6LIT

Estrogen-related receptor beta(ERR2) in complex with BPA

Summary for 6LIT

• Entry DOI: 10.2210/pdb6lit/pdb
• Descriptor: Steroid hormone receptor ERR2, 10-mer from Nuclear receptor coactivator 2, 4,4'-PROPANE-2,2-DIYLDIPHENOL, ... (4 entities in total)
• Functional Keywords: err2, transcription factor, bpa, transcription
• Biological source: Homo sapiens (Human); More
• Total number of polymer chains: 4
• Total formula weight: 55775.61

Authors

Yao, B.Q.,Li, Y. (deposition date: 2019-12-13, release date: 2020-10-07, Last modification date: 2023-11-22)

Primary citation

Yao, B.,Zhang, S.,Wei, Y.,Tian, S.,Lu, Z.,Jin, L.,He, Y.,Xie, W.,Li, Y.
Structural Insights into the Specificity of Ligand Binding and Coactivator Assembly by Estrogen-Related Receptor beta.
J.Mol.Biol., 432:5460-5472, 2020

PubMed Abstract: Estrogen-related receptor β (ERRβ) is a nuclear receptor critical for many biological processes. Despite the biological and pharmaceutical importance of ERRβ, deciphering the structure of ERRβ has been hampered by the difficulties in obtaining a pure and stable protein for structural studies. In fact, the ERRβ ligand-binding domain remains the last unsolved ERR structure and also one of only a few unknown nuclear receptor structures. Here, we report the identification of a critical single-residue mutation resulted in robust solubility and stability of an active ERRβ ligand-binding domain, thereby providing a protein tool enabling the first probe into the biochemical and structural studies of this important receptor. The crystal structure reveals key structural features that have enabled the integration of the molecular determinants of signals transduced across the ligand binding and coregulator recruitment by all three ERR subtypes, which also provides a framework for the rational design of selective and potent ligands for the treatment of various ERR-mediated diseases.

PubMed: 32795533
DOI: 10.1016/j.jmb.2020.08.007

Experimental method

X-RAY DIFFRACTION (2 Å)