Literature DB >> 8111232

Statistical strategy for stereospecific hydrogen NMR assignments: validation procedures for the floating prochirality method.

R A Beckman1, S Litwin, A J Wand.   

Abstract

We examine the statistical and other considerations which determine the validity and reproducibility of stereospecific hydrogen NMR assignments obtained by the floating prochirality method. In this method, the assignment of a prochiral configuration of hydrogens at selected centers is allowed to 'float' during the structure refinement, and the distribution of prochiral orientations in highly refined structures is subjected to statistical analysis. The underlying statistical basis for this approach is examined and potential limitations of current approaches are identified. As an example, approximately 1300 distance constraints obtained from NOESY spectra of oxidized horse cytochrome c have been used to examine several computational strategies. Repeated calculations were done by several different methods on both the whole molecule (104 residues plus heme) and on a 23-residue fragment containing two helices, a turn, and flanking residues. The results show that, even with NOE constraints alone, one third of the centers may be reproducibly assigned, provided appropriate precautions are taken. These precautions include adjustments for multiple statistical comparisons and characterization of statistical interactions between prochiral centers. The analysis demonstrates that inadequately constrained systems, such as fragments from a larger molecule, may produce misleading results, raising concerns about methods which rely solely on intraresidue and sequential interresidue constraints. A mathematical model describing interactions among prochiral centers is described and validated, and protocols for assignment and statistical validation are presented.

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Year:  1993        PMID: 8111232     DOI: 10.1007/bf00198371

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


  13 in total

Review 1.  An evaluation of computational strategies for use in the determination of protein structure from distance constraints obtained by nuclear magnetic resonance.

Authors:  T F Havel
Journal:  Prog Biophys Mol Biol       Date:  1991       Impact factor: 3.667

2.  Efficient computation of three-dimensional protein structures in solution from nuclear magnetic resonance data using the program DIANA and the supporting programs CALIBA, HABAS and GLOMSA.

Authors:  P Güntert; W Braun; K Wüthrich
Journal:  J Mol Biol       Date:  1991-02-05       Impact factor: 5.469

3.  Calculation of protein conformations by proton-proton distance constraints. A new efficient algorithm.

Authors:  W Braun; N Go
Journal:  J Mol Biol       Date:  1985-12-05       Impact factor: 5.469

4.  Stereospecific assignments of side-chain protons and characterization of torsion angles in Eglin c.

Authors:  S G Hyberts; W Märki; G Wagner
Journal:  Eur J Biochem       Date:  1987-05-04

5.  Pseudo-structures for the 20 common amino acids for use in studies of protein conformations by measurements of intramolecular proton-proton distance constraints with nuclear magnetic resonance.

Authors:  K Wüthrich; M Billeter; W Braun
Journal:  J Mol Biol       Date:  1983-10-05       Impact factor: 5.469

6.  Proton resonance assignments of horse ferricytochrome c.

Authors:  Y Feng; H Roder; S W Englander; A J Wand; D L Di Stefano
Journal:  Biochemistry       Date:  1989-01-10       Impact factor: 3.162

7.  Extended X-ray absorption fine structure study of Rhodospirillum rubrum and Rhodospirillum molischianum cytochromes c': relationship between heme stereochemistry and spin state.

Authors:  Z R Korszun; G Bunker; S Khalid; W R Scheidt; M A Cusanovich; T E Meyer
Journal:  Biochemistry       Date:  1989-02-21       Impact factor: 3.162

8.  Three-dimensional structure of the wild-type lac Pribnow promoter DNA in solution. Two-dimensional nuclear magnetic resonance studies and distance geometry calculations.

Authors:  W Nerdal; D R Hare; B R Reid
Journal:  J Mol Biol       Date:  1988-06-20       Impact factor: 5.469

9.  Stereospecific nuclear magnetic resonance assignments of the methyl groups of valine and leucine in the DNA-binding domain of the 434 repressor by biosynthetically directed fractional 13C labeling.

Authors:  D Neri; T Szyperski; G Otting; H Senn; K Wüthrich
Journal:  Biochemistry       Date:  1989-09-19       Impact factor: 3.162

10.  Determining stereo-specific 1H nuclear magnetic resonance assignments from distance geometry calculations.

Authors:  P L Weber; R Morrison; D Hare
Journal:  J Mol Biol       Date:  1988-11-20       Impact factor: 5.469

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  3 in total

1.  Stereospecific assignments in proteins using exact NOEs.

Authors:  Julien Orts; Beat Vögeli; Roland Riek; Peter Güntert
Journal:  J Biomol NMR       Date:  2013-10-18       Impact factor: 2.835

2.  Floating stereospecific assignment revisited: application to an 18 kDa protein and comparison with J-coupling data.

Authors:  R H Folmer; C W Hilbers; R N Konings; M Nilges
Journal:  J Biomol NMR       Date:  1997-04       Impact factor: 2.835

Review 3.  Resonance assignment strategies for the analysis of NMR spectra of proteins.

Authors:  M F Leopold; J L Urbauer; A J Wand
Journal:  Mol Biotechnol       Date:  1994-08       Impact factor: 2.695

  3 in total

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