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9H7C

Human Transthyretin in Complex with 4-(1H-imidazol-1-yl)phenol

9H7C の概要
エントリーDOI10.2210/pdb9h7c/pdb
分子名称Transthyretin, CALCIUM ION, 4-(1H-IMIDAZOL-1-YL)PHENOL, ... (4 entities in total)
機能のキーワードamyloidosis, retinol, thyroxine, rbp, transport protein
由来する生物種Homo sapiens (human)
タンパク質・核酸の鎖数2
化学式量合計27955.22
構造登録者
Chen, W. (登録日: 2024-10-27, 公開日: 2025-03-12, 最終更新日: 2025-05-28)
主引用文献Chen, W.
Fragment-based drug discovery for transthyretin kinetic stabilisers using a novel capillary zone electrophoresis method.
Plos One, 20:e0323816-e0323816, 2025
Cited by
PubMed Abstract: A Capillary Zone Electrophoresis (CZE) fragment screening methodology was developed and applied to the human plasma protein Transthyretin (TTR), normally soluble, but could misfold and aggregate, causing amyloidosis. Termed Free Probe Peak Height Restoration (FPPHR), it monitors changes in the level of free ligand known to bind TTR (the Probe Ligand) in the presence of competing fragments. 129 fragments were screened, 12 of the 16 initial hits (12.4% hit rate) were co-crystallised with TTR, 11 were found at the binding site (92% confirmation rate). Subsequent analogue screens have identified a novel TTR-binding scaffold 4-(3H-pyrazol-4-yl)quinoline and its derived compounds were further studied by crystallography, circular dichroism (CD), isothermal titration calorimetry (ITC) and radiolabelled 125I-Thyroxine displacement assay in neat plasma. Two lead molecules had similar ITC Kd and 125I-Thyroxine displacement IC50 values to that of Tafamidis, adding another potential pipeline for transthyretin amyloidosis. The methodology is reproducible, procedurally simple, automatable, label-free without target immobilisation, non-fluorescence based and site-specific with low false positive rate, which could be applicable to fragment screening of many drug targets.
PubMed: 40367241
DOI: 10.1371/journal.pone.0323816
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.27 Å)
構造検証レポート
Validation report summary of 9h7c
検証レポート(詳細版)ダウンロードをダウンロード

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件を2025-06-25に公開中

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