Literature DB >> 8681954

NMR investigation of the solution conformation of oxidized flavodoxin from Desulfovibrio vulgaris. Determination of the tertiary structure and detection of protein-bound water molecules.

M A Knauf1, F Löhr, M Blümel, S G Mayhew, H Rüterjans.   

Abstract

Desulfovibrio vulgaris flavodoxin has been investigated with a combination of homo- and hetero-nuclear two-dimensional and three-dimensional NMR spectroscopy. The analysis of NOE, hydrogen exchange and J-coupling data led to a set of 1349 NOE, 63 hydrogen bond and 109 backbone phi-angle restraints which were used to determine the solution structure of the oxidized flavodoxin applying the distance geometry program DIANA combined with restrained energy minimization methods. Flavodoxin in solution consists of a five-stranded parallel beta-sheet which is pairwise flanked by four alpha-helices. The solution structure has been compared with the known crystal structure. While the global fold is identical, differences have been detected concerning local conformations. In addition, protein-bound water molecules have been localized by NOE effects which were detected in NMR experiments avoiding solvent suppression. The locations of these water molecules have been compared with those found in the X-ray structure.

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Year:  1996        PMID: 8681954     DOI: 10.1111/j.1432-1033.1996.0423z.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  9 in total

1.  Self-consistent 3J coupling analysis for the joint calibration of Karplus coefficients and evaluation of torsion angles.

Authors:  J M Schmidt; M Blümel; F Löhr; H Rüterjans
Journal:  J Biomol NMR       Date:  1999-05       Impact factor: 2.835

2.  Asymmetric Karplus curves for the protein side-chain 3J couplings.

Authors:  Jürgen M Schmidt
Journal:  J Biomol NMR       Date:  2007-02-27       Impact factor: 2.835

3.  Alternative E.COSY techniques for the measurement of 3J(C (i) (') (-1),C (i) (beta) ) and (3) J(H (i) (N) ,C (i) (beta) ) coupling constants in proteins.

Authors:  F Löhr; H Rüterjans
Journal:  J Biomol NMR       Date:  1999-03       Impact factor: 2.835

4.  Backbone dynamics of oxidized and reduced D. vulgaris flavodoxin in solution.

Authors:  A Hrovat; M Blümel; F Löhr; S G Mayhew; H Rüterjans
Journal:  J Biomol NMR       Date:  1997-07       Impact factor: 2.835

5.  1H, 15N and 13C NMR resonance assignment, secondary structure and global fold of the FMN-binding domain of human cytochrome P450 reductase.

Authors:  I Barsukov; S Modi; L Y Lian; K H Sze; M J Paine; C R Wolf; G C Roberts
Journal:  J Biomol NMR       Date:  1997-07       Impact factor: 2.835

6.  The electron transfer system of syntrophically grown Desulfovibrio vulgaris.

Authors:  Christopher B Walker; Zhili He; Zamin K Yang; Joseph A Ringbauer; Qiang He; Jizhong Zhou; Gerrit Voordouw; Judy D Wall; Adam P Arkin; Terry C Hazen; Sergey Stolyar; David A Stahl
Journal:  J Bacteriol       Date:  2009-07-06       Impact factor: 3.490

7.  1H, 13C and 15N assignment of the hydroquinone form of flavodoxin from Desulfovibrio vulgaris (Hildenborough) and comparison of the chemical shift differences with respect to the oxidized state.

Authors:  Gary N Yalloway; Frank Löhr; Hans L Wienk; Stephen G Mayhew; Andrea Hrovat; Martin A Knauf; Heinz Rüterjans
Journal:  J Biomol NMR       Date:  2003-03       Impact factor: 2.835

8.  Accurate quantitation of water-amide proton exchange rates using the phase-modulated CLEAN chemical EXchange (CLEANEX-PM) approach with a Fast-HSQC (FHSQC) detection scheme.

Authors:  T L Hwang; P C van Zijl; S Mori
Journal:  J Biomol NMR       Date:  1998-02       Impact factor: 2.835

Review 9.  Flavodoxins as Novel Therapeutic Targets against Helicobacter pylori and Other Gastric Pathogens.

Authors:  Sandra Salillas; Javier Sancho
Journal:  Int J Mol Sci       Date:  2020-03-10       Impact factor: 5.923

  9 in total

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