The High-resolution Structure of the Histidine-containing Phosphocarrier Protein HPr from Escherichia coli Determined by Restrained Molecular Dynamics from Nuclear Magnetic Resonance Nuclear Overhauser Effect Data

1994 ◽  
Vol 237 (5) ◽  
pp. 544-559 ◽  
Author(s):  
Nico A.J. van Nuland ◽  
Ilona W. Hangyi ◽  
René C. van Schaik ◽  
Herman J.C. Berendsen ◽  
Wilfred F. van Gunsteren ◽  
...  
Keyword(s):  
Escherichia Coli ◽  
Molecular Dynamics ◽  
Nuclear Magnetic Resonance ◽  
High Resolution ◽  
Nuclear Overhauser Effect ◽  
Effect Data ◽  
Overhauser Effect ◽  
High Resolution Structure ◽  
Nuclear Overhauser ◽  
Resolution Structure

Chemistry of the Podocarpaceae. XXXII. Stereochemistry of 6-Bromo-7-oxo derivatives of ring-c aromatic diterpenoids

1971 ◽  
Vol 24 (6) ◽  
pp. 1237 ◽  
Author(s):  
RC Cambie ◽  
DR Crump ◽  
WA Denny ◽  
TJ Fullerton
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Aromatic Ring ◽  
Nuclear Overhauser Effect ◽  
Optical Rotatory Dispersion ◽  
Optical Rotatory ◽  
Effect Data ◽  
Overhauser Effect ◽  
Methoxycarbonyl Group ◽  
Nuclear Overhauser ◽  
Derivatives Of

The stereochemistry of 6-bromo-7-oxo derivatives of diterpenoids possessing an aromatic ring c is discussed. Nan-stereospecific bromination of 7-oxo diterpenoids occurs for compounds with an unactivated aromatic ring provided that no methoxycarbonyl substituent is at C 4. It also occurs for a C 19 acetate providing an activating substituent is present at C 12, but not for compounds with a C 4 methoxycarbonyl group even if they possess a C 12 activating substituent. The assignment of configuration of 6-bromo substituents from nuclear magnetic resonance and nuclear Overhauser effect data is examined and limitations to the use of optical rotatory dispersion curves are discussed.

The conformational analysis of piriprost, an inhibitor of leukotriene synthesis, based on high-field nuclear magnetic resonance studies

1985 ◽  
Vol 63 (10) ◽  
pp. 2614-2617 ◽  
Author(s):  
George Kotovych ◽  
Helmut Beierbeck ◽  
David Salmon
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
High Field ◽  
Nuclear Overhauser Effect ◽  
Magnetic Resonance Studies ◽  
Effect Data ◽  
Overhauser Effect ◽  
Phenyl Rings ◽  
Nuclear Overhauser ◽  
Cyclopentene Ring

The analysis of proton nuclear Overhauser effect data for piriprost, (6,9-deepoxy)-6,9-(phenylimino)-Δ6,8 prostaglandin I1, indicates that the cyclopentene ring has the 11E conformation. A long-range nOe effect indicates that the α-chain is folded near the pyrrole and the phenyl rings.

scholarly journals Transferred nuclear Overhauser effect spectroscopy study of a peptide from the PapG pilus subunit bound by the Escherichia coli PapD chaperone

FEBS Letters ◽  
1997 ◽  
Vol 412 (1) ◽  
pp. 115-120 ◽  
Author(s):  
Björn Walse ◽  
Jan Kihlberg ◽  
Katarina Flemmer Karlsson ◽  
Mikael Nilsson ◽  
Karl-Gustav Wahlund ◽  
...  
Keyword(s):  
Escherichia Coli ◽  
Nuclear Overhauser Effect ◽  
Spectroscopy Study ◽  
Overhauser Effect ◽  
Nuclear Overhauser

A hybrid modeling strategy using Nuclear Overhauser Effect data with contact information

2012 ◽  
Vol 554 ◽  
pp. 190-194 ◽  
Author(s):  
Tae-Rae Kim ◽  
Sunyoung Ji ◽  
Sanghyuk Lee ◽  
In-Sun Chu ◽  
Seokmin Shin ◽  
...  
Keyword(s):  
Nuclear Overhauser Effect ◽  
Hybrid Modeling ◽  
Effect Data ◽  
Overhauser Effect ◽  
Contact Information ◽  
Nuclear Overhauser ◽  
Modeling Strategy
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