Literature DB >> 8520220

NMRPipe: a multidimensional spectral processing system based on UNIX pipes.

F Delaglio1, S Grzesiek, G W Vuister, G Zhu, J Pfeifer, A Bax.   

Abstract

The NMRPipe system is a UNIX software environment of processing, graphics, and analysis tools designed to meet current routine and research-oriented multidimensional processing requirements, and to anticipate and accommodate future demands and developments. The system is based on UNIX pipes, which allow programs running simultaneously to exchange streams of data under user control. In an NMRPipe processing scheme, a stream of spectral data flows through a pipeline of processing programs, each of which performs one component of the overall scheme, such as Fourier transformation or linear prediction. Complete multidimensional processing schemes are constructed as simple UNIX shell scripts. The processing modules themselves maintain and exploit accurate records of data sizes, detection modes, and calibration information in all dimensions, so that schemes can be constructed without the need to explicitly define or anticipate data sizes or storage details of real and imaginary channels during processing. The asynchronous pipeline scheme provides other substantial advantages, including high flexibility, favorable processing speeds, choice of both all-in-memory and disk-bound processing, easy adaptation to different data formats, simpler software development and maintenance, and the ability to distribute processing tasks on multi-CPU computers and computer networks.

Mesh:

Year:  1995        PMID: 8520220     DOI: 10.1007/BF00197809

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


  8 in total

1.  A computer-based protocol for semiautomated assignments and 3D structure determination of proteins.

Authors:  R P Meadows; E T Olejniczak; S W Fesik
Journal:  J Biomol NMR       Date:  1994-01       Impact factor: 2.835

2.  A model-free algorithm for the removal of baseline artifacts.

Authors:  M S Friedrichs
Journal:  J Biomol NMR       Date:  1995-02       Impact factor: 2.835

3.  NMR View: A computer program for the visualization and analysis of NMR data.

Authors:  B A Johnson; R A Blevins
Journal:  J Biomol NMR       Date:  1994-09       Impact factor: 2.835

4.  Modern spectrum analysis in nuclear magnetic resonance: alternatives to the Fourier transform.

Authors:  J C Hoch
Journal:  Methods Enzymol       Date:  1989       Impact factor: 1.600

5.  Automated and semiautomated analysis of homo- and heteronuclear multidimensional nuclear magnetic resonance spectra of proteins: the program Pronto.

Authors:  M Kjaer; K V Andersen; F M Poulsen
Journal:  Methods Enzymol       Date:  1994       Impact factor: 1.600

6.  Improved resolution in triple-resonance spectra by nonlinear sampling in the constant-time domain.

Authors:  P Schmieder; A S Stern; G Wagner; J C Hoch
Journal:  J Biomol NMR       Date:  1994-07       Impact factor: 2.835

7.  Application of phase sensitive two-dimensional correlated spectroscopy (COSY) for measurements of 1H-1H spin-spin coupling constants in proteins.

Authors:  D Marion; K Wüthrich
Journal:  Biochem Biophys Res Commun       Date:  1983-06-29       Impact factor: 3.575

8.  Solution structure and dynamics of ras p21.GDP determined by heteronuclear three- and four-dimensional NMR spectroscopy.

Authors:  P J Kraulis; P J Domaille; S L Campbell-Burk; T Van Aken; E D Laue
Journal:  Biochemistry       Date:  1994-03-29       Impact factor: 3.162

  8 in total
  2000 in total

1.  Structure of the phylogenetically most conserved domain of SRP RNA.

Authors:  U Schmitz; S Behrens; D M Freymann; R J Keenan; P Lukavsky; P Walter; T L James
Journal:  RNA       Date:  1999-11       Impact factor: 4.942

2.  Structural changes in the C-terminus of Ca2+-bound rat S100B (beta beta) upon binding to a peptide derived from the C-terminal regulatory domain of p53.

Authors:  R R Rustandi; D M Baldisseri; A C Drohat; D J Weber
Journal:  Protein Sci       Date:  1999-09       Impact factor: 6.725

3.  Resonance assignments of the Tn916 integrase DNA-binding domain and the integrase:DNA complex.

Authors:  K M Connolly; J M Wojciak; R T Clubb
Journal:  J Biomol NMR       Date:  1999-05       Impact factor: 2.835

4.  Assignment of the backbone resonances of oxidized Fe-superoxide dismutase, a 42 kDa paramagnet-containing enzyme.

Authors:  S Vathyam; R A Byrd; A F Miller
Journal:  J Biomol NMR       Date:  1999-07       Impact factor: 2.835

5.  Conformational ensembles: the role of neuropeptide structures in receptor binding.

Authors:  A S Edison; E Espinoza; C Zachariah
Journal:  J Neurosci       Date:  1999-08-01       Impact factor: 6.167

6.  Alternative modes of binding of proteins with tandem SH2 domains.

Authors:  R O'Brien; P Rugman; D Renzoni; M Layton; R Handa; K Hilyard; M D Waterfield; P C Driscoll; J E Ladbury
Journal:  Protein Sci       Date:  2000-03       Impact factor: 6.725

7.  Refinement of the protein backbone angle psi in NMR structure calculations.

Authors:  R Sprangers; M J Bottomley; J P Linge; J Schultz; M Nilges; M Sattler
Journal:  J Biomol NMR       Date:  2000-01       Impact factor: 2.835

8.  Inhibitor binding induces active site stabilization of the HCV NS3 protein serine protease domain.

Authors:  G Barbato; D O Cicero; F Cordier; F Narjes; B Gerlach; S Sambucini; S Grzesiek; V G Matassa; R De Francesco; R Bazzo
Journal:  EMBO J       Date:  2000-03-15       Impact factor: 11.598

9.  Backbone NMR assignments of a high molecular weight protein (47 kDa), cyclic AMP receptor protein (apo-CRP)

Authors:  H S Won; T Yamazaki; T W Lee; J G Jee; M K Yoon; S H Park; T Otomo; H Aiba; Y Kyogoku; B J Lee
Journal:  J Biomol NMR       Date:  2000-01       Impact factor: 2.835

10.  Backbone resonance assignment of the N-terminal 24 kDa fragment of the gyrase B subunit from S. aureus complexed with novobiocin.

Authors:  W Klaus; A Ross; B Gsell; H Senn
Journal:  J Biomol NMR       Date:  2000-04       Impact factor: 2.835

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