Title | Modeling of the aryl hydrocarbon receptor (AhR) ligand binding domain and its utility in virtual ligand screening to predict new AhR ligands. |
Publication Type | Journal Article |
Year of Publication | 2009 |
Authors | Bisson, WH, Koch, DC, O'Donnell, EF, Khalil, SM, Kerkvliet, NI, Tanguay, RL, Abagyan, R, Kolluri, SKumar |
Journal | J Med Chem |
Volume | 52 |
Issue | 18 |
Pagination | 5635-41 |
Date Published | 2009 Sep 24 |
ISSN | 1520-4804 |
Keywords | Amino Acid Sequence, Animals, Cell Line, Cell Nucleus, Drug Evaluation, Preclinical, Humans, Ligands, Mice, Models, Molecular, Molecular Sequence Data, Phylogeny, Protein Conformation, Protein Structure, Tertiary, Protein Transport, Receptors, Aryl Hydrocarbon, Transcriptional Activation, User-Computer Interface |
Abstract | The aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor; the AhR Per-AhR/Arnt-Sim (PAS) domain binds ligands. We developed homology models of the AhR PAS domain to characterize previously observed intra- and interspecies differences in ligand binding using molecular docking. In silico structure-based virtual ligand screening using our model resulted in the identification of pinocembrin and 5-hydroxy-7-methoxyflavone, which promoted nuclear translocation and transcriptional activation of AhR and AhR-dependent induction of endogenous target genes. |
DOI | 10.1021/jm900199u |
Alternate Journal | J. Med. Chem. |
PubMed ID | 19719119 |
PubMed Central ID | PMC3289977 |
Grant List | T32 ES007060-20 / ES / NIEHS NIH HHS / United States P30ES00210 / ES / NIEHS NIH HHS / United States T32ES07060 / ES / NIEHS NIH HHS / United States P42 ES016465-02 / ES / NIEHS NIH HHS / United States P30 ES000210-38 / ES / NIEHS NIH HHS / United States P42 ES016465 / ES / NIEHS NIH HHS / United States T32 ES007060 / ES / NIEHS NIH HHS / United States P30 ES000210 / ES / NIEHS NIH HHS / United States |