5ACB

Crystal Structure of the Human Cdk12-Cyclink Complex

5ACB の概要

• エントリーDOI: 10.2210/pdb5acb/pdb
• 分子名称: CYCLIN-K, CYCLIN-DEPENDENT KINASE 12, N-[4-[(3R)-3-[[5-chloranyl-4-(1H-indol-3-yl)pyrimidin-2-yl]amino]piperidin-1-yl]carbonylphenyl]-4-(dimethylamino)butanamide (3 entities in total)
• 機能のキーワード: transferase
• 由来する生物種: HOMO SAPIENS (HUMAN); 詳細
• 細胞内の位置: Nucleus: Q9NYV4
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 141446.32

構造登録者

Dixon Clarke, S.E.,Elkins, J.M.,Pike, A.C.W.,Mackenzie, A.,Goubin, S.,Strain-Damerell, C.,Mahajan, P.,Tallant, C.,Chalk, R.,Wiggers, H.,Kopec, J.,Fitzpatrick, F.,Burgess-Brown, N.,Carpenter, E.P.,von Delft, F.,Arrowsmith, C.H.,Edwards, A.M.,Bountra, C.,Bullock, A. (登録日: 2015-08-14, 公開日: 2016-06-15, 最終更新日: 2024-11-13)

主引用文献

Zhang, T.,Kwiatkowski, N.,Olson, C.M.,Dixon-Clarke, S.E.,Abraham, B.J.,Greifenberg, A.K.,Ficarro, S.B.,Elkins, J.M.,Liang, Y.,Hannett, N.M.,Manz, T.,Hao, M.,Bartkowiak, B.,Greenleaf, A.L.,Marto, J.A.,Geyer, M.,Bullock, A.N.,Young, R.A.,Gray, N.S.
Covalent Targeting of Remote Cysteine Residues to Develop Cdk12 and Cdk13 Inhibitors.
Nat.Chem.Biol., 12:876-, 2016

PubMed Abstract: Cyclin-dependent kinases 12 and 13 (CDK12 and CDK13) play critical roles in the regulation of gene transcription. However, the absence of CDK12 and CDK13 inhibitors has hindered the ability to investigate the consequences of their inhibition in healthy cells and cancer cells. Here we describe the rational design of a first-in-class CDK12 and CDK13 covalent inhibitor, THZ531. Co-crystallization of THZ531 with CDK12-cyclin K indicates that THZ531 irreversibly targets a cysteine located outside the kinase domain. THZ531 causes a loss of gene expression with concurrent loss of elongating and hyperphosphorylated RNA polymerase II. In particular, THZ531 substantially decreases the expression of DNA damage response genes and key super-enhancer-associated transcription factor genes. Coincident with transcriptional perturbation, THZ531 dramatically induced apoptotic cell death. Small molecules capable of specifically targeting CDK12 and CDK13 may thus help identify cancer subtypes that are particularly dependent on their kinase activities.

PubMed: 27571479
DOI: 10.1038/NCHEMBIO.2166

実験手法

X-RAY DIFFRACTION (2.7 Å)