Literature DB >> 22911466

An estimate of spin diffusion in a spin subset: Application to iterative distance calculation from 3D (15)N NOESY-HMQC.

T E Malliavin1, M A Delsuc, V Y Orekhov, A S Arseniev.   

Abstract

A method for quantification of distances between amide hydrogens using only the 3D NOESY-HMQC experiment recorded on a (15)N-labelled protein is presented. This method is based on an approximate expression of the NOE intensities between amide hydrogens obtained from continuum modelling of the non-amide spins; this expression is used in a distance calculation algorithm. The algorithm has been named CROWD, standing for Continuum approximation of Relaxati On path Ways between Dilute spins. This approximation as well as the CROWD algorithm are tested on a simulated case; the CROWD algorithm is then applied to experimental data, measured on a fragment of bacteriorhodopsin.

Entities:  

Year:  1995        PMID: 22911466     DOI: 10.1007/BF00208810

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


  12 in total

1.  Relaxation matrix refinement of the solution structure of squash trypsin inhibitor.

Authors:  M Nilges; J Habazettl; A T Brünger; T A Holak
Journal:  J Mol Biol       Date:  1991-06-05       Impact factor: 5.469

2.  Solution structure of the EcoRI DNA sequence: refinement of NMR-derived distance geometry structures by NOESY spectrum back-calculations.

Authors:  W Nerdal; D R Hare; B R Reid
Journal:  Biochemistry       Date:  1989-12-26       Impact factor: 3.162

3.  Efficient analysis of protein 2D NMR spectra using the software package EASY.

Authors:  C Eccles; P Güntert; M Billeter; K Wüthrich
Journal:  J Biomol NMR       Date:  1991-07       Impact factor: 2.835

4.  Direct NOE refinement of biomolecular structures using 2D NMR data.

Authors:  A M Bonvin; R Boelens; R Kaptein
Journal:  J Biomol NMR       Date:  1991-09       Impact factor: 2.835

5.  Solution structure of a calmodulin-target peptide complex by multidimensional NMR.

Authors:  M Ikura; G M Clore; A M Gronenborn; G Zhu; C B Klee; A Bax
Journal:  Science       Date:  1992-05-01       Impact factor: 47.728

6.  [Principles of quantitative analysis of two-dimensional spectra of nuclear Overhauser effect in evaluation of protein and peptide conformation].

Authors:  A G Sobol'; A S Arsen'ev
Journal:  Bioorg Khim       Date:  1988-08

7.  Nuclear magnetic resonance solution structure of the Arc repressor using relaxation matrix calculations.

Authors:  A M Bonvin; H Vis; J N Breg; M J Burgering; R Boelens; R Kaptein
Journal:  J Mol Biol       Date:  1994-02-11       Impact factor: 5.469

8.  Sequence-specific resonance assignment and secondary structure of (1-71) bacterioopsin.

Authors:  A G Sobol; A S Arseniev; G V Abdulaeva; V F Bystrov
Journal:  J Biomol NMR       Date:  1992-03       Impact factor: 2.835

9.  Two-dimensional 1H nuclear magnetic resonance study of pike pI 5.0 parvalbumin (Esox lucius). Sequential resonance assignments and folding of the polypeptide chain.

Authors:  A Padilla; A Cavé; J Parello
Journal:  J Mol Biol       Date:  1988-12-20       Impact factor: 5.469

10.  Backbone dynamics of (1-71)bacterioopsin studied by two-dimensional 1H-15N NMR spectroscopy.

Authors:  K V Pervushin; A S Arseniev
Journal:  Eur J Biochem       Date:  1994-02-01
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