8G8N
CTLA4 Fab with peptide
8G8N の概要
| エントリーDOI | 10.2210/pdb8g8n/pdb |
| 分子名称 | Fab heavy chain, Fab light chain, CYS-PRO-GLY-LYS-GLY-LEU-PRO-SER-CYS (3 entities in total) |
| 機能のキーワード | anti-ctla4 mab, immune system |
| 由来する生物種 | Homo sapiens (human) 詳細 |
| タンパク質・核酸の鎖数 | 18 |
| 化学式量合計 | 289156.69 |
| 構造登録者 | |
| 主引用文献 | Jenkins, K.A.,Park, M.,Pederzoli-Ribeil, M.,Eskiocak, U.,Johnson, P.,Guzman, W.,McLaughlin, M.,Moore-Lai, D.,O'Toole, C.,Liu, Z.,Nicholson, B.,Flesch, V.,Qiu, H.,Clackson, T.,O'Hagan, R.C.,Rodeck, U.,Karow, M.,O'Neil, J.,Williams, J.C. XTX101, a tumor-activated, Fc-enhanced anti-CTLA-4 monoclonal antibody, demonstrates tumor-growth inhibition and tumor-selective pharmacodynamics in mouse models of cancer. J Immunother Cancer, 11:-, 2023 Cited by PubMed Abstract: The clinical benefit of the anti-CTLA-4 monoclonal antibody (mAb) ipilimumab has been well established but limited by immune-related adverse events, especially when ipilimumab is used in combination with anti-PD-(L)1 mAb therapy. To overcome these limitations, we have developed XTX101, a tumor-activated, Fc-enhanced anti-CTLA-4 mAb. PubMed: 38164757DOI: 10.1136/jitc-2023-007785 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (3 Å) |
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