8I8C
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8I8B
| Outer shell and inner layer structures of Autographa californica multiple nucleopolyhedrovirus (AcMNPV) | 分子名称: | 38K, AcOrf-109 peptide, Early 49 Daa protein, ... | 著者 | Jia, X, Gao, Y, Zhang, Q. | 登録日 | 2023-02-03 | 公開日 | 2023-12-13 | 最終更新日 | 2024-10-16 | 実験手法 | ELECTRON MICROSCOPY (4.31 Å) | 主引用文献 | Architecture of the baculovirus nucleocapsid revealed by cryo-EM. Nat Commun, 14, 2023
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8WHK
| Crystal structure of CLASP2 in complex with LL5beta | 分子名称: | CHLORIDE ION, CLIP-associating protein 2, Pleckstrin homology-like domain family B member 2 | 著者 | Jia, X, Wei, Z. | 登録日 | 2023-09-23 | 公開日 | 2024-08-28 | 実験手法 | X-RAY DIFFRACTION (2.401 Å) | 主引用文献 | CLASP-mediated competitive binding in protein condensates directs microtubule growth. Nat Commun, 15, 2024
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8WHJ
| Crystal structure of CLASP2 TOG4 fused with LL5beta | 分子名称: | CHLORIDE ION, CLIP-associating protein 2,Pleckstrin homology-like domain family B member 2, DI(HYDROXYETHYL)ETHER | 著者 | Jia, X, Wei, Z. | 登録日 | 2023-09-23 | 公開日 | 2024-08-28 | 実験手法 | X-RAY DIFFRACTION (1.4 Å) | 主引用文献 | CLASP-mediated competitive binding in protein condensates directs microtubule growth. Nat Commun, 15, 2024
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8WHL
| Crystal structure of CLASP2 in complex with CENP-E | 分子名称: | ACETATE ION, CLIP-associating protein 2, Centromere-associated protein E, ... | 著者 | Jia, X, Wei, Z. | 登録日 | 2023-09-23 | 公開日 | 2024-08-28 | 実験手法 | X-RAY DIFFRACTION (3.2 Å) | 主引用文献 | CLASP-mediated competitive binding in protein condensates directs microtubule growth. Nat Commun, 15, 2024
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8WHM
| Crystal structure of the ELKS2/LL5beta complex | 分子名称: | ERC protein 2, Pleckstrin homology-like domain family B member 2 | 著者 | Jia, X, Wei, Z. | 登録日 | 2023-09-23 | 公開日 | 2024-08-28 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | CLASP-mediated competitive binding in protein condensates directs microtubule growth. Nat Commun, 15, 2024
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8W4F
| SARS-CoV-2 spike protein in complex with a trivalent nanobody | 分子名称: | Spike glycoprotein, Tribody | 著者 | Jiang, X.Y, Qian, J.Q, Zhu, H.X, Qin, Q, Huang, Q. | 登録日 | 2023-08-24 | 公開日 | 2024-07-24 | 実験手法 | ELECTRON MICROSCOPY (4.2 Å) | 主引用文献 | Structure-guided design of a trivalent nanobody cluster targeting SARS-CoV-2 spike protein. Int.J.Biol.Macromol., 256, 2024
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5GXB
| crystal structure of a LacY/Nanobody complex | 分子名称: | Lactose permease, nanobody | 著者 | Jiang, X, Wu, J.P, Yan, N, Kaback, H.R. | 登録日 | 2016-09-16 | 公開日 | 2016-10-26 | 最終更新日 | 2024-05-22 | 実験手法 | X-RAY DIFFRACTION (3.3 Å) | 主引用文献 | Crystal structure of a LacY-nanobody complex in a periplasmic-open conformation. Proc.Natl.Acad.Sci.USA, 113, 2016
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4G9Z
| Lassa nucleoprotein with dsRNA reveals novel mechanism for immune suppression | 分子名称: | Nucleoprotein, RNA (5'-R(P*GP*CP*CP*C)-3'), RNA (5'-R(P*GP*GP*GP*C)-3'), ... | 著者 | Jiang, X, Huang, Q, Wang, W, Dong, H, Ly, H, Liang, Y, Dong, C, Scottish Structural Proteomics Facility (SSPF) | 登録日 | 2012-07-24 | 公開日 | 2013-04-03 | 最終更新日 | 2024-02-28 | 実験手法 | X-RAY DIFFRACTION (2.03 Å) | 主引用文献 | Structures of Arenaviral Nucleoproteins with Triphosphate dsRNA Reveal a Unique Mechanism of Immune Suppression. J.Biol.Chem., 288, 2013
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4NKI
| Crystal structure of a Fab | 分子名称: | 1,2-ETHANEDIOL, Fab heavy chain, Fab light chain | 著者 | Jiang, X. | 登録日 | 2013-11-12 | 公開日 | 2014-11-12 | 最終更新日 | 2015-04-22 | 実験手法 | X-RAY DIFFRACTION (2.41 Å) | 主引用文献 | Epitope characterization of an anti-PD-L1 antibody using orthogonal approaches. J.Mol.Recognit., 28, 2015
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4GV9
| Lassa nucleoprotein C-terminal domain in complex with triphosphated dsRNA soaking for 5 min | 分子名称: | MANGANESE (II) ION, Nucleoprotein, RNA (5'-R(*(GTP)P*GP*GP*C)-3'), ... | 著者 | Jiang, X, Huang, Q, Wang, W, Dong, H, Ly, H, Liang, Y, Dong, C. | 登録日 | 2012-08-30 | 公開日 | 2013-05-01 | 最終更新日 | 2024-02-28 | 実験手法 | X-RAY DIFFRACTION (2.46 Å) | 主引用文献 | Structures of Arenaviral Nucleoproteins with Triphosphate dsRNA Reveal a Unique Mechanism of Immune Suppression. J.Biol.Chem., 288, 2013
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4GVE
| Tacaribe nucleoprotein structure | 分子名称: | MAGNESIUM ION, Nucleoprotein, ZINC ION | 著者 | Jiang, X, Huang, Q, Wang, W, Dong, H, Ly, H, Liang, Y, Dong, C. | 登録日 | 2012-08-30 | 公開日 | 2013-05-01 | 最終更新日 | 2023-09-13 | 実験手法 | X-RAY DIFFRACTION (1.73 Å) | 主引用文献 | Structures of Arenaviral Nucleoproteins with Triphosphate dsRNA Reveal a Unique Mechanism of Immune Suppression. J.Biol.Chem., 288, 2013
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4GV6
| Structures of Lassa and Tacaribe viral nucleoproteins with or without 5 triphosphate dsRNA substrate reveal a unique 3 -5 exoribonuclease mechanism to suppress type I interferon production | 分子名称: | MANGANESE (II) ION, Nucleoprotein, RNA (5'-R(*(GTP)P*GP*GP*C)-3'), ... | 著者 | Jiang, X, Huang, Q, Wang, W, Dong, H, Ly, H, Liang, Y, Dong, C. | 登録日 | 2012-08-30 | 公開日 | 2013-05-01 | 最終更新日 | 2024-02-28 | 実験手法 | X-RAY DIFFRACTION (1.98 Å) | 主引用文献 | Structures of Arenaviral Nucleoproteins with Triphosphate dsRNA Reveal a Unique Mechanism of Immune Suppression. J.Biol.Chem., 288, 2013
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4GV3
| Structures of Lassa and Tacaribe viral nucleoproteins with or without 5 triphosphate dsRNA substrate reveal a unique 3 -5 exoribonuclease mechanism to suppress type I interferon production | 分子名称: | MANGANESE (II) ION, Nucleoprotein, RNA (5'-R(*(GTP)P*GP*GP*C)-3'), ... | 著者 | Jiang, X, Huang, Q, Wang, W, Dong, H, Ly, H, Liang, Y, Dong, C. | 登録日 | 2012-08-30 | 公開日 | 2013-05-01 | 最終更新日 | 2024-02-28 | 実験手法 | X-RAY DIFFRACTION (1.68 Å) | 主引用文献 | Structures of Arenaviral Nucleoproteins with Triphosphate dsRNA Reveal a Unique Mechanism of Immune Suppression. J.Biol.Chem., 288, 2013
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4JAJ
| Crystal Structure of Aurora Kinase A in complex with BENZO[C][1,8]NAPHTHYRIDIN-6(5H)-ONE | 分子名称: | Aurora kinase A, benzo[c][1,8]naphthyridin-6(5H)-one | 著者 | Jiang, X, Josephson, K, Huck, B, Goutopoulos, A, Karra, S. | 登録日 | 2013-02-18 | 公開日 | 2013-05-22 | 最終更新日 | 2023-09-20 | 実験手法 | X-RAY DIFFRACTION (2.7 Å) | 主引用文献 | SAR and evaluation of novel 5H-benzo[c][1,8]naphthyridin-6-one analogs as Aurora kinase inhibitors. Bioorg.Med.Chem.Lett., 23, 2013
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4JAI
| Crystal Structure of Aurora Kinase A in complex with N-{4-[(6-oxo-5,6-dihydrobenzo[c][1,8]naphthyridin-1-yl)amino]phenyl}benzamide | 分子名称: | Aurora kinase A, N-{4-[(6-oxo-5,6-dihydrobenzo[c][1,8]naphthyridin-1-yl)amino]phenyl}benzamide | 著者 | Jiang, X, Josephson, K, Huck, B, Goutopoulos, A, Karra, S. | 登録日 | 2013-02-18 | 公開日 | 2013-05-22 | 最終更新日 | 2023-09-20 | 実験手法 | X-RAY DIFFRACTION (3.2 Å) | 主引用文献 | SAR and evaluation of novel 5H-benzo[c][1,8]naphthyridin-6-one analogs as Aurora kinase inhibitors. Bioorg.Med.Chem.Lett., 23, 2013
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6JMN
| Crystal structure of Ostrinia furnacalis Chitinase h complexed with compound 2-8-s2 | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 6-azanyl-11-methyl-2-oxidanylidene-7-[[(2R)-oxolan-2-yl]methyl]-N-(pyridin-3-ylmethyl)-1,9-diaza-7-azoniatricyclo[8.4.0.0^{3,8}]tetradeca-3(8),4,6,9,11,13-hexaene-5-carboxamide, Chitinase | 著者 | Jiang, X, Yang, Q. | 登録日 | 2019-03-12 | 公開日 | 2020-05-06 | 最終更新日 | 2024-10-16 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | A Series of Compounds Bearing a Dipyrido-Pyrimidine Scaffold Acting as Novel Human and Insect Pest Chitinase Inhibitors. J.Med.Chem., 63, 2020
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6JK9
| Crystal structure of Serratia marcescens Chitinase B complexed with compound 2-8-14 | 分子名称: | 6-azanyl-2-oxidanylidene-N-[(1S)-1-phenylethyl]-7-(phenylmethyl)-1$l^{4},9-diaza-7-azoniatricyclo[8.4.0.0^{3,8}]tetradeca-1(14),3(8),4,6,10,12-hexaene-5-carboxamide, Chitinase | 著者 | Jiang, X, Yang, Q. | 登録日 | 2019-02-27 | 公開日 | 2020-02-19 | 最終更新日 | 2024-10-09 | 実験手法 | X-RAY DIFFRACTION (2.312 Å) | 主引用文献 | A Series of Compounds Bearing a Dipyrido-Pyrimidine Scaffold Acting as Novel Human and Insect Pest Chitinase Inhibitors. J.Med.Chem., 63, 2020
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6JJR
| Crystal structure of human chitotriosidase-1 (hChit1) catalytic domain in complex with compound 2-8-14 | 分子名称: | 6-azanyl-2-oxidanylidene-N-[(1S)-1-phenylethyl]-7-(phenylmethyl)-1$l^{4},9-diaza-7-azoniatricyclo[8.4.0.0^{3,8}]tetradeca-1(14),3(8),4,6,10,12-hexaene-5-carboxamide, Chitotriosidase-1 | 著者 | Jiang, X, Yang, Q. | 登録日 | 2019-02-26 | 公開日 | 2020-02-19 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (1.834 Å) | 主引用文献 | A Series of Compounds Bearing a Dipyrido-Pyrimidine Scaffold Acting as Novel Human and Insect Pest Chitinase Inhibitors. J.Med.Chem., 63, 2020
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6JVB
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6JV9
| Crystal Structure of Human CRMP2 1-532, unmodified | 分子名称: | 1,2-ETHANEDIOL, 2,3-DIHYDROXY-1,4-DITHIOBUTANE, Dihydropyrimidinase-related protein 2, ... | 著者 | Jiang, X, Ogawa, T, Hirokawa, N. | 登録日 | 2019-04-16 | 公開日 | 2019-10-09 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (2.26 Å) | 主引用文献 | Enhanced carbonyl stress induces irreversible multimerization of CRMP2 in schizophrenia pathogenesis. Life Sci Alliance, 2, 2019
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6JK6
| Crystal structure of human chitotriosidase-1 (hCHIT) catalytic domain in complex with compound 2-8-s2 | 分子名称: | 6-azanyl-11-methyl-2-oxidanylidene-7-[[(2R)-oxolan-2-yl]methyl]-N-(pyridin-3-ylmethyl)-1,9-diaza-7-azoniatricyclo[8.4.0.0^{3,8}]tetradeca-3(8),4,6,9,11,13-hexaene-5-carboxamide, Chitotriosidase-1 | 著者 | Jiang, X, Yang, Q. | 登録日 | 2019-02-27 | 公開日 | 2020-02-19 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (1.571 Å) | 主引用文献 | A Series of Compounds Bearing a Dipyrido-Pyrimidine Scaffold Acting as Novel Human and Insect Pest Chitinase Inhibitors. J.Med.Chem., 63, 2020
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7CLA
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7C92
| Structure of Serratia marcescens chitinase B complexed with compound 6k | 分子名称: | 6-azanyl-11-methyl-2-oxidanylidene-N-(pyridin-3-ylmethyl)-1,7,9-triazatricyclo[8.4.0.0^3,8]tetradeca-3(8),4,6,9,11,13-hexaene-5-carboxamide, Chitinase | 著者 | Jiang, X, Yuan, P.T. | 登録日 | 2020-06-04 | 公開日 | 2021-06-09 | 最終更新日 | 2024-10-09 | 実験手法 | X-RAY DIFFRACTION (2.32 Å) | 主引用文献 | Discovery of novel Chitinase Inhibitors with a scaffold of dipyridopyrimidine-3-carboxamide via Structure-based Rational Design To Be Published
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7CB1
| Structure of Serratia marcescens chitinase B complexed with compound 6q | 分子名称: | 6-azanyl-11-methyl-2-oxidanylidene-N-[(1S)-1-pyridin-3-ylethyl]-1,7,9-triazatricyclo[8.4.0.0^{3,8}]tetradeca-3,5,7,9,11,13-hexaene-5-carboxamide, Chitinase B | 著者 | Jiang, X, Yuan, P.T. | 登録日 | 2020-06-10 | 公開日 | 2021-06-16 | 最終更新日 | 2024-10-23 | 実験手法 | X-RAY DIFFRACTION (1.98 Å) | 主引用文献 | Discovery of novel Chitinase Inhibitors with a scaffold of dipyridopyrimidine-3-carboxamide via Structure-based Rational Design To Be Published
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