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7VNA

drosophlia AHR PAS-B domain

Summary for 7VNA
Entry DOI10.2210/pdb7vna/pdb
DescriptorAhr homolog spineless (2 entities in total)
Functional Keywordstranscription factor, ligand binding domain, transcription
Biological sourceDrosophila melanogaster (Fruit fly)
Total number of polymer chains1
Total formula weight13811.68
Authors
Dai, S.Y. (deposition date: 2021-10-10, release date: 2022-04-13, Last modification date: 2023-11-29)
Primary citationDai, S.,Qu, L.,Li, J.,Zhang, Y.,Jiang, L.,Wei, H.,Guo, M.,Chen, X.,Chen, Y.
Structural insight into the ligand binding mechanism of aryl hydrocarbon receptor.
Nat Commun, 13:6234-6234, 2022
Cited by
PubMed Abstract: The aryl hydrocarbon receptor (AHR), a member of the basic helix-loop-helix (bHLH) Per-Arnt-Sim (PAS) family of transcription factors, plays important roles in regulating xenobiotic metabolism, cellular differentiation, stem cell maintenance, as well as immunity. More recently, AHR has gained significant interest as a drug target for the development of novel cancer immunotherapy drugs. Detailed understanding of AHR-ligand binding has been hampered for decades by the lack of a three-dimensional structure of the AHR PAS-B domain. Here, we present multiple crystal structures of the Drosophila AHR PAS-B domain, including its apo, ligand-bound, and AHR nuclear translocator (ARNT) PAS-B-bound forms. Together with biochemical and cellular assays, our data reveal structural features of the AHR PAS-B domain, provide insights into the mechanism of AHR ligand binding, and provide the structural basis for the future development of AHR-targeted therapeutics.
PubMed: 36266304
DOI: 10.1038/s41467-022-33858-w
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.597 Å)
Structure validation

237735

数据于2025-06-18公开中

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