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Structural and functional insights into nuclear receptor signaling Jin L; Li YAdv Drug Deliv Rev 2010[Oct]; 62 (13): 1218-26Nuclear receptors are important transcriptional factors that share high sequence identity and conserved domains, including a DNA-binding domain (DBD) and a ligand-binding domain (LBD). The LBD plays a crucial role in ligand-mediated nuclear receptor activity. Hundreds of different crystal structures of nuclear receptors have revealed a general mechanism for the molecular basis of ligand binding and ligand-mediated regulation of nuclear receptors. Despite the conserved fold of nuclear receptor LBDs, the ligand-binding pocket is the least conserved region among different nuclear receptor LBDs. Structural comparison and analysis show that several features of the pocket, like the size and also the shape, have contributed to the ligand binding affinity and specificity. In addition, the plastic nature of the ligand-binding pockets in many nuclear receptors provides greater flexibility to further accommodate specific ligands with a variety of conformations. Nuclear receptor coactivators usually contain multiple LXXLL motifs that are used to interact with nuclear receptors. The nuclear receptors respond differently to distinct ligands and readily exchange their ligands in different environments. The conformational flexibility of the AF-2 helix allows the nuclear receptor to sense the presence of the bound ligands, either an agonist or an antagonist, and to recruit the coactivators or corepressors that ultimately determine the transcriptional activation or repression of nuclear receptors.|*Signal Transduction[MESH]|Cell Nucleus/*metabolism[MESH]|Humans[MESH]|Ligands[MESH]|Models, Molecular[MESH]|Molecular Structure[MESH]|Nuclear Proteins/chemistry/*metabolism[MESH]|Nuclear Receptor Coactivators/*metabolism[MESH]|Protein Conformation[MESH]|Protein Structure, Tertiary[MESH]|Receptors, Cytoplasmic and Nuclear/*chemistry/*metabolism[MESH]|Structure-Activity Relationship[MESH]|Transcription Factors/chemistry/metabolism[MESH] |
