Molecular biology: How to determine a protein's shape Yahoo News
ABOUT 120,000 types of protein molecule have yielded up their structures to science. That sounds a lot, but it isn't. The techniques, such as X-ray crystallography and nuclear-magnetic resonance (NMR), which are used to elucidate such structures do not ...
How to determine a protein's shape - The Economist
How to determine a protein's shape - The Economist
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The Economist
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How to determine a protein's shape
The Economist
ABOUT 120,000 types of protein molecule have yielded up their structures to science. That sounds a lot, but it isn't. The techniques, such as X-ray crystallography and nuclear-magnetic resonance (NMR), which are used to elucidate such structures do not ...
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02-10-2017 03:19 AM
Using FTIR Spectroscopy to Determine Protein Secondary Structure - News-Medical.net
Using FTIR Spectroscopy to Determine Protein Secondary Structure - News-Medical.net
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Using FTIR Spectroscopy to Determine Protein Secondary Structure
News-Medical.net
Another high-resolution method is nuclear magnetic resonance (NMR) spectroscopy, which can be used to characterize protein structure in liquids. However, this method is only practical when studying small proteins, measuring 15 to 25kDa. Furthermore ...
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06-21-2016 01:09 AM
Researchers determine structure of key HIV protein - Vaccine News Daily
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Vaccine News Daily
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Researchers determine structure of key HIV protein
Vaccine News Daily
The Duke team used protein engineering, sophisticated nuclear magnetic resonance spectroscopy and specialized software to examine the dynamic intermediate step HIV uses to fuse to a host cell. While the pre- and post-fusion steps are stable and well ...
Researchers determine structure of key HIV protein - Vaccine News Daily
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01-20-2014 06:34 PM
Scientists determine structure of Ltn1 protein - News-Medical.net
Scientists determine structure of Ltn1 protein - News-Medical.net
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Scientists determine structure of Ltn1 protein
News-Medical.net
Ltn1 was deemed too large for its structure to be determined by current nuclear magnetic resonance (NMR) technology, and, as the scientists know now, too flexible to allow the highly regular crystalline packing needed by X-ray crystallographers. "It's ...
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nmrlearner
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01-17-2013 02:09 PM
Scientists Determine 1000 Protein Structures Of Deadly Diseases - Medical News Today
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Scientists Determine 1000 Protein Structures Of Deadly Diseases
Medical News Today
Working together, two scientific organizations have achieved a key milestone earlier than planned: using X-ray crystallography and nuclear magnetic resonance to probe at the atomic level, they have determined the structure of 1000 proteins from more ...
Scientists Determine 1000 Protein Structures Of Deadly Diseases - Medical News Today
More...
Impact of (15)N R(2)/R(1) Relaxation Restraints on Molecular Size, Shape, and Bond Vector Orientation for NMR Protein Structure Determination with Sparse Distance Restraints.
Impact of (15)N R(2)/R(1) Relaxation Restraints on Molecular Size, Shape, and Bond Vector Orientation for NMR Protein Structure Determination with Sparse Distance Restraints.
Impact of (15)N R(2)/R(1) Relaxation Restraints on Molecular Size, Shape, and Bond Vector Orientation for NMR Protein Structure Determination with Sparse Distance Restraints.
J Am Chem Soc. 2011 Apr 4;
Authors: Ryabov Y, Schwieters CD, Clore GM
(15)N R(2)/R(1) relaxation data contain information on molecular shape and size as well as on bond vector orientations relative to...
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04-06-2011 10:54 AM
Impact of 15N R2/R1 Relaxation Restraints on Molecular Size, Shape, and Bond Vector Orientation for NMR Protein Structure Determination with Sparse Distance Restraints
Impact of 15N R2/R1 Relaxation Restraints on Molecular Size, Shape, and Bond Vector Orientation for NMR Protein Structure Determination with Sparse Distance Restraints
Yaroslav Ryabov, Charles D. Schwieters and G. Marius Clore
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/ja201020c/aop/images/medium/ja-2011-01020c_0002.gif
Journal of the American Chemical Society
DOI: 10.1021/ja201020c
http://feeds.feedburner.com/~ff/acs/jacsat?d=yIl2AUoC8zA
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