Literature DB >> 28617580

Progressive Stereo Locking (PSL): A Residual Dipolar Coupling Based Force Field Method for Determining the Relative Configuration of Natural Products and Other Small Molecules.

Gabriel Cornilescu, René F Ramos Alvarenga1, Thomas P Wyche1,2, Tim S Bugni1, Roberto R Gil3, Claudia C Cornilescu, William M Westler, John L Markley, Charles D Schwieters4.   

Abstract

Establishing the relative configuration of a bioactive natural product represents the most challenging part in determining its structure. Residual dipolar couplings (RDCs) are sensitive probes of the relative spatial orientation of internuclear vectors. We adapted a force field structure calculation methodology to allow free sampling of both R and S configurations of the stereocenters of interest. The algorithm uses a floating alignment tensor in a simulated annealing protocol to identify the conformations and configurations that best fit experimental RDC and distance restraints (from NOE and J-coupling data). A unique configuration (for rigid molecules) or a very small number of configurations (for less rigid molecules) of the structural models having the lowest chiral angle energies and reasonable magnitudes of the alignment tensor are provided as the best predictions of the unknown configuration. For highly flexible molecules, the progressive locking of their stereocenters into their statistically dominant R or S state dramatically reduces the number of possible relative configurations. The result is verified by checking that the same configuration is obtained by initiating the locking from different regions of the molecule. For all molecules tested having known configurations (with conformations ranging from mostly rigid to highly flexible), the method accurately determined the correct configuration.

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Year:  2017        PMID: 28617580      PMCID: PMC5712214          DOI: 10.1021/acschembio.7b00281

Source DB:  PubMed          Journal:  ACS Chem Biol        ISSN: 1554-8929            Impact factor:   5.100


  32 in total

1.  The Xplor-NIH NMR molecular structure determination package.

Authors:  Charles D Schwieters; John J Kuszewski; Nico Tjandra; G Marius Clore
Journal:  J Magn Reson       Date:  2003-01       Impact factor: 2.229

2.  PRODRG: a tool for high-throughput crystallography of protein-ligand complexes.

Authors:  Alexander W Schüttelkopf; Daan M F van Aalten
Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2004-07-21

3.  Assigning stereochemistry to single diastereoisomers by GIAO NMR calculation: the DP4 probability.

Authors:  Steven G Smith; Jonathan M Goodman
Journal:  J Am Chem Soc       Date:  2010-09-22       Impact factor: 15.419

4.  Long-Range Residual Dipolar Couplings: A Tool for Determining the Configuration of Small Molecules.

Authors:  Nilamoni Nath; Edward J d'Auvergne; Christian Griesinger
Journal:  Angew Chem Int Ed Engl       Date:  2015-09-11       Impact factor: 15.336

Review 5.  Weak alignment NMR: a hawk-eyed view of biomolecular structure.

Authors:  Ad Bax; Alexander Grishaev
Journal:  Curr Opin Struct Biol       Date:  2005-10       Impact factor: 6.809

6.  Structural discrimination in small molecules by accurate measurement of long-range proton-carbon NMR residual dipolar couplings.

Authors:  Pablo Trigo-Mouriño; Armando Navarro-Vázquez; Jinfa Ying; Roberto R Gil; Ad Bax
Journal:  Angew Chem Int Ed Engl       Date:  2011-07-12       Impact factor: 15.336

7.  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

8.  Determination of the relative stereochemistry of flexible organic compounds by Ab initio methods: conformational analysis and Boltzmann-averaged GIAO 13C NMR chemical shifts.

Authors:  Giampaolo Barone; Dario Duca; Arturo Silvestri; Luigi Gomez-Paloma; Raffaele Riccio; Giuseppe Bifulco
Journal:  Chemistry       Date:  2002-07-15       Impact factor: 5.236

9.  Enzymatic total synthesis of enterocin polyketides.

Authors:  Qian Cheng; Longkuan Xiang; Miho Izumikawa; Dario Meluzzi; Bradley S Moore
Journal:  Nat Chem Biol       Date:  2007-08-12       Impact factor: 15.040

10.  The Use of a Combination of RDC and Chiroptical Spectroscopy for Determination of the Absolute Configuration of Fusariumin A from the Fungus Fusarium sp.

Authors:  Liang-Yan Liu; Han Sun; Christian Griesinger; Ji-Kai Liu
Journal:  Nat Prod Bioprospect       Date:  2016-01-20
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  6 in total

1.  Chemical Genomics, Structure Elucidation, and in Vivo Studies of the Marine-Derived Anticlostridial Ecteinamycin.

Authors:  Thomas P Wyche; René F Ramos Alvarenga; Jeff S Piotrowski; Megan N Duster; Simone R Warrack; Gabriel Cornilescu; Travis J De Wolfe; Yanpeng Hou; Doug R Braun; Gregory A Ellis; Scott W Simpkins; Justin Nelson; Chad L Myers; James Steele; Hirotada Mori; Nasia Safdar; John L Markley; Scott R Rajski; Tim S Bugni
Journal:  ACS Chem Biol       Date:  2017-07-26       Impact factor: 5.100

2.  Xplor-NIH for molecular structure determination from NMR and other data sources.

Authors:  Charles D Schwieters; Guillermo A Bermejo; G Marius Clore
Journal:  Protein Sci       Date:  2017-09-18       Impact factor: 6.725

Review 3.  Approaches to Configuration Determinations of Flexible Marine Natural Products: Advances and Prospects.

Authors:  Zong-Qing Huo; Feng Zhu; Xing-Wang Zhang; Xiao Zhang; Hong-Bao Liang; Jing-Chun Yao; Zhong Liu; Gui-Min Zhang; Qing-Qiang Yao; Guo-Fei Qin
Journal:  Mar Drugs       Date:  2022-05-19       Impact factor: 6.085

Review 4.  Residual Dipolar Couplings in Structure Determination of Natural Products.

Authors:  Gao-Wei Li; Han Liu; Feng Qiu; Xiao-Juan Wang; Xin-Xiang Lei
Journal:  Nat Prod Bioprospect       Date:  2018-06-25

5.  Configuration determination by residual dipolar couplings: accessing the full conformational space by molecular dynamics with tensorial constraints.

Authors:  Pavleta Tzvetkova; Ulrich Sternberg; Thomas Gloge; Armando Navarro-Vázquez; Burkhard Luy
Journal:  Chem Sci       Date:  2019-07-29       Impact factor: 9.825

6.  NMR-Based Configurational Assignments of Natural Products: Gibbs Sampling and Bayesian Inference Using Floating Chirality Distance Geometry Calculations.

Authors:  Stefan Immel; Matthias Köck; Michael Reggelin
Journal:  Mar Drugs       Date:  2021-12-22       Impact factor: 5.118

  6 in total

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