8F48
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4YGX
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4YH1
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4YGY
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6DU3
| Structure of Scp1 D96N bound to REST-pS861/4 peptide | 分子名称: | Carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1, MAGNESIUM ION, REST-pS861 | 著者 | Burkholder, N.T, Mayfield, J.E, Yu, X, Irani, S, Arce, D.K, Jiang, F, Matthews, W, Xue, Y, Zhang, Y.J. | 登録日 | 2018-06-19 | 公開日 | 2018-09-26 | 最終更新日 | 2020-01-01 | 実験手法 | X-RAY DIFFRACTION (2.58 Å) | 主引用文献 | Phosphatase activity of small C-terminal domain phosphatase 1 (SCP1) controls the stability of the key neuronal regulator RE1-silencing transcription factor (REST). J. Biol. Chem., 293, 2018
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6DU2
| Structure of Scp1 D96N bound to REST-pS861/4 peptide | 分子名称: | MAGNESIUM ION, REST-pS861/4, carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1 isoform X2 | 著者 | Burkholder, N.T, Mayfield, J.E, Yu, X, Irani, S, Arce, D.K, Jiang, F, Matthews, W, Xue, Y, Zhang, Y.J. | 登録日 | 2018-06-19 | 公開日 | 2018-09-26 | 最終更新日 | 2024-10-16 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Phosphatase activity of small C-terminal domain phosphatase 1 (SCP1) controls the stability of the key neuronal regulator RE1-silencing transcription factor (REST). J. Biol. Chem., 293, 2018
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6K0J
| The co-crystal structure of DYRK2 with a small molecule inhibitor | 分子名称: | 3-(2,7-dimethoxyacridin-9-yl)sulfanylpropan-1-amine, Dual specificity tyrosine-phosphorylation-regulated kinase 2 | 著者 | Tiantian, W, Xiao, J. | 登録日 | 2019-05-06 | 公開日 | 2019-11-20 | 最終更新日 | 2019-12-18 | 実験手法 | X-RAY DIFFRACTION (2.352 Å) | 主引用文献 | Inhibition of dual-specificity tyrosine phosphorylation-regulated kinase 2 perturbs 26S proteasome-addicted neoplastic progression. Proc.Natl.Acad.Sci.USA, 116, 2019
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5ZTN
| The crystal structure of human DYRK2 in complex with Curcumin | 分子名称: | (1Z,4Z,6E)-5-hydroxy-1,7-bis(4-hydroxy-3-methoxyphenyl)hepta-1,4,6-trien-3-one, Dual specificity tyrosine-phosphorylation-regulated kinase 2 | 著者 | Ji, C.G, Xiao, J.Y. | 登録日 | 2018-05-04 | 公開日 | 2018-07-18 | 最終更新日 | 2024-10-16 | 実験手法 | X-RAY DIFFRACTION (2.496 Å) | 主引用文献 | Ancient drug curcumin impedes 26S proteasome activity by direct inhibition of dual-specificity tyrosine-regulated kinase 2. Proc. Natl. Acad. Sci. U.S.A., 115, 2018
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