Literature DB >> 9566311

A NOESY-HSQC simulation program, SPIRIT.

L Zhu1, H J Dyson, P E Wright.   

Abstract

A program SPIRIT (Simulation Program considering Incomplete Recovery of z magnetization and INEPT Transfer efficiency) has been developed to simulate three-dimensional NOESY-HSQC spectra. This program takes into account (1) different transfer efficiency during INEPT and reverse INEPT durations due to differential relaxation rates and 1J coupling constants; (2) the different effect of the sensitivity-enhancement scheme on CH, CH2 and CH3 systems; and (3) incomplete recovery of longitudinal magnetization between scans. The simulation program incorporates anisotropic tumbling mode for symmetric tops, and allows for differential external relaxation rates for protons. Some well-defined internal motions, such as the fast rotation of methyl groups, are taken into account. The simulation program also allows for input of multiple conformations and their relative populations to calculate the average relaxation matrix to account for slow internal motions. With the SPIRIT program, the sensitivity-enhanced NOESY-HSQC experiment can be used directly in the evaluation of the accuracy of structures, which can potentially be improved by direct refinement against the primary data.

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Year:  1998        PMID: 9566311     DOI: 10.1023/a:1008252526537

Source DB:  PubMed          Journal:  J Biomol NMR        ISSN: 0925-2738            Impact factor:   2.835


  18 in total

1.  Assignment of the proton NMR spectrum of reduced and oxidized thioredoxin: sequence-specific assignments, secondary structure, and global fold.

Authors:  H J Dyson; A Holmgren; P E Wright
Journal:  Biochemistry       Date:  1989-08-22       Impact factor: 3.162

2.  An improved NOESY simulation program for partially relaxed spectra: BIRDER.

Authors:  L Zhu; B R Reid
Journal:  J Magn Reson B       Date:  1995-03

3.  Correcting NOESY cross-peak intensities for partial relaxation effects enabling accurate distance information.

Authors:  H Liu; M Tonelli; T L James
Journal:  J Magn Reson B       Date:  1996-04

Review 4.  Determination of three-dimensional structures of proteins and nucleic acids in solution by nuclear magnetic resonance spectroscopy.

Authors:  G M Clore; A M Gronenborn
Journal:  Crit Rev Biochem Mol Biol       Date:  1989       Impact factor: 8.250

5.  Assignment of the 15N NMR spectra of reduced and oxidized Escherichia coli thioredoxin.

Authors:  K Chandrasekhar; G Krause; A Holmgren; H J Dyson
Journal:  FEBS Lett       Date:  1991-06-24       Impact factor: 4.124

6.  Crystal structure of thioredoxin from Escherichia coli at 1.68 A resolution.

Authors:  S K Katti; D M LeMaster; H Eklund
Journal:  J Mol Biol       Date:  1990-03-05       Impact factor: 5.469

7.  The spin dynamics of heteronuclear multiple-spin systems formulated in the extended strong-narrowing limit.

Authors:  L Zhu
Journal:  J Magn Reson B       Date:  1996-06

8.  NMR of enzymatically synthesized uniformly 13C15N-labeled DNA oligonucleotides.

Authors:  D P Zimmer; D M Crothers
Journal:  Proc Natl Acad Sci U S A       Date:  1995-04-11       Impact factor: 11.205

9.  High-resolution solution structures of oxidized and reduced Escherichia coli thioredoxin.

Authors:  M F Jeng; A P Campbell; T Begley; A Holmgren; D A Case; P E Wright; H J Dyson
Journal:  Structure       Date:  1994-09-15       Impact factor: 5.006

10.  A novel approach for sequential assignment of 1H, 13C, and 15N spectra of proteins: heteronuclear triple-resonance three-dimensional NMR spectroscopy. Application to calmodulin.

Authors:  M Ikura; L E Kay; A Bax
Journal:  Biochemistry       Date:  1990-05-15       Impact factor: 3.162

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  4 in total

1.  Improved simulation of NOESY spectra by RELAX-JT2 including effects of J-coupling, transverse relaxation and chemical shift anisotrophy.

Authors:  Andreas Ried; Wolfram Gronwald; Jochen M Trenner; Konrad Brunner; Klaus-Peter Neidig; Hans Robert Kalbitzer
Journal:  J Biomol NMR       Date:  2004-10       Impact factor: 2.835

2.  Structure refinement and membrane positioning of selectively labeled OmpX in phospholipid nanodiscs.

Authors:  Franz Hagn; Gerhard Wagner
Journal:  J Biomol NMR       Date:  2014-11-28       Impact factor: 2.835

Review 3.  Quality assessment of protein NMR structures.

Authors:  Antonio Rosato; Roberto Tejero; Gaetano T Montelione
Journal:  Curr Opin Struct Biol       Date:  2013-09-21       Impact factor: 6.809

4.  Deuterated protein folds obtained directly from unassigned nuclear overhauser effect data.

Authors:  Guillermo A Bermejo; Miguel Llinás
Journal:  J Am Chem Soc       Date:  2008-03-05       Impact factor: 15.419

  4 in total

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