8H4R
The Crystal Structure of CDK3 and CyclinE1 Complex with Dinaciclib from Biortus
8H4R の概要
| エントリーDOI | 10.2210/pdb8h4r/pdb |
| 分子名称 | Glutathione S-transferase class-mu 26 kDa isozyme,Cyclin-dependent kinase 3, G1/S-specific cyclin-E1, 3-[({3-ethyl-5-[(2S)-2-(2-hydroxyethyl)piperidin-1-yl]pyrazolo[1,5-a]pyrimidin-7-yl}amino)methyl]-1-hydroxypyridinium, ... (7 entities in total) |
| 機能のキーワード | complex, cell cycle |
| 由来する生物種 | Schistosoma japonicum (Blood fluke) 詳細 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 98848.06 |
| 構造登録者 | |
| 主引用文献 | Gui, W.,Hang, Y.,Cheng, W.,Gao, M.,Wu, J.,Ouyang, Z. Structural basis of CDK3 activation by cyclin E1 and inhibition by dinaciclib. Biochem.Biophys.Res.Commun., 662:126-134, 2023 Cited by PubMed Abstract: Cell cycle transitions are controlled by multiple cell cycle regulators, especially CDKs. Several CDKs, including CDK1-4 and CDK6, promote cell cycle progression directly. Among them, CDK3 is critically important because it triggers the transitions of G0 to G1 and G1 to S phase through binding to cyclin C and cyclin E1, respectively. In contrast to its highly related homologs, the molecular basis of CDK3 activation remains elusive due to the lack of structural information of CDK3, particularly in cyclin bound form. Here we report the crystal structure of CDK3 in complex with cyclin E1 at 2.25 Å resolution. CDK3 resembles CDK2 in that both adopt a similar fold and bind cyclin E1 in a similar way. The structural discrepancy between CDK3 and CDK2 may reflect their substrate specificity. Profiling a panel of CDK inhibitors reveals that dinaciclib inhibits CDK3-cyclin E1 potently and specifically. The structure of CDK3-cyclin E1 bound to dinaciclib reveals the inhibitory mechanism. The structural and biochemical results uncover the mechanism of CDK3 activation by cyclin E1 and lays a foundation for structural-based drug design. PubMed: 37104883DOI: 10.1016/j.bbrc.2023.04.026 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.75 Å) |
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