4LPH
Crystal structure of human FPPS in complex with CL03093
4LPH の概要
| エントリーDOI | 10.2210/pdb4lph/pdb |
| 関連するPDBエントリー | 4LPG |
| 分子名称 | Farnesyl pyrophosphate synthase, PHOSPHATE ION, ({[6-(4-methylphenyl)thieno[2,3-d]pyrimidin-4-yl]amino}methyl)phosphonic acid, ... (4 entities in total) |
| 機能のキーワード | transferase-transferase inhibitor complex, transferase/transferase inhibitor |
| 由来する生物種 | Homo sapiens (human) |
| 細胞内の位置 | Cytoplasm: P14324 |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 43575.27 |
| 構造登録者 | Park, J.,Leung, C.Y.,Tsantrizos, Y.S.,Berghuis, A.M. (登録日: 2013-07-16, 公開日: 2014-06-25, 最終更新日: 2023-09-20) |
| 主引用文献 | De Schutter, J.W.,Park, J.,Leung, C.Y.,Gormley, P.,Lin, Y.S.,Hu, Z.,Berghuis, A.M.,Poirier, J.,Tsantrizos, Y.S. Multistage screening reveals chameleon ligands of the human farnesyl pyrophosphate synthase: implications to drug discovery for neurodegenerative diseases. J.Med.Chem., 57:5764-5776, 2014 Cited by PubMed Abstract: Human farnesyl pyrophosphate synthase (hFPPS) is the gate-keeper of mammalian isoprenoids and the key target of bisphosphonate drugs. Bisphosphonates suffer from poor "drug-like" properties and are mainly effective in treating skeletal diseases. Recent investigations have implicated hFPPS in various nonskeletal diseases, including Alzheimer's disease (AD). Analysis of single nucleotide polymorphisms in the hFPPS gene and mRNA levels in autopsy-confirmed AD subjects was undertaken, and a genetic link between hFPPS and phosphorylated tau (P-Tau) levels in the human brain was identified. Elevated P-Tau levels are strongly implicated in AD progression. The development of nonbisphosphonate inhibitors can provide molecular tools for validating hFPPS as a therapeutic target for tauopathy-associated neurodegeneration. A multistage screening protocol led to the identification of a new monophosphonate chemotype that bind in an allosteric pocket of hFPPS. Optimization of these compounds could lead to human therapeutics that block tau metabolism and arrest the progression of neurodegeneration. PubMed: 24911527DOI: 10.1021/jm500629e 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.3 Å) |
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