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8HBM

Structural basis of the farnesoid X receptor/retinoid X receptor heterodimer on inverted repeat DNA

Summary for 8HBM
Entry DOI10.2210/pdb8hbm/pdb
DescriptorRetinoic acid receptor RXR-alpha, Bile acid receptor, DNA (5'-D(P*CP*CP*GP*AP*GP*GP*TP*CP*AP*AP*TP*GP*AP*CP*CP*TP*CP*G)-3'), ... (5 entities in total)
Functional Keywordsfxr, rxr, dna, dna binding protein, dna binding protein-dna complex, dna binding protein/dna
Biological sourceHomo sapiens (human)
More
Total number of polymer chains8
Total formula weight68872.15
Authors
Jiang, L.,Chen, Y. (deposition date: 2022-10-29, release date: 2023-06-14, Last modification date: 2024-05-01)
Primary citationJiang, L.,Liu, X.,Liang, X.,Dai, S.,Wei, H.,Guo, M.,Chen, Z.,Xiao, D.,Chen, Y.
Structural basis of the farnesoid X receptor/retinoid X receptor heterodimer on inverted repeat DNA.
Comput Struct Biotechnol J, 21:3149-3157, 2023
Cited by
PubMed Abstract: Farnesoid X receptor (FXR) is a ligand-activated transcription factor known as bile acid receptor (BAR). FXR plays critical roles in various biological processes, including metabolism, immune inflammation, liver regeneration and liver carcinogenesis. FXR forms a heterodimer with the retinoid X receptor (RXR) and binds to diverse FXR response elements (FXREs) to exert its various biological functions. However, the mechanism by which the FXR/RXR heterodimer binds the DNA elements remains unclear. In this study, we aimed to use structural, biochemical and bioinformatics analyses to study the mechanism of FXR binding to the typical FXRE, such as the IR1 site, and the heterodimer interactions in the FXR-DBD/RXR-DBD complex. Further biochemical assays showed that RAR, THR and NR4A2 do not form heterodimers with RXR when bound to the IR1 sites, which indicates that IR1 may be a unique binding site for the FXR/RXR heterodimer. Our studies may provide a further understanding of the dimerization specificity of nuclear receptors.
PubMed: 37287811
DOI: 10.1016/j.csbj.2023.05.026
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.3 Å)
Structure validation

237735

数据于2025-06-18公开中

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