Protein side-chain dynamics and residual conformational entropy (Q33395463)

26 July 2017

title

Protein side-chain dynamics and residual conformational entropy (English)

1 reference

26 July 2017

Nikola Trbovic

1

1 reference

26 July 2017

Jae-Hyun Cho

2

1 reference

26 July 2017

Robert Abel

3

1 reference

26 July 2017

Richard A Friesner

4

1 reference

26 July 2017

Mark Rance

5

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26 July 2017

Arthur G Palmer

6

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26 July 2017

language of work or name

English

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publication date

1 January 2009

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Journal of the American Chemical Society

26 July 2017

published in

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26 July 2017

volume

131

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26 July 2017

issue

2

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26 July 2017

page(s)

615-622

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Quantitative lid dynamics of MDM2 reveals differential ligand binding modes of the p53-binding cleft.

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14 July 2018

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14 July 2018

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Heteronuclear NMR spectroscopy for lysine NH(3) groups in proteins: unique effect of water exchange on (15)N transverse relaxation

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An inserted Gly residue fine tunes dynamics between mesophilic and thermophilic ribonucleases H

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Comparison of multiple Amber force fields and development of improved protein backbone parameters

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Characterization of the fast dynamics of protein amino acid side chains using NMR relaxation in solution

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Protein dynamics from solution NMR: theory and applications

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The penultimate rotamer library

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A study of protein side-chain dynamics from new 2H auto-correlation and 13C cross-correlation NMR experiments: application to the N-terminal SH3 domain from drk.

14 July 2018

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Accuracy and precision of NMR relaxation experiments and MD simulations for characterizing protein dynamics

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Domain packing and dynamics in the DNA complex of the N-terminal zinc fingers of TFIIIA

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14 July 2018

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Contributions to conformational entropy arising from bond vector fluctuations measured from NMR-derived order parameters: application to protein folding

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Empirical scale of side-chain conformational entropy in protein folding

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Comparison of MD Simulations and NMR Experiments for Hen Lysozyme. Analysis of Local Fluctuations, Cooperative Motions, and Global Changes

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Backbone dynamics of Escherichia coli ribonuclease HI: correlations with structure and function in an active enzyme

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Molecular dynamics simulation of E. coli ribonuclease H1 in solution: correlation with NMR and X-ray data and insights into biological function.

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A 500 ps molecular dynamics simulation study of interleukin-1 beta in water. Correlation with nuclear magnetic resonance spectroscopy and crystallography.

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Structural details of ribonuclease H from Escherichia coli as refined to an atomic resolution

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Multiple-timescale dynamics of side-chain carboxyl and carbonyl groups in proteins by 13C nuclear spin relaxation.

31 October 2018

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Multiple time scale backbone dynamics of homologous thermophilic and mesophilic ribonuclease HI enzymes

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Measurement of dipolar cross-correlation in methylene groups in uniformly 13C-, 15N-labeled proteins

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Identifiers

DOI

10.1021/JA806475K

1 reference

26 July 2017

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26 July 2017

1 reference