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The J-UNIO protocol for automated protein structure determination by NMR in solution

Academic Article
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Overview

authors

  • Serrano-Navarro, Pedro
  • Pedrini, B.
  • Mohanty, B.
  • Geralt, M.
  • Herrmann, T.
  • Wuthrich, Kurt

publication date

  • 2012

journal

  • Journal of Biomolecular NMR  Journal

abstract

  • The J-UNIO (JCSG protocol using the software UNIO) procedure for automated protein structure determination by NMR in solution is introduced. In the present implementation, J-UNIO makes use of APSY-NMR spectroscopy, 3D heteronuclear-resolved [(1)H,(1)H]-NOESY experiments, and the software UNIO. Applications with proteins from the JCSG target list with sizes up to 150 residues showed that the procedure is highly robust and efficient. In all instances the correct polypeptide fold was obtained in the first round of automated data analysis and structure calculation. After interactive validation of the data obtained from the automated routine, the quality of the final structures was comparable to results from interactive structure determination. Special advantages are that the NMR data have been recorded with 6-10 days of instrument time per protein, that there is only a single step of chemical shift adjustments to relate the backbone signals in the APSY-NMR spectra with the corresponding backbone signals in the NOESY spectra, and that the NOE-based amino acid side chain chemical shift assignments are automatically focused on those residues that are heavily weighted in the structure calculation. The individual working steps of J-UNIO are illustrated with the structure determination of the protein YP_926445.1 from Shewanella amazonensis, and the results obtained with 17 JCSG targets are critically evaluated.

subject areas

  • Amino Acid Sequence
  • Bacterial Proteins
  • Models, Molecular
  • Molecular Sequence Data
  • Nuclear Magnetic Resonance, Biomolecular
  • Protein Conformation
  • Proteins
  • Shewanella
  • Software
  • Solutions
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Identity

PubMed Central ID

  • PMC3541938

International Standard Serial Number (ISSN)

  • 0925-2738

Digital Object Identifier (DOI)

  • 10.1007/s10858-012-9645-2

PubMed ID

  • 22752932
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Additional Document Info

start page

  • 341

end page

  • 354

volume

  • 53

issue

  • 4

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