4KD1

CDK2 in complex with Dinaciclib

4KD1 の概要

• エントリーDOI: 10.2210/pdb4kd1/pdb
• 分子名称: Cyclin-dependent kinase 2, 1,2-ETHANEDIOL, 3-[({3-ethyl-5-[(2S)-2-(2-hydroxyethyl)piperidin-1-yl]pyrazolo[1,5-a]pyrimidin-7-yl}amino)methyl]-1-hydroxypyridinium, ... (4 entities in total)
• 機能のキーワード: protein kinase, dinaciclib, transferase-transferase, cell cycle-inhibitor complex, cell cycle/inhibitor
• 由来する生物種: Homo sapiens (human)
• 細胞内の位置: Cytoplasm, cytoskeleton, microtubule organizing center, centrosome: P24941
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 34436.05

構造登録者

Martin, M.P.,Schonbrunn, E. (登録日: 2013-04-24, 公開日: 2013-09-18, 最終更新日: 2023-09-20)

主引用文献

Martin, M.P.,Olesen, S.H.,Georg, G.I.,Schonbrunn, E.
Cyclin-dependent kinase inhibitor dinaciclib interacts with the acetyl-lysine recognition site of bromodomains.
Acs Chem.Biol., 8:2360-2365, 2013

PubMed Abstract: Bromodomain-containing proteins are considered atypical kinases, but their potential to interact with kinase inhibitors is unknown. Dinaciclib is a potent inhibitor of cyclin-dependent kinases (CDKs), which recently advanced to Phase III clinical trials for the treatment of leukemia. We determined the crystal structure of dinaciclib in complex with CDK2 at 1.7 Å resolution, revealing an elaborate network of binding interactions in the ATP site, which explains the extraordinary potency and selectivity of this inhibitor. Remarkably, dinaciclib also interacted with the acetyl-lysine recognition site of the bromodomain testis-specific protein BRDT, a member of the BET family of bromodomains. The binding mode of dinaciclib to BRDT at 2.0 Å resolution suggests that general kinase inhibitors ("hinge binders") possess a previously unrecognized potential to act as protein-protein inhibitors of bromodomains. The findings may provide a new structural framework for the design of next-generation bromodomain inhibitors using the vast chemical space of kinase inhibitors.

PubMed: 24007471
DOI: 10.1021/cb4003283

実験手法

X-RAY DIFFRACTION (1.7 Å)