrich

Research output: Contribution to journalArticle

623 Scopus citations

Abstract

A set of conformational restraints derived from nuclear magnetic resonance (n.m.r.) measurements on solutions of the basic pancreatic trypsin inhibitor (BPTI) was used as input for distance geometry calculations with the programs DISGEO and DISMAN. Five structures obtained with each of these algorithms were systematically compared among themselves and with the crystal structure of BPTI. It is clear that the protein architecture observed in single crystals of BPTI is largely preserved in aqueous solution, with local structural differences mainly confined to the protein surface. The results confirm that protein conformations determined in solution by combined use of n.m.r. and distance geometry are a consequence of the experimental data and do not depend significantly on the algorithm used for the structure determination. The data obtained further provide an illustration that long intramolecular distances in proteins, which are comparable with the radius of gyration, are defined with high precision by relatively imprecise nuclear Overhauser enhancement measurements of a large number of much shorter distances.

Original languageEnglish (US)
Pages (from-to)611-639
Number of pages29
JournalJournal of Molecular Biology
Volume196
Issue number3
DOIs
StatePublished - Aug 5 1987
Externally publishedYes

ASJC Scopus subject areas

  • Structural Biology
  • Molecular Biology

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