Normalization to account for variation in urinary dilution is crucial for interpretation of urine metabolic profiles. Probabilistic quotient normalization (PQN) is used routinely in metabolomics but is sensitive to systematic variation shared across a large proportion of the spectral profile (>50%). Where ¹H nuclear magnetic resonance (NMR) spectroscopy is employed, the presence of urinary protein can elevate the spectral baseline and substantially impact the resulting profile. Using ¹H NMR...
Probing Denatured State Conformational Bias in a Three-Helix Bundle, UBA(2), Using a Cytochrome c Fusion Protein
Probing Denatured State Conformational Bias in a Three-Helix Bundle, UBA(2), Using a Cytochrome c Fusion Protein
https://pubs.acs.org/appl/literatum/publisher/achs/journals/content/bichaw/0/bichaw.ahead-of-print/acs.biochem.8b00015/20180307/images/medium/bi-2018-00015q_0007.gif
Biochemistry
DOI: 10.1021/acs.biochem.8b00015
http://feeds.feedburner.com/~ff/acs/bichaw?d=yIl2AUoC8zA
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nmrlearner
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03-08-2018 01:24 PM
[NMR paper] Probabilistic validation of protein NMR chemical shift assignments.
Probabilistic validation of protein NMR chemical shift assignments.
Probabilistic validation of protein NMR chemical shift assignments.
J Biomol NMR. 2016 Jan 2;
Authors: Dashti H, Tonelli M, Lee W, Westler WM, Cornilescu G, Ulrich EL, Markley JL
Abstract
Data validation plays an important role in ensuring the reliability and reproducibility of studies. NMR investigations of the functional properties, dynamics, chemical kinetics, and structures of proteins depend critically on the correctness of chemical shift assignments....
nmrlearner
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01-05-2016 08:23 PM
Probabilistic validation of protein NMR chemical shift assignments
Probabilistic validation of protein NMR chemical shift assignments
Abstract
Data validation plays an important role in ensuring the reliability and reproducibility of studies. NMR investigations of the functional properties, dynamics, chemical kinetics, and structures of proteins depend critically on the correctness of chemical shift assignments. We present a novel probabilistic method named ARECA for validating chemical shift assignments that relies on the nuclear Overhauser effect data . ARECA has been evaluated through its application to 26...
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01-03-2016 01:25 AM
[Question from NMRWiki Q&A forum] 1H 1D NMR data Normalization in Topspin.
1H 1D NMR data Normalization in Topspin.
I have performed a series of 1H 1D experiments with different concentration of peptide and accordingly different numbers of scans. Then in order to compare the results, I normalized the data by exporting them to text and multiplying by suitable factors. After that I tried to plot the data on excel. But the spectra are not presentable.I want to know if it is possible to normalize the data on topspin itself or any other free software??
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11-09-2015 02:00 AM
[NMR paper] Potential bias in NMR relaxation data introduced by peak intensity analysis and curve
Potential bias in NMR relaxation data introduced by peak intensity analysis and curve fitting methods.
Related Articles Potential bias in NMR relaxation data introduced by peak intensity analysis and curve fitting methods.
J Biomol NMR. 2001 Sep;21(1):1-9
Authors: Viles JH, Duggan BM, Zaborowski E, Schwarzinger S, Huntley JJ, Kroon GJ, Dyson HJ, Wright PE
We present an evaluation of the accuracy and precision of relaxation rates calculated using a variety of methods, applied to data sets obtained for several very different protein systems. We...
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11-19-2010 08:44 PM
[NMR paper] Assessing potential bias in the determination of rotational correlation times of prot
Assessing potential bias in the determination of rotational correlation times of proteins by NMR relaxation.
Related Articles Assessing potential bias in the determination of rotational correlation times of proteins by NMR relaxation.
J Biomol NMR. 1999 Feb;13(2):101-12
Authors: Lee AL, Wand AJ
The various factors that influence the reliable and efficient determination of the correlation time describing molecular reorientation of proteins by NMR relaxation methods are examined. Nuclear Overhauser effects, spin-lattice, and spin-spin relaxation...
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08-21-2010 04:03 PM
A probabilistic approach for validating protein NMR chemical shift assignments
Abstract It has been estimated that more than 20% of the proteins in the BMRB are improperly referenced and that about 1% of all chemical shift assignments are mis-assigned. These statistics also reflect the likelihood that any newly assigned protein will have shift assignment or shift referencing errors. The relatively high frequency of these errors continues to be a concern for the biomolecular NMR community. While several programs do exist to detect and/or correct chemical shift mis-referencing or chemical shift mis-assignments, most can only do one, or the other. The one program...