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4CBT
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BU of 4cbt by Molmil
Design, synthesis, and biological evaluation of potent and selective Class IIa HDAC inhibitors as a potential therapy for Huntington's disease
分子名称: (1R,2R,3R)-2-[4-(5-fluoranylpyrimidin-2-yl)phenyl]-N-oxidanyl-3-phenyl-cyclopropane-1-carboxamide, HISTONE DEACETYLASE 4, ZINC ION
著者Burli, R.W, Luckhurst, C.A, Aziz, O, Matthews, K.L, Yates, D, Lyons, K.A, Beconi, M, McAllister, G, Breccia, P, Stott, A.J, Penrose, S.D, Wall, M, Lamers, M, Leonard, P, Mueller, I, Richardson, C.M, Jarvis, R, Stones, L, Hughes, S, Wishart, G, Haughan, A.F, O'Connell, C, Mead, T, McNeil, H, Vann, J, Mangette, J, Maillard, M, Beaumont, V, Munoz-Sanjuan, I, Dominguez, C.
登録日2013-10-16
公開日2013-12-11
最終更新日2024-05-08
実験手法X-RAY DIFFRACTION (3.03 Å)
主引用文献Design, synthesis, and biological evaluation of potent and selective class IIa histone deacetylase (HDAC) inhibitors as a potential therapy for Huntington's disease.
J. Med. Chem., 56, 2013
4CBY
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BU of 4cby by Molmil
Design, synthesis, and biological evaluation of potent and selective Class IIa HDAC inhibitors as a potential therapy for Huntington's disease
分子名称: (1R,2R,3R)-2-[4-(1,3-oxazol-5-yl)phenyl]-N-oxidanyl-3-phenyl-cyclopropane-1-carboxamide, HISTONE DEACETYLASE 4, SODIUM ION, ...
著者Burli, R.W, Luckhurst, C.A, Aziz, O, Matthews, K.L, Yates, D, Lyons, K.A, Beconi, M, McAllister, G, Breccia, P, Stott, A.J, Penrose, S.D, Wall, M, Lamers, M, Leonard, P, Mueller, I, Richardson, C.M, Jarvis, R, Stones, L, Hughes, S, Wishart, G, Haughan, A.F, O'Connell, C, Mead, T, McNeil, H, Vann, J, Mangette, J, Maillard, M, Beaumont, V, Munoz-Sanjuan, I, Dominguez, C.
登録日2013-10-17
公開日2013-12-11
最終更新日2024-05-08
実験手法X-RAY DIFFRACTION (2.72 Å)
主引用文献Design, synthesis, and biological evaluation of potent and selective class IIa histone deacetylase (HDAC) inhibitors as a potential therapy for Huntington's disease.
J. Med. Chem., 56, 2013
6FYZ
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BU of 6fyz by Molmil
Development and characterization of a CNS-penetrant benzhydryl hydroxamic acid class IIa histone deacetylase inhibitor
分子名称: (2~{S})-2-(2-fluorophenyl)-2-[4-(2-methylpyrimidin-5-yl)phenyl]-~{N}-oxidanyl-ethanamide, Histone deacetylase 4, SODIUM ION, ...
著者Luckhurst, C.A, Maillard, M.C, Dominguez, C.
登録日2018-03-13
公開日2018-12-05
最終更新日2024-01-17
実験手法X-RAY DIFFRACTION (2.15 Å)
主引用文献Development and characterization of a CNS-penetrant benzhydryl hydroxamic acid class IIa histone deacetylase inhibitor.
Bioorg. Med. Chem. Lett., 29, 2019
7P6N
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BU of 7p6n by Molmil
ROCK2 IN COMPLEX WITH COMPOUND 12
分子名称: Rho-associated protein kinase 2, ~{N}-[(1~{R})-1-(3-methoxyphenyl)ethyl]-4-pyridin-4-yl-piperidine-1-carboxamide
著者Maillard, M.C.
登録日2021-07-16
公開日2022-07-27
最終更新日2024-06-19
実験手法X-RAY DIFFRACTION (3 Å)
主引用文献Identification of a Potent, Selective, and Brain-Penetrant Rho Kinase Inhibitor and its Activity in a Mouse Model of Huntington's Disease.
J.Med.Chem., 65, 2022
6DT6
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BU of 6dt6 by Molmil
Crystal Structure of the YopH PTP1B Chimera 3 PTPase bound to vanadate
分子名称: Targeted effector protein, VANADATE ION
著者Morales, Y, Johnson, S.J, Hengge, A.C.
登録日2018-06-15
公開日2018-08-29
最終更新日2023-10-11
実験手法X-RAY DIFFRACTION (2.101 Å)
主引用文献A YopH PTP1B Chimera Shows the Importance of the WPD-Loop Sequence to the Activity, Structure, and Dynamics of Protein Tyrosine Phosphatases.
Biochemistry, 57, 2018
6DRB
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BU of 6drb by Molmil
Crystal Structure of the YopH PTP1B WPD loop Chimera 3 PTPase bound to tungstate
分子名称: TUNGSTATE(VI)ION, Targeted effector protein
著者Morales, Y, Johnson, S.J, Hengge, A.C.
登録日2018-06-11
公開日2018-08-29
最終更新日2023-10-11
実験手法X-RAY DIFFRACTION (2.745 Å)
主引用文献A YopH PTP1B Chimera Shows the Importance of the WPD-Loop Sequence to the Activity, Structure, and Dynamics of Protein Tyrosine Phosphatases.
Biochemistry, 57, 2018
6DR1
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BU of 6dr1 by Molmil
YopH PTP1B Chimera 2 PTPase
分子名称: Targeted effector protein
著者Morales, Y, Johnson, S.J, Hengge, A.C.
登録日2018-06-11
公開日2018-08-29
最終更新日2023-10-11
実験手法X-RAY DIFFRACTION (2.5 Å)
主引用文献A YopH PTP1B Chimera Shows the Importance of the WPD-Loop Sequence to the Activity, Structure, and Dynamics of Protein Tyrosine Phosphatases.
Biochemistry, 57, 2018
6DR7
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BU of 6dr7 by Molmil
YopH PTP1B WPD loop Chimera 2 PTPase bound to vanadate
分子名称: ACETATE ION, Targeted effector protein, VANADATE ION
著者Moise, G, Morales, Y, Johnson, S.J, Hengge, A.C.
登録日2018-06-11
公開日2018-08-29
最終更新日2023-10-11
実験手法X-RAY DIFFRACTION (1.849 Å)
主引用文献A YopH PTP1B Chimera Shows the Importance of the WPD-Loop Sequence to the Activity, Structure, and Dynamics of Protein Tyrosine Phosphatases.
Biochemistry, 57, 2018
6DR9
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BU of 6dr9 by Molmil
Crystal Structure of the YopH PTP1B Chimera 3 PTPase apo form
分子名称: Targeted effector protein
著者Morales, Y, Johnson, S.J, Hengge, A.C.
登録日2018-06-11
公開日2018-08-29
最終更新日2023-10-11
実験手法X-RAY DIFFRACTION (1.945 Å)
主引用文献A YopH PTP1B Chimera Shows the Importance of the WPD-Loop Sequence to the Activity, Structure, and Dynamics of Protein Tyrosine Phosphatases.
Biochemistry, 57, 2018

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件を2024-10-30に公開中

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