In our previous work, we proposed a new way to represent protein native states, using ensembles of a small number of conformations with relative Populations, or ESP in short. Using Ubiquitin as an example, we showed that using a small number of conformations could greatly reduce the potential of overfitting and assigning relative populations to protein ensembles could significantly improve their quality. To demonstrate that ESP indeed is an excellent alternative to represent protein native states, in this work we compare the quality of two ESP ensembles of Ubiquitin with several well-known regular ensembles or average structure representations. Extensive amount of significant experimental data are employed to achieve a thorough assessment. Our results demonstrate that ESP ensembles, though much smaller in size comparing to regular ensembles, perform equally or even better sometimes in all four different types of experimental data used in the assessment, namely, the residual dipolar couplings, residual chemical shift anisotropy, hydrogen exchange rates, and solution scattering profiles. This work further underlines the significance of having relative populations in describing the native states.
[NMR images] unlike proton nmr spectroscopy the relative strength of carbon nmr
http://www2.chemistry.msu.edu/faculty/reusch/VirtTxtJml/Spectrpy/nmr/Images/ccamphor.gif
3/06/2014 10:43:59 AM GMT
unlike proton nmr spectroscopy the relative strength of carbon nmr
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nmrlearner
NMR pictures
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06-03-2014 10:43 AM
[Question from NMRWiki Q&A forum] Relative quantification (residual solvents)
Relative quantification (residual solvents)
Hi All,
I've been trying to get a clear answer to this question for a while now, but can't seem to get a definitive answer. My approach is following the method described in "Practical NMR for organic chemists" by John Hollerton and Steve Richards. I don't take any issue with this method, by only problem is that it gives a WILDLY different answer to the one I obtain when I do NMR quantification in TopSpin... this is a big problem, since often we are interested in the % of unwanted molecules in our samples.
Let me give you a simplified...
nmrlearner
News from other NMR forums
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10-31-2013 12:05 AM
[NMR paper] In-Cell NMR Characterization of the Secondary Structure Populations of a Disordered Conformation of ?-Synuclein within E. coli Cells.
In-Cell NMR Characterization of the Secondary Structure Populations of a Disordered Conformation of ?-Synuclein within E. coli Cells.
In-Cell NMR Characterization of the Secondary Structure Populations of a Disordered Conformation of ?-Synuclein within E. coli Cells.
PLoS One. 2013;8(8):e72286
Authors: Waudby CA, Camilloni C, Fitzpatrick AW, Cabrita LD, Dobson CM, Vendruscolo M, Christodoulou J
Abstract
?-Synuclein is a small protein strongly implicated in the pathogenesis of Parkinson's disease and related neurodegenerative disorders. We...
nmrlearner
Journal club
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08-31-2013 06:56 PM
[NMR paper] Low resolution (1)H NMR assignment of proton populations in pound cake and its polymeric ingredients.
Low resolution (1)H NMR assignment of proton populations in pound cake and its polymeric ingredients.
Related Articles Low resolution (1)H NMR assignment of proton populations in pound cake and its polymeric ingredients.
Food Chem. 2013 Aug 15;139(1-4):120-8
Authors: Luyts A, Wilderjans E, Waterschoot J, Van Haesendonck I, Brijs K, Courtin CM, Hills B, Delcour JA
Abstract
Based on a model system approach, five different proton populations were distinguished in pound cake crumb using one dimensional low resolution (1)H NMR spectroscopy. In...
nmrlearner
Journal club
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04-09-2013 06:31 PM
Diffusivitaet Relative Anisotropie.jpg
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Diffusivitaet Relative Anisotropie.jpg
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nmrlearner
NMR pictures
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01-03-2012 01:42 PM
[NMR paper] Relative stability of protein structures determined by X-ray crystallography or NMR s
Relative stability of protein structures determined by X-ray crystallography or NMR spectroscopy: a molecular dynamics simulation study.
Related Articles Relative stability of protein structures determined by X-ray crystallography or NMR spectroscopy: a molecular dynamics simulation study.
Proteins. 2003 Oct 1;53(1):111-20
Authors: Fan H, Mark AE
The relative stability of protein structures determined by either X-ray crystallography or nuclear magnetic resonance (NMR) spectroscopy has been investigated by using molecular dynamics simulation...
nmrlearner
Journal club
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11-24-2010 09:16 PM
[NMR paper] The relative orientation of Gla and EGF domains in coagulation factor X is altered by
The relative orientation of Gla and EGF domains in coagulation factor X is altered by Ca2+ binding to the first EGF domain. A combined NMR-small angle X-ray scattering study.
http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--pubs.acs.org-images-acspubs.jpg Related Articles The relative orientation of Gla and EGF domains in coagulation factor X is altered by Ca2+ binding to the first EGF domain. A combined NMR-small angle X-ray scattering study.
Biochemistry. 1996 Sep 10;35(36):11547-59
Authors: Sunnerhagen M, Olah GA, Stenflo J, Forsén S,...
nmrlearner
Journal club
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08-22-2010 02:20 PM
[U. of Ottawa NMR Facility Blog] E.COSY and the Relative Signs of Coupling Constants
E.COSY and the Relative Signs of Coupling Constants
Spin-spin coupling constants can have values greater than or less than zero. The absolute sign of the coupling constants cannot be discerned from the simple examination of a 1H NMR spectrum. The E.COSY1 (Exclusive COrrelation SpectroscopY) technique is one method which can be used to determine the relative signs of coupling constants. E.COSY is a phase sensitive COSY variant which produces off-diagonal signals showing only the active coupling (i.e. the coupling directly responsible for the cross-peak) as 2x2 antiphase square tetrads...