Crystal Structures of the Human Peroxisome Proliferator-Activated Receptor (PPAR)α Ligand-Binding Domain in Complexes with a Series of Phenylpropanoic Acid Derivatives Generated by a Ligand-Exchange Soaking Method
Author:
Affiliation:
1. Faculty of Life and Environmental Sciences, University of Yamanashi
2. Laboratory of Health Chemistry, Showa Pharmaceutical University
3. Lead Exploration Unit, Drug Discovery Initiative, The University of Tokyo
Publisher
Pharmaceutical Society of Japan
Subject
Pharmaceutical Science,Pharmacology,General Medicine
Link
https://www.jstage.jst.go.jp/article/bpb/44/9/44_b21-00220/_pdf
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3. 3) Itoh T, Fairall L, Amin K, Inaba Y, Szanto A, Balint BL, Nagy L, Yamamoto K, Schwabe JW. Structural basis for the activation of PPARγ by oxidized fatty acids. Nat. Struct. Mol. Biol., 15, 924–931 (2008).
4. 4) Waku T, Shiraki T, Oyama T, Fujimoto Y, Maebara K, Kamiya N, Jingami H, Morikawa K. Structural insight into PPARγ activation through covalent modification with endogenous fatty acids. J. Mol. Biol., 385, 188–199 (2009).
5. 5) Franssen R, Vergeer M, Stroes ESG, Kastelein JJP. Combination statin-fibrate therapy: safety aspects. Diabetes Obes. Metab., 11, 89–94 (2009).
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