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-Structure paper
Title | Development of a Covalent Inhibitor of c-Jun N-Terminal Protein Kinase (JNK) 2/3 with Selectivity over JNK1. |
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Journal, issue, pages | J. Med. Chem., Vol. 66, Page 3356-3371, Year 2023 |
Publish date | Jun 15, 2021 (structure data deposition date) |
Authors | Lu, W. / Liu, Y. / Gao, Y. / Geng, Q. / Gurbani, D. / Li, L. / Ficarro, S.B. / Meyer, C.J. / Sinha, D. / You, I. ...Lu, W. / Liu, Y. / Gao, Y. / Geng, Q. / Gurbani, D. / Li, L. / Ficarro, S.B. / Meyer, C.J. / Sinha, D. / You, I. / Tse, J. / He, Z. / Ji, W. / Che, J. / Kim, A.Y. / Yu, T. / Wen, K. / Anderson, K.C. / Marto, J.A. / Westover, K.D. / Zhang, T. / Gray, N.S. |
External links | J. Med. Chem. / PubMed:36826833 |
Methods | X-ray diffraction |
Resolution | 1.69 - 2.072 Å |
Structure data | PDB-7n8t: PDB-8elc: |
Chemicals | ChemComp-AMP: ChemComp-P6G: ChemComp-HOH: ChemComp-Y56: |
Source |
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Keywords | TRANSFERASE / JNK2 / Mitogen-activated protein kinase 9 / AMP / TRANSFERASE/TRANSFERASE Inhibitor / YLIU2056 / Kinase Inhibitor / Structure-Based Drug Design / TRANSFERASE-Inhibitor complex / CELL CYCLE / TRANSFERASE-TRANSFERASE Inhibitor complex |