Literature DB >> 12601137

Binding free energy calculations of galectin-3-ligand interactions.

Tarun K Mandal1, Chaitali Mukhopadhyay.   

Abstract

Galectins show remarkable binding specificity towards beta-galactosides. A recently developed method for calculating binding free energies between a protein and its substrates has been used to evaluate the binding specificity of galectin-3. Five disaccharides and a tetrasaccharide were used as the substrates. The calculated binding free energies agree quite well with the experimental data and the ranking of binding affinities is well reproduced. For all the six protein-ligand complexes it was observed that electrostatic interactions oppose binding whereas the non-polar contributions drive complex formation. The observed binding specificity of galectin-3 for galactosides rather than glucosides is discussed in light of our results.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12601137     DOI: 10.1093/protein/15.12.979

Source DB:  PubMed          Journal:  Protein Eng        ISSN: 0269-2139


  2 in total

1.  The HSP90 binding mode of a radicicol-like E-oxime determined by docking, binding free energy estimations, and NMR 15N chemical shifts.

Authors:  Martin Spichty; Antoine Taly; Franz Hagn; Horst Kessler; Sofia Barluenga; Nicolas Winssinger; Martin Karplus
Journal:  Biophys Chem       Date:  2009-04-15       Impact factor: 2.352

2.  Structural Basis Underlying the Binding Preference of Human Galectins-1, -3 and -7 for Galβ1-3/4GlcNAc.

Authors:  Tung-Ju Hsieh; Hsien-Ya Lin; Zhijay Tu; Bo-Shun Huang; Shang-Chuen Wu; Chun-Hung Lin
Journal:  PLoS One       Date:  2015-05-06       Impact factor: 3.240

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.