3R02

The discovery of novel benzofuran-2-carboxylic acids as potent Pim-1 inhibitors

3R02 の概要

• エントリーDOI: 10.2210/pdb3r02/pdb
• 関連するPDBエントリー: 3R00 3R01 3R04
• 分子名称: Proto-oncogene serine/threonine-protein kinase pim-1, 7-[(cis-4-aminocyclohexyl)amino]-5-bromo-1-benzofuran-2-carboxylic acid, IMIDAZOLE, ... (4 entities in total)
• 機能のキーワード: kinase, pim1, inhibitor, transferase-transferase inhibitor complex, transferase/transferase inhibitor
• 由来する生物種: Homo sapiens (human)
• 細胞内の位置: Isoform 2: Cytoplasm. Isoform 1: Cell membrane: P11309
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 35041.56

構造登録者

Xiang, Y.,Hirth, B.,Asmussen, G.,Biemann, H.-P.,Good, A.,Fitzgerald, M.,Gladysheva, T.,Jancsics, K.,Liu, J.,Metz, M.,Papoulis, A.,Skerlj, R.,Stepp, D.J.,Wei, R.R. (登録日: 2011-03-07, 公開日: 2011-05-11, 最終更新日: 2024-02-21)

• 主引用文献: Xiang, Y.,Hirth, B.,Asmussen, G.,Biemann, H.P.,Bishop, K.A.,Good, A.,Fitzgerald, M.,Gladysheva, T.,Jain, A.,Jancsics, K.,Liu, J.,Metz, M.,Papoulis, A.,Skerlj, R.,Stepp, J.D.,Wei, R.R.; The discovery of novel benzofuran-2-carboxylic acids as potent Pim-1 inhibitors.; Bioorg.Med.Chem.Lett., 21:3050-3056, 2011; PubMed: 21507633; DOI: 10.1016/j.bmcl.2011.03.030

実験手法

X-RAY DIFFRACTION (1.95 Å)