Related ArticlesAccuracy and robustness of three-way decomposition applied to NMR data.
J Magn Reson. 2005 Jun;174(2):188-99
Authors: Luan T, Orekhov VY, Gutmanas A, Billeter M
Three-way decomposition is a very versatile analysis tool with applications in a variety of protein NMR fields. It has been used to extract structural data from 3D NOESYs, to determine relaxation rates in large proteins, to identify ligand binding in screening for lead compounds, and to complement non-uniformly recorded (sparse) spectra. All applications so far concerned experimental data sets; it thus remains to address questions of accuracy and robustness of the method using simulated data where the correct answer is known. Systematic tests are presented for relaxation and NOESY data sets. Mixtures of real and synthetic data are used to allow control of various parameters and comparisons with correct reference data, while working with input that is as realistic as possible. The influence of the following parameters is evaluated: signal-to-noise, overlap of signals and the use of a regularization procedure within the algorithm. The main criteria used for the evaluation are accuracy and precision. It is shown that deterioration of accuracy is indicated by internal checks such as decrease of precision. Both with relaxation data and when interpreting NOESY spectra, three-way decomposition exhibits a robust behavior in situations with severe signal overlap and/or poor signal-to-noise, e.g., by avoiding false positives in the NOE shapes of NOESY decompositions. As a complement to this study, three-way decomposition is compared to other methods that achieve the same type of results.
Structural Characterisation of a Histone Domain by Projection-Decomposition
Structural Characterisation of a Histone Domain by Projection-Decomposition
Publication year: 2012
Source: Journal of Magnetic Resonance, Available online 23 February 2012</br>
Jonas*Fredriksson, Wolfgang*Bermel, Martin*Billeter</br>
We demonstrate that two projection experiments, aN-HSQC–NOESY–N-HSQC and aC-HSQC–NOESY–N-HSQC, recorded for a histone domain from yeast, contain enough information to support a structural characterisation of the protein. At the temperature used, 298K, the histone domain exhibits a very high extent of chemical shift degeneracy that is uncharacteristic for...
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02-25-2012 04:20 PM
Analysis of non-uniformly sampled spectra with Multi-Dimensional Decomposition
Analysis of non-uniformly sampled spectra with Multi-Dimensional Decomposition
Publication year: 2011
Source: Progress in Nuclear Magnetic Resonance Spectroscopy, In Press, Accepted Manuscript, Available online 24 February 2011</br>
Vladislav Yu., Orekhov , Victor A., Jaravine</br>
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02-26-2011 01:07 PM
[NMR paper] Assessing precision and accuracy of protein structures derived from NMR data.
Assessing precision and accuracy of protein structures derived from NMR data.
Related Articles Assessing precision and accuracy of protein structures derived from NMR data.
Proteins. 2005 Jun 1;59(4):655-61
Authors: Snyder DA, Bhattacharya A, Huang YJ, Montelione GT
nmrlearner
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11-25-2010 08:21 PM
[NMR paper] Optimizing resolution in multidimensional NMR by three-way decomposition.
Optimizing resolution in multidimensional NMR by three-way decomposition.
Related Articles Optimizing resolution in multidimensional NMR by three-way decomposition.
J Biomol NMR. 2003 Oct;27(2):165-73
Authors: Orekhov VY, Ibraghimov I, Billeter M
Resolution depends on the number of points sampled in a FID; in indirectly detected dimensions it is an important determinant of the total experiment time. Based on the high redundancy present in NMR data, we propose the following timesaving scheme for three-dimensional spectra. An extensive grid of...
Precision and Accuracy of NMR Structures - PSI
Precision and Accuracy of NMR Structures - a presentation by the Protein Structure Initiative - is available to read from here:
http://journals.iucr.org/services/nmr/precision.pdf
More information about the PSI can be found here:
http://www.structuralgenomics.org/
Rachel
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09-10-2008 05:32 PM
PRODECOMP - program for decomposition of NMR spectra with coupled evolution periods
Multiway Decomposition of NMR Spectra with Coupled Evolution Periods
Daniel Malmodin and Martin Billeter
J. Am. Chem. Soc.; 2005; 127(39), pp 13486 - 13487
http://pubs.acs.org/isubscribe/journals/jacsat/127/i39/figures/ja0545822n00001.gif
Abstract:
Coupling evolution periods in NMR experiments on proteins has recently attracted much attention for its substantial savings in measurement time. Using the concept of multiway decomposition, which already proved useful in many types of NMR applications, the novel tool PRODECOMP decomposes sets of spectra with coupled evolution periods...