The role of water molecules in stereoselectivity of glucose/galactose-binding protein
- Authors
- Kim, Minsup; Cho, Art E.
- Issue Date
- 9-11월-2016
- Publisher
- NATURE PUBLISHING GROUP
- Citation
- SCIENTIFIC REPORTS, v.6
- Indexed
- SCIE
SCOPUS
- Journal Title
- SCIENTIFIC REPORTS
- Volume
- 6
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/86852
- DOI
- 10.1038/srep36807
- ISSN
- 2045-2322
- Abstract
- Using molecular dynamics (MD) simulation methods, we attempted to explain the experimental results on ligand specificity of glucose/galactose-binding protein (GGBP) to beta-D-glucose and beta-D-galactose. For the simulation, a three-dimensional structure of GGBP was prepared, and homology modeling was performed to generate variant structures of GGBP with mutations at Asp14. Then, docking was carried out to find a reasonable beta-D-glucose and beta-D-galactose binding conformations with GGBP. Subsequent molecular dynamics simulations of beta-D-glucose-GGBP and beta-D-galactose-GGBP complexes and estimation of the orientation and stability of water molecules at the binding site revealed how water molecules influence ligand specificity. In our simulation, water molecules mediated interactions of beta-D-glucose or beta-D-galactose with residue 14 of GGBP. In this mechanism, the Phe16Ala mutant leaves both sugar molecules free to move, and the specific role of water molecules were eliminated, while the wild type, Asp14Asn mutant, and Asp14Glu mutant make hydrogen bond interactions with beta-D-glucose more favorable. Our results demonstrate that bound water molecules at the binding site of GGBP are related to localized conformational change, contributing to ligand specificity of GGBP for beta-D-glucose over beta-D-galactose.
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Collections - Graduate School > Department of Biotechnology and Bioinformatics > 1. Journal Articles
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