4WVS
Crystal structure of XIAP-BIR2 domain complexed with (S)-3-(4-methoxyphenyl)-2-((S)-2-((S)-1-((S)-2-((S)-2-(methylamino)propanamido)pent-4-ynoyl)pyrrolidine-2-carboxamido)-3-phenylpropanamido)propanoic acid
4WVS の概要
| エントリーDOI | 10.2210/pdb4wvs/pdb |
| 関連するPDBエントリー | 4WVT 4WVU |
| 分子名称 | E3 ubiquitin-protein ligase XIAP, 3,11-DIFLUORO-6,8,13-TRIMETHYL-8H-QUINO[4,3,2-KL]ACRIDIN-13-IUM, ZINC ION, ... (6 entities in total) |
| 機能のキーワード | iap, xiap-bir2, apoptosis |
| 由来する生物種 | Homo sapiens (Human) 詳細 |
| 細胞内の位置 | Cytoplasm: P98170 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 12481.10 |
| 構造登録者 | |
| 主引用文献 | Seigal, B.A.,Connors, W.H.,Fraley, A.,Borzilleri, R.M.,Carter, P.H.,Emanuel, S.L.,Fargnoli, J.,Kim, K.,Lei, M.,Naglich, J.G.,Pokross, M.E.,Posy, S.L.,Shen, H.,Surti, N.,Talbott, R.,Zhang, Y.,Terrett, N.K. The Discovery of Macrocyclic XIAP Antagonists from a DNA-Programmed Chemistry Library, and Their Optimization To Give Lead Compounds with in Vivo Antitumor Activity. J.Med.Chem., 58:2855-2861, 2015 Cited by PubMed Abstract: Affinity selection screening of macrocycle libraries derived from DNA-programmed chemistry identified XIAP BIR2 and BIR3 domain inhibitors that displace bound pro-apoptotic caspases. X-ray cocrystal structures of key compounds with XIAP BIR2 suggested potency-enhancing structural modifications. Optimization of dimeric macrocycles with similar affinity for both domains were potent pro-apoptotic agents in cancer cell lines and efficacious in shrinking tumors in a mouse xenograft model. PubMed: 25695766DOI: 10.1021/jm501892g 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.09 Å) |
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