9F3W
| |
9BK1
| |
9BK8
| |
9BJY
| |
9F3Y
| |
9BK6
| |
9F48
| |
9F3X
| |
9F41
| Crystal structure of the NTD domain from S. cerevisia Niemann-Pick type C protein NCR1 with cholesterol bound | 分子名称: | (4S)-2-METHYL-2,4-PENTANEDIOL, CHOLESTEROL, DI(HYDROXYETHYL)ETHER, ... | 著者 | Nel, L, Olesen, E, Frain, K.M, Pedersen, B.P. | 登録日 | 2024-04-26 | 公開日 | 2024-05-29 | 実験手法 | X-RAY DIFFRACTION (2.64 Å) | 主引用文献 | Structural and biochemical analysis of ligand binding in yeast Niemann-Pick type C 1-related protein To Be Published
|
|
9F40
| Crystal structure of the NTD domain from S. cerevisia Niemann-Pick type C protein NCR1 with ergosterol bound | 分子名称: | ACETONITRILE, DI(HYDROXYETHYL)ETHER, ERGOSTEROL, ... | 著者 | Nel, L, Olesen, E, Frain, K.M, Pedersen, B.P. | 登録日 | 2024-04-26 | 公開日 | 2024-05-29 | 実験手法 | X-RAY DIFFRACTION (2.44 Å) | 主引用文献 | Structural and biochemical analysis of ligand binding in yeast Niemann-Pick type C 1-related protein To Be Published
|
|
9BK7
| |
9BK5
| |
8ZBE
| cryo-EM structure of the octreotide-bound SSTR5-Gi complex | 分子名称: | Beta-2 adrenergic receptor,Somatostatin receptor type 5,lgbit (fusion protein), Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, Guanine nucleotide-binding protein G(i) subunit alpha-1, ... | 著者 | Li, Y.G, Meng, X.Y, Yang, X.R, Ling, S.L, Shi, P, Tian, C.L, Yang, F. | 登録日 | 2024-04-26 | 公開日 | 2024-07-10 | 実験手法 | ELECTRON MICROSCOPY (3.24 Å) | 主引用文献 | Structural insights into somatostatin receptor 5 bound with cyclic peptides. Acta Pharmacol.Sin., 2024
|
|
9BK9
| |
8ZAH
| |
9BJA
| |
9F3E
| |
8ZAK
| |
9F3D
| |
9BJX
| GH5_4 endo-beta(1,3/1,4)-glucanase from Segatella copri | 分子名称: | 1,2-ETHANEDIOL, Cellulase (Glycosyl hydrolase family 5) | 著者 | Cordeiro, R.L, Golisch, B, Brumer, H, Van Petegem, F. | 登録日 | 2024-04-25 | 公開日 | 2024-10-09 | 実験手法 | X-RAY DIFFRACTION (1.6 Å) | 主引用文献 | The molecular basis of cereal mixed-linkage beta-glucan utilization by the human gut bacterium Segatella copri. J.Biol.Chem., 300, 2024
|
|
9BJ1
| Crystal structure of inhibitor GNE-6893 bound to HPK1 | 分子名称: | (4S,5R,7R,11aP)-10-{[(3R)-3-hydroxy-1-methyl-2-oxopyrrolidin-3-yl]ethynyl}-N~3~-methyl-6,7-dihydro-5H-5,7-methanoimidazo[2,1-a][2]benzazepine-2,3-dicarboxamide, (9S)-2-{[(6P)-8-amino-6-(5-amino-4-methylpyridin-3-yl)-7-fluoroisoquinolin-3-yl]amino}-6-methyl-5,6-dihydro-4H-pyrazolo[1,5-d][1,4]diazepin-7(8H)-one, 1,2-ETHANEDIOL, ... | 著者 | Kiefer, J.R, Tellis, J.C, Chan, B.K, Wang, W, Wu, P, Choo, E.F, Heffron, T.P, Wei, B, Siu, M. | 登録日 | 2024-04-24 | 公開日 | 2024-10-02 | 実験手法 | X-RAY DIFFRACTION (2.18 Å) | 主引用文献 | Discovery of GNE-6893, a Potent, Selective, Orally Bioavailable Small Molecule Inhibitor of HPK1. Acs Med.Chem.Lett., 15, 2024
|
|
9BIZ
| |
9BJ0
| |
9BIY
| |
9BIK
| Crystal structure of inhibitor 1 bound to HPK1 | 分子名称: | (1S,2S)-N-[(6P)-8-amino-6-(4-methylpyridin-3-yl)isoquinolin-3-yl]-2-cyanocyclopropane-1-carboxamide, 1,2-ETHANEDIOL, Mitogen-activated protein kinase kinase kinase kinase 1 | 著者 | Kiefer, J.T, Tellis, J.C, Chan, B.K, Wang, W, Wu, P, Siu, M, Heffron, T.P, Choo, E.F. | 登録日 | 2024-04-23 | 公開日 | 2024-10-02 | 実験手法 | X-RAY DIFFRACTION (2.25 Å) | 主引用文献 | Discovery of GNE-6893, a Potent, Selective, Orally Bioavailable Small Molecule Inhibitor of HPK1. Acs Med.Chem.Lett., 15, 2024
|
|