[ASAP] Structure and Catalytic Characterization of a Second Framework Al(IV) Site in Zeolite Catalysts Revealed by NMR at 35.2 T
Structure and Catalytic Characterization of a Second Framework Al(IV) Site in Zeolite Catalysts Revealed by NMR at 35.2 T
Kuizhi Chen*†, Sarah Horstmeier‡, Vy. T. Nguyen?, Bin Wang?, Steven P. Crossley?, Tram Pham?, Zhehong Gan†, Ivan Hung†, and Jeffery L. White*§
https://pubs.acs.org/na101/home/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/jacs.0c00590/20200413/images/medium/ja0c00590_0007.gif
Journal of the American Chemical Society
DOI: 10.1021/jacs.0c00590
http://feeds.feedburner.com/~r/acs/jacsat/~4/t3FuVeVyDZo
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04-20-2020 05:10 PM
[ASAP] Selective Synergism Created by Interactive Nacre Framework-Associated Proteins Possessing EGF and vWA Motifs: Implications for Mollusk Shell Formation
Selective Synergism Created by Interactive Nacre Framework-Associated Proteins Possessing EGF and vWA Motifs: Implications for Mollusk Shell Formation
https://pubs.acs.org/appl/literatum/publisher/achs/journals/content/bichaw/0/bichaw.ahead-of-print/acs.biochem.8b00119/20180412/images/medium/bi-2018-00119s_0008.gif
Biochemistry
DOI: 10.1021/acs.biochem.8b00119
http://feeds.feedburner.com/~ff/acs/bichaw?d=yIl2AUoC8zA
http://feeds.feedburner.com/~r/acs/bichaw/~4/JVtHyAjRZKs
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04-13-2018 01:15 AM
[NMR paper] NMRFAM-SDF: a protein structure determination framework.
NMRFAM-SDF: a protein structure determination framework.
Related Articles NMRFAM-SDF: a protein structure determination framework.
J Biomol NMR. 2015 Apr 22;
Authors: Dashti H, Lee W, Tonelli M, Cornilescu CC, Cornilescu G, Assadi-Porter FM, Westler WM, Eghbalnia HR, Markley JL
Abstract
The computationally demanding nature of automated NMR structure determination necessitates a delicate balancing of factors that include the time complexity of data collection, the computational complexity of chemical shift assignments, and...
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04-23-2015 06:11 PM
NMRFAM-SDF: a protein structure determination framework
NMRFAM-SDF: a protein structure determination framework
Abstract
The computationally demanding nature of automated NMR structure determination necessitates a delicate balancing of factors that include the time complexity of data collection, the computational complexity of chemical shift assignments, and selection of proper optimization steps. During the past two decades the computational and algorithmic aspects of several discrete steps of the process have been addressed. Although no single comprehensive solution has emerged, the incorporation of a...
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04-22-2015 12:40 AM
A software framework for analysing solid-state MAS NMR data
A software framework for analysing solid-state MAS NMR data
Abstract Solid-state magic-angle-spinning (MAS) NMR of proteins has undergone many rapid methodological developments in recent years, enabling detailed studies of protein structure, function and dynamics. Software development, however, has not kept pace with these advances and data analysis is mostly performed using tools developed for solution NMR which do not directly address solid-state specific issues. Here we present additions to the CcpNmr Analysis software package which enable easier identification of spinning side...
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09-30-2011 08:01 PM
A software framework for analysing solid-state MAS NMR data.
A software framework for analysing solid-state MAS NMR data.
A software framework for analysing solid-state MAS NMR data.
J Biomol NMR. 2011 Sep 28;
Authors: Stevens TJ, Fogh RH, Boucher W, Higman VA, Eisenmenger F, Bardiaux B, van Rossum BJ, Oschkinat H, Laue ED
Abstract
Solid-state magic-angle-spinning (MAS) NMR of proteins has undergone many rapid methodological developments in recent years, enabling detailed studies of protein structure, function and dynamics. Software development, however, has not kept pace with these advances and...
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09-30-2011 06:00 AM
A software framework for analysing solid-state MAS NMR data.
A software framework for analysing solid-state MAS NMR data.
A software framework for analysing solid-state MAS NMR data.
J Biomol NMR. 2011 Sep 28;
Authors: Stevens TJ, Fogh RH, Boucher W, Higman VA, Eisenmenger F, Bardiaux B, van Rossum BJ, Oschkinat H, Laue ED
Abstract
Solid-state magic-angle-spinning (MAS) NMR of proteins has undergone many rapid methodological developments in recent years, enabling detailed studies of protein structure, function and dynamics. Software development, however, has not kept pace with these advances...
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09-30-2011 05:59 AM
[NMR paper] General framework for studying the dynamics of folded and nonfolded proteins by NMR r
General framework for studying the dynamics of folded and nonfolded proteins by NMR relaxation spectroscopy and MD simulation.
Related Articles General framework for studying the dynamics of folded and nonfolded proteins by NMR relaxation spectroscopy and MD simulation.
J Am Chem Soc. 2002 Apr 24;124(16):4522-34
Authors: Prompers JJ, Brüschweiler R
A general framework is presented for the interpretation of NMR relaxation data of proteins. The method, termed isotropic reorientational eigenmode dynamics (iRED), relies on a principal component...