8H08
| |
8H07
| |
7LGI
| The haddock model of GDP KRas in complex with promazine using chemical shift perturbations and intermolecular NOEs | 分子名称: | GTPase KRas, GUANOSINE-5'-DIPHOSPHATE, MAGNESIUM ION, ... | 著者 | Wang, X, Gorfe, A.A, Putkey, J.A. | 登録日 | 2021-01-20 | 公開日 | 2021-07-21 | 最終更新日 | 2024-05-01 | 実験手法 | SOLUTION NMR | 主引用文献 | Antipsychotic phenothiazine drugs bind to KRAS in vitro. J.Biomol.Nmr, 75, 2021
|
|
7MIZ
| Atomic structure of cortical microtubule from Toxoplasma gondii | 分子名称: | GUANOSINE-5'-DIPHOSPHATE, GUANOSINE-5'-TRIPHOSPHATE, MAGNESIUM ION, ... | 著者 | Wang, X, Brown, A, Sibley, L.D, Zhang, R. | 登録日 | 2021-04-18 | 公開日 | 2021-06-02 | 最終更新日 | 2021-06-09 | 実験手法 | ELECTRON MICROSCOPY (3.4 Å) | 主引用文献 | Cryo-EM structure of cortical microtubules from human parasite Toxoplasma gondii identifies their microtubule inner proteins. Nat Commun, 12, 2021
|
|
7MQU
| The haddock model of GDP KRas in complex with promethazine using NMR chemical shift perturbations | 分子名称: | (2R)-N,N-dimethyl-1-(10H-phenothiazin-10-yl)propan-2-amine, GTPase KRas, GUANOSINE-5'-DIPHOSPHATE, ... | 著者 | Wang, X, Gorfe, A.A, Putkey, J.P. | 登録日 | 2021-05-06 | 公開日 | 2022-05-11 | 最終更新日 | 2024-05-15 | 実験手法 | SOLUTION NMR | 主引用文献 | Antipsychotic phenothiazine drugs bind to KRAS in vitro. J.Biomol.Nmr, 75, 2021
|
|
3HBF
| Structure of UGT78G1 complexed with myricetin and UDP | 分子名称: | 3,5,7-TRIHYDROXY-2-(3,4,5-TRIHYDROXYPHENYL)-4H-CHROMEN-4-ONE, Flavonoid 3-O-glucosyltransferase, URIDINE-5'-DIPHOSPHATE | 著者 | Wang, X, Modolo, L, Li, L, Dixon, R. | 登録日 | 2009-05-04 | 公開日 | 2009-09-01 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | 主引用文献 | Crystal structures of glycosyltransferase UGT78G1 reveal the molecular basis for glycosylation and deglycosylation of (iso)flavonoids. J.Mol.Biol., 392, 2009
|
|
3HBJ
| Structure of UGT78G1 complexed with UDP | 分子名称: | Flavonoid 3-O-glucosyltransferase, URIDINE-5'-DIPHOSPHATE | 著者 | Wang, X, Modolo, L, Li, L, Dixon, R. | 登録日 | 2009-05-04 | 公開日 | 2009-09-01 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | 主引用文献 | Crystal structures of glycosyltransferase UGT78G1 reveal the molecular basis for glycosylation and deglycosylation of (iso)flavonoids. J.Mol.Biol., 392, 2009
|
|
5K0K
| Crystal structure of the catalytic domain of the proto-oncogene tyrosine-protein kinase MER in complex with inhibitor UNC2434 | 分子名称: | 15-{4-[(4-methylpiperazin-1-yl)methyl]phenyl}-4,5,6,7,9,10,11,12-octahydro-2,16-(azenometheno)pyrrolo[2,1-d][1,3,5,9]te traazacyclotetradecin-8(3H)-one, CHLORIDE ION, MAGNESIUM ION, ... | 著者 | Wang, X, Liu, J, Zhang, W, Stashko, M.A, Nichols, J, DeRyckere, D, Miley, M.J, Norris-Drouin, J, Chen, Z, Machius, M, Wood, E, Graham, D.K, Earp, H.S, Graham, K, Kireev, D, Frye, S.V. | 登録日 | 2016-05-17 | 公開日 | 2017-01-11 | 最終更新日 | 2023-09-27 | 実験手法 | X-RAY DIFFRACTION (2.545 Å) | 主引用文献 | Design and Synthesis of Novel Macrocyclic Mer Tyrosine Kinase Inhibitors. ACS Med Chem Lett, 7, 2016
|
|
5ZUD
| Fit R10 Fab coordinates into the cryo-EM of EV71 in complex with D6 | 分子名称: | Capsid protein VP1, R10 ANTIBODY HEAVY CHAIN, R10 ANTIBODY LIGHT CHAIN, ... | 著者 | Wang, X, Zhu, L, Wang, N. | 登録日 | 2018-05-07 | 公開日 | 2019-12-25 | 最終更新日 | 2021-01-06 | 実験手法 | ELECTRON MICROSCOPY (4.9 Å) | 主引用文献 | Neutralization Mechanisms of Two Highly Potent Antibodies against Human Enterovirus 71. Mbio, 9, 2018
|
|
5ZUF
| Fit R10 Fab coordinates into the cryo-EM of EV71 in complex with A9 | 分子名称: | Capsid protein VP1, R10 ANTIBODY HEAVY CHAIN, R10 ANTIBODY LIGHT CHAIN, ... | 著者 | Wang, X, Zhu, L, Wang, N. | 登録日 | 2018-05-07 | 公開日 | 2019-12-25 | 最終更新日 | 2021-01-06 | 実験手法 | ELECTRON MICROSCOPY (6.8 Å) | 主引用文献 | Neutralization Mechanisms of Two Highly Potent Antibodies against Human Enterovirus 71. Mbio, 9, 2018
|
|
2P6V
| Structure of TAFH domain of the human TAF4 subunit of TFIID | 分子名称: | SULFATE ION, Transcription initiation factor TFIID subunit 4 | 著者 | Wang, X, Truckses, D.M, Takada, S, Matsumura, T, Tanese, N, Jacobson, R.H. | 登録日 | 2007-03-19 | 公開日 | 2007-05-15 | 最終更新日 | 2011-07-13 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Conserved region I of human coactivator TAF4 binds to a short hydrophobic motif present in transcriptional regulators. Proc.Natl.Acad.Sci.Usa, 104, 2007
|
|
4Y35
| |
4Y5E
| |
4Y4A
| |
4Y5B
| |
2P4H
| |
4Y3R
| |
4Y5C
| |
4Y45
| |
4Y5G
| |
4Y58
| |
4Y5K
| |
2GMG
| Solution NMR Structure of protein PF0610 from Pyrococcus furiosus, Northeast Structural Genomics Consortium Target PfG3 | 分子名称: | hypothetical protein Pf0610 | 著者 | Wang, X, Lee, H.S, Adams, M.W, Northeast Structural Genomics Consortium (NESG), Montelione, G.T, Prestegard, J.H. | 登録日 | 2006-04-06 | 公開日 | 2006-11-28 | 最終更新日 | 2024-05-01 | 実験手法 | SOLUTION NMR | 主引用文献 | PF0610, a novel winged helix-turn-helix variant possessing a rubredoxin-like Zn ribbon motif from the hyperthermophilic archaeon, Pyrococcus furiosus. Biochemistry, 46, 2007
|
|
5XEX
| Crystal structure of S.aureus PNPase catalytic domain | 分子名称: | DI(HYDROXYETHYL)ETHER, GLYCEROL, PYROPHOSPHATE, ... | 著者 | Wang, X, Zhang, X, Zang, J. | 登録日 | 2017-04-06 | 公開日 | 2017-10-18 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (2.2 Å) | 主引用文献 | Enolase binds to RnpA in competition with PNPase in Staphylococcus aureus FEBS Lett., 591, 2017
|
|
6UWL
| |