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ERRγ tethers strongly bisphenol A and 4-α-cumylphenol in an induced-fit manner
- Source :
- Biochemical and Biophysical Research Communications. 373:408-413
- Publication Year :
- 2008
- Publisher :
- Elsevier BV, 2008.
-
Abstract
- A receptor-binding assay and X-ray crystal structure analysis demonstrated that the endocrine disruptor bisphenol A (BPA) strongly binds to human estrogen-related receptor gamma (ERRgamma). BPA is well anchored to the ligand-binding pocket, forming hydrogen bonds with its two phenol-hydroxyl groups. In this study, we found that 4-alpha-cumylphenol lacking one of its phenol-hydroxyl groups also binds to ERRgamma very strongly. The 2.0 A crystal structure of the 4-alpha-cumylphenol/ERRgamma complex clearly revealed that ERRgamma's Leu345-beta-isopropyl plays a role in the tight binding of 4-alpha-cumylphenol and BPA, rotating in a back-and-forth induced-fit manner.
- Subjects :
- endocrine system
Bisphenol A
Protein Conformation
Biophysics
Crystal structure
Crystallography, X-Ray
Ligands
Biochemistry
chemistry.chemical_compound
Phenols
Leucine
Transcription (biology)
Chaps
Humans
Organic chemistry
Benzhydryl Compounds
Receptor
Molecular Biology
Binding Sites
urogenital system
Chemistry
Hydrogen bond
Hydrogen Bonding
Cell Biology
Receptors, Estrogen
Endocrine disruptor
Nuclear receptor
Dimerization
hormones, hormone substitutes, and hormone antagonists
Subjects
Details
- ISSN :
- 0006291X
- Volume :
- 373
- Database :
- OpenAIRE
- Journal :
- Biochemical and Biophysical Research Communications
- Accession number :
- edsair.doi.dedup.....298ec6a89be599794edef51d7e91f21c
- Full Text :
- https://doi.org/10.1016/j.bbrc.2008.06.050