3OSI
Crystal structure of PPARgamma ligand binding domain in complex with tetrachloro-bisphenol A (TCBPA)
Summary for 3OSI
Entry DOI | 10.2210/pdb3osi/pdb |
Related | 3OSW |
Descriptor | Peroxisome proliferator-activated receptor gamma, 4,4'-propane-2,2-diylbis(2,6-dichlorophenol), S-1,2-PROPANEDIOL, ... (4 entities in total) |
Functional Keywords | transcription, ligand binding protein |
Biological source | Homo sapiens (human) |
Total number of polymer chains | 2 |
Total formula weight | 65361.31 |
Authors | le Maire, A.,Bourguet, W. (deposition date: 2010-09-09, release date: 2011-05-25, Last modification date: 2024-02-21) |
Primary citation | Riu, A.,Grimaldi, M.,le Maire, A.,Bey, G.,Phillips, K.,Boulahtouf, A.,Perdu, E.,Zalko, D.,Bourguet, W.,Balaguer, P. Peroxisome proliferator-activated receptor Gamma is a target for halogenated analogs of bisphenol A. Environ.Health Perspect., 119:1227-1232, 2011 Cited by PubMed Abstract: The occurrence of halogenated analogs of the xenoestrogen bisphenol A (BPA) has been recently demonstrated both in environmental and human samples. These analogs include brominated [e.g., tetrabromobisphenol A (TBBPA)] and chlorinated [e.g., tetrachlorobisphenol A (TCBPA)] bisphenols, which are both flame retardants. Because of their structural homology with BPA, such chemicals are candidate endocrine disruptors. However, their possible target(s) within the nuclear hormone receptor superfamily has remained unknown. PubMed: 21561829DOI: 10.1289/ehp.1003328 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.7 Å) |
Structure validation
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