2R0D
| Crystal Structure of Autoinhibited Form of Grp1 Arf GTPase Exchange Factor | 分子名称: | Cytohesin-3, DI(HYDROXYETHYL)ETHER, INOSITOL-(1,3,4,5)-TETRAKISPHOSPHATE, ... | 著者 | DiNitto, J.P, Delprato, A, Gabe Lee, M.T, Cronin, T.C, Huang, S, Guilherme, A, Czech, M.P, Lambright, D.G. | 登録日 | 2007-08-18 | 公開日 | 2007-12-04 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (2.04 Å) | 主引用文献 | Structural Basis and Mechanism of Autoregulation in 3-Phosphoinositide-Dependent Grp1 Family Arf GTPase Exchange Factors. Mol.Cell, 28, 2007
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2LUL
| Solution NMR Structure of PH Domain of Tyrosine-protein kinase Tec from Homo sapiens, Northeast Structural Genomics Consortium (NESG) Target HR3504C | 分子名称: | Tyrosine-protein kinase Tec, ZINC ION | 著者 | Liu, G, Xiao, R, Janjua, H, Hamilton, K, Shastry, R, Kohan, E, Acton, T.B, Everett, J.K, Lee, H, Pederson, K, Huang, Y.J, Montelione, G.T, Northeast Structural Genomics Consortium (NESG) | 登録日 | 2012-06-15 | 公開日 | 2012-08-15 | 最終更新日 | 2024-05-15 | 実験手法 | SOLUTION NMR | 主引用文献 | Solution NMR Structure of PH Domain of Tyrosine-protein kinase Tec from Homo sapiens, Northeast Structural Genomics Consortium (NESG) Target HR3504C To be Published
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4GMV
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4GZU
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4H6Y
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4GN1
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4H8S
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2Z0O
| Crystal structure of APPL1-BAR-PH domain | 分子名称: | DCC-interacting protein 13-alpha | 著者 | Murayama, K, Kato-Murayama, M, Terada, T, Shirouzu, M, Yokoyama, S, RIKEN Structural Genomics/Proteomics Initiative (RSGI) | 登録日 | 2007-05-07 | 公開日 | 2008-05-13 | 最終更新日 | 2011-07-13 | 実験手法 | X-RAY DIFFRACTION (2.58 Å) | 主引用文献 | Crystal structure of APPL1-BAR-PH domain To be Published
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2Z0P
| Crystal structure of PH domain of Bruton's tyrosine kinase | 分子名称: | (2R)-3-{[(S)-{[(2S,3R,5S,6S)-2,6-DIHYDROXY-3,4,5-TRIS(PHOSPHONOOXY)CYCLOHEXYL]OXY}(HYDROXY)PHOSPHORYL]OXY}-2-(1-HYDROXY BUTOXY)PROPYL BUTYRATE, Tyrosine-protein kinase BTK, ZINC ION | 著者 | Murayama, K, Kato-Murayama, M, Mishima, C, Shirouzu, M, Yokoyama, S, RIKEN Structural Genomics/Proteomics Initiative (RSGI) | 登録日 | 2007-05-07 | 公開日 | 2008-05-13 | 最終更新日 | 2023-11-01 | 実験手法 | X-RAY DIFFRACTION (2.58 Å) | 主引用文献 | Crystal structure of the Bruton's tyrosine kinase PH domain with phosphatidylinositol Biochem.Biophys.Res.Commun., 377, 2008
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2YS3
| Solution structure of the PH domain of Kindlin-3 from human | 分子名称: | Unc-112-related protein 2 | 著者 | Li, H, Sato, M, Koshiba, S, Watanabe, S, Harada, T, Kigawa, T, Yokoyama, S, RIKEN Structural Genomics/Proteomics Initiative (RSGI) | 登録日 | 2007-04-03 | 公開日 | 2007-10-09 | 最終更新日 | 2024-05-29 | 実験手法 | SOLUTION NMR | 主引用文献 | Solution structure of the PH domain of Kindlin-3 from human To be Published
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4K2O
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4K2P
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3ZYS
| Human dynamin 1 deltaPRD polymer stabilized with GMPPCP | 分子名称: | DYNAMIN-1, INTERFERON-INDUCED GTP-BINDING PROTEIN MX1 | 著者 | Chappie, J.S, Mears, J.A, Fang, S, Leonard, M, Schmid, S.L, Milligan, R.A, Hinshaw, J.E, Dyda, F. | 登録日 | 2011-08-24 | 公開日 | 2011-10-12 | 最終更新日 | 2024-05-08 | 実験手法 | ELECTRON MICROSCOPY (12.2 Å) | 主引用文献 | A Pseudoatomic Model of the Dynamin Polymer Identifies a Hydrolysis-Dependent Powerstroke. Cell(Cambridge,Mass.), 147, 2011
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3ZVR
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4BBK
| Structural and functional characterisation of the kindlin-1 pleckstrin homology domain | 分子名称: | FERMITIN FAMILY HOMOLOG 1, GLYCEROL | 著者 | Yates, L.A, Lumb, C.N, Brahme, N.N, Zalyte, R, Bird, L.E, De Colibus, L, Owens, R.J, Calderwood, D.A, Sansom, M.S.P, Gilbert, R.J.C. | 登録日 | 2012-09-25 | 公開日 | 2012-11-14 | 最終更新日 | 2023-12-20 | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | 主引用文献 | Structural and Functional Characterisation of the Kindlin-1 Pleckstrin Homology Domain J.Biol.Chem., 287, 2012
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8SZ4
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8SZ7
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8T0R
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8SXZ
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8T0K
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8SZ8
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8TYM
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8TYN
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2ELB
| Crystal Structure of the BAR-PH domain of human APPL1 | 分子名称: | Adapter protein containing PH domain, PTB domain and leucine zipper motif 1 | 著者 | Li, J, Mao, X, Dong, L.Q, Liu, F, Tong, L. | 登録日 | 2007-03-27 | 公開日 | 2007-05-29 | 最終更新日 | 2011-07-13 | 実験手法 | X-RAY DIFFRACTION (2.6 Å) | 主引用文献 | Crystal Structures of the BAR-PH and PTB Domains of Human APPL1 Structure, 15, 2007
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9C1W
| Structure of AKT2 with compound 3 | 分子名称: | 1,2-ETHANEDIOL, 4-{2-[({4-[(2P)-2-(2-aminopyridin-3-yl)-5-phenyl-3H-imidazo[4,5-b]pyridin-3-yl]phenyl}methyl)amino]ethyl}-2-hydroxybenzaldehyde, RAC-beta serine/threonine-protein kinase | 著者 | Craven, G.B, Ma, X, Taunton, J. | 登録日 | 2024-05-29 | 公開日 | 2024-09-04 | 最終更新日 | 2024-10-16 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Mutant-selective AKT1 inhibitors via lysine targeting and neo-zinc chelation To Be Published
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