8V52
Crystal structure of 2A10 Fab bound to Human TGF-beta3
8V52 の概要
| エントリーDOI | 10.2210/pdb8v52/pdb |
| 分子名称 | Transforming growth factor beta-3, 2A10 Fab Light chain, 2A10 Fab Heavy Chain, ... (4 entities in total) |
| 機能のキーワード | tgf beta, 2a10, complex, fab, cytokine, cytokine-immune system complex, cytokine/immune system |
| 由来する生物種 | Homo sapiens (human) 詳細 |
| タンパク質・核酸の鎖数 | 6 |
| 化学式量合計 | 121433.79 |
| 構造登録者 | |
| 主引用文献 | Sun, T.,Vander Heiden, J.A.,Gao, X.,Yin, J.,Uttarwar, S.,Liang, W.C.,Jia, G.,Yadav, R.,Huang, Z.,Mitra, M.,Halpern, W.,Bender, H.S.,Brightbill, H.D.,Wu, Y.,Lupardus, P.,Ramalingam, T.,Arron, J.R. Isoform-selective TGF-beta 3 inhibition for systemic sclerosis. Med, 5:132-147.e7, 2024 Cited by PubMed Abstract: Transforming growth factor β (TGF-β) is implicated as a key mediator of pathological fibrosis, but its pleiotropic activity in a range of homeostatic functions presents challenges to its safe and effective therapeutic targeting. There are three isoforms of TGF-β, TGF-β1, TGF-β2, and TGF-β3, which bind to a common receptor complex composed of TGF-βR1 and TGF-βR2 to induce similar intracellular signals in vitro. We have recently shown that the cellular expression patterns and activation thresholds of TGF-β2 and TGF-β3 are distinct from those of TGF-β1 and that selective short-term TGF-β2 and TGF-β3 inhibition can attenuate fibrosis in vivo without promoting excessive inflammation. Isoform-selective inhibition of TGF-β may therefore provide a therapeutic opportunity for patients with chronic fibrotic disorders. PubMed: 38272035DOI: 10.1016/j.medj.2023.12.011 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.5 Å) |
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