Search Results - "Montana, V G"
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Structural Determinants of Ligand Binding Selectivity between the Peroxisome Proliferator-Activated Receptors
Published in Proceedings of the National Academy of Sciences - PNAS (20-11-2001)“…The peroxisome proliferator-activated receptors (PPARs) are transcriptional regulators of glucose, lipid, and cholesterol metabolism. We report the x-ray…”
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2
Structural basis for autorepression of retinoid X receptor by tetramer formation and the AF-2 helix
Published in Genes & development (01-09-2000)“…The 9-cis-retinoic acid receptors (RXRalpha, RXRbeta, and RXRgamma) are nuclear receptors that play key roles in multiple hormone-signaling pathways…”
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Crystal Structure of the Glucocorticoid Receptor Ligand Binding Domain Reveals a Novel Mode of Receptor Dimerization and Coactivator Recognition
Published in Cell (12-07-2002)“…Transcriptional regulation by the glucocorticoid receptor (GR) is mediated by hormone binding, receptor dimerization, and coactivator recruitment. Here, we…”
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Structural basis for antagonist-mediated recruitment of nuclear co-repressors by PPAR α
Published in Nature (London) (07-02-2002)“…Repression of gene transcription by nuclear receptors is mediated by interactions with co-repressor proteins such as SMRT and N-CoR, which in turn recruit…”
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Asymmetry in the PPARγ/RXRα Crystal Structure Reveals the Molecular Basis of Heterodimerization among Nuclear Receptors
Published in Molecular cell (01-03-2000)“…The nuclear receptor PPAR gamma /RXR alpha heterodimer regulates glucose and lipid homeostasis and is the target for the antidiabetic drugs GI262570 and the…”
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6
Molecular Recognition of Fatty Acids by Peroxisome Proliferator–Activated Receptors
Published in Molecular cell (01-03-1999)“…The peroxisome proliferator–activated receptors (PPARs) are nuclear receptors for fatty acids (FAs) that regulate glucose and lipid homeostasis. We report the…”
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Crystal Structure of the Catalytic Domain of the Human Cell Cycle Control Phosphatase, Cdc25A
Published in Cell (15-05-1998)“…Cdc25 phosphatases activate the cell division kinases throughout the cell cycle. The 2.3 Å structure of the human Cdc25A catalytic domain reveals a small α/β…”
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Novel selective small molecule agonists for peroxisome proliferator-activated receptor δ (PPARδ)—synthesis and biological activity
Published in Bioorganic & medicinal chemistry letters (05-05-2003)“…We report the synthesis and biological activity of a new series of small molecule agonists of the human Peroxisome Proliferator-Activated Receptor δ (PPARδ)…”
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Structure-Based Design of Potent Retinoid X Receptor α Agonists
Published in Journal of medicinal chemistry (08-04-2004)“…A series of tetrahydrobenzofuranyl and tetrahydrobenzothienyl propenoic acids that showed potent agonist activity against RXRα were synthesized via a…”
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10
Asymmetry in the PPARgamma/RXRalpha crystal structure reveals the molecular basis of heterodimerization among nuclear receptors
Published in Molecular cell (01-03-2000)“…The nuclear receptor PPARgamma/RXRalpha heterodimer regulates glucose and lipid homeostasis and is the target for the antidiabetic drugs GI262570 and the…”
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11
Subtype Specific Effects of Peroxisome Proliferator-Activated Receptor Ligands on Corepressor Affinity
Published in Biochemistry (Easton) (12-08-2003)“…Natural ligands for nuclear receptors are believed to activate gene transcription by causing dissociation of corepressors and promoting the association of…”
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Alteration of a Single Amino Acid in Peroxisome Proliferator-Activated Receptor-α (PPARα) Generates a PPARδ Phenotype
Published in Molecular endocrinology (Baltimore, Md.) (01-05-2000)“…Three pharmacologically important nuclear receptors, the peroxisome proliferator-activated receptors (PPARs α,γ , and δ), mediate key transcriptional responses…”
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