Compiled data set of exact NOE distance limits, residual dipolar couplings and scalar couplings for the protein GB3

  • We compiled an NMR data set consisting of exact nuclear Overhauser enhancement (eNOE) distance limits, residual dipolar couplings (RDCs) and scalar (J) couplings for GB3, which forms one of the largest and most diverse data set for structural characterization of a protein to date. All data have small experimental errors, which are carefully estimated. We use the data in the research article Vogeli et al., 2015, Complementarity and congruence between exact NOEs and traditional NMR probes for spatial decoding of protein dynamics, J. Struct. Biol., 191, 3, 306–317, doi:10.1016/j.jsb.2015.07.008 [1] for cross-validation in multiple-state structural ensemble calculation. We advocate this set to be an ideal test case for molecular dynamics simulations and structure calculations.

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Metadaten
Author:Beat VögeliORCiD, Simon OlssonORCiD, Roland RiekORCiDGND, Peter GüntertORCiDGND
URN:urn:nbn:de:hebis:30:3-771808
DOI:https://doi.org/10.1016/j.dib.2015.08.020
ISSN:2352-3409
Parent Title (English):Data in Brief
Publisher:Elsevier
Place of publication:Amsterdam
Document Type:Article
Language:English
Date of Publication (online):2015/09/16
Date of first Publication:2015/09/04
Publishing Institution:Universitätsbibliothek Johann Christian Senckenberg
Release Date:2024/03/14
Volume:5
Page Number:8
First Page:99
Last Page:106
HeBIS-PPN:521040809
Institutes:Biochemie, Chemie und Pharmazie / Biochemie und Chemie
Wissenschaftliche Zentren und koordinierte Programme / Frankfurt Institute for Advanced Studies (FIAS)
Wissenschaftliche Zentren und koordinierte Programme / Zentrum für Biomolekulare Magnetische Resonanz (BMRZ)
Dewey Decimal Classification:5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 570 Biowissenschaften; Biologie
Sammlungen:Universitätspublikationen
Licence (German):License LogoCreative Commons - CC BY - Namensnennung 4.0 International