8JY0
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![BU of 8jy0 by Molmil](/molmil-images/mine/8jy0) | Crystal structure of RhoBAST complexed with TMR-DN | 分子名称: | 2,4-dinitroaniline, 5-aminocarbonyl-2-[3-(dimethylamino)-6-dimethylazaniumylidene-xanthen-9-yl]benzoate, GUANOSINE-5'-DIPHOSPHATE, ... | 著者 | Zhang, Y, Xiao, Y, Xu, Z, Fang, X. | 登録日 | 2023-07-02 | 公開日 | 2024-05-29 | 実験手法 | X-RAY DIFFRACTION (2.75 Å) | 主引用文献 | Structural mechanisms for binding and activation of a contact-quenched fluorophore by RhoBAST. Nat Commun, 15, 2024
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6JFI
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![BU of 6jfi by Molmil](/molmil-images/mine/6jfi) | The symmetric-reconstructed cryo-EM structure of Zika virus-FabZK2B10 complex | 分子名称: | FabZK2B10 heavy chain, FabZK2B10 light chain, ZIKV structural protein E, ... | 著者 | Wang, L, Wang, R.K, Wang, L, Ben, H.J, Yu, L, Gao, F, Shi, X.L, Yin, C.B, Zhang, F.C, Xiang, Y, Zhang, L.Q. | 登録日 | 2019-02-08 | 公開日 | 2019-04-10 | 最終更新日 | 2024-03-27 | 実験手法 | ELECTRON MICROSCOPY (11 Å) | 主引用文献 | Structural Basis for Neutralization and Protection by a Zika Virus-Specific Human Antibody. Cell Rep, 26, 2019
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6QX7
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6QYM
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6QZF
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![BU of 6qzf by Molmil](/molmil-images/mine/6qzf) | The cryo-EM structure of the collar complex and tail axis in genome emptied bacteriophage phi29 | 分子名称: | Portal protein, Pre-neck appendage protein, Proximal tail tube connector protein | 著者 | Xu, J, Wang, D, Gui, M, Xiang, Y. | 登録日 | 2019-03-11 | 公開日 | 2019-06-12 | 最終更新日 | 2024-05-15 | 実験手法 | ELECTRON MICROSCOPY (3.8 Å) | 主引用文献 | Structural assembly of the tailed bacteriophage φ29. Nat Commun, 10, 2019
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6QZ9
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![BU of 6qz9 by Molmil](/molmil-images/mine/6qz9) | The cryo-EM structure of the collar complex and tail axis in bacteriophage phi29 | 分子名称: | Portal protein, Pre-neck appendage protein, Proximal tail tube connector protein | 著者 | Xu, J, Wang, D, Gui, M, Xiang, Y. | 登録日 | 2019-03-11 | 公開日 | 2019-06-12 | 最終更新日 | 2024-05-15 | 実験手法 | ELECTRON MICROSCOPY (3.3 Å) | 主引用文献 | Structural assembly of the tailed bacteriophage φ29. Nat Commun, 10, 2019
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6QYD
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![BU of 6qyd by Molmil](/molmil-images/mine/6qyd) | Cryo-EM structure of the head in mature bacteriophage phi29 | 分子名称: | Capsid fiber protein, Major capsid protein | 著者 | Xu, J.W, Wang, D.H, Gui, M, Xiang, Y. | 登録日 | 2019-03-08 | 公開日 | 2019-06-12 | 最終更新日 | 2024-05-15 | 実験手法 | ELECTRON MICROSCOPY (3.2 Å) | 主引用文献 | Structural assembly of the tailed bacteriophage φ29. Nat Commun, 10, 2019
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6QZ0
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![BU of 6qz0 by Molmil](/molmil-images/mine/6qz0) | The cryo-EM structure of the head of the genome empited bacteriophage phi29 | 分子名称: | Capsid fiber protein, Major capsid protein | 著者 | Xu, J, Wang, D, Gui, M, Xiang, Y. | 登録日 | 2019-03-10 | 公開日 | 2019-06-12 | 最終更新日 | 2024-05-15 | 実験手法 | ELECTRON MICROSCOPY (3.2 Å) | 主引用文献 | Structural assembly of the tailed bacteriophage φ29. Nat Commun, 10, 2019
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1KV0
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![BU of 1kv0 by Molmil](/molmil-images/mine/1kv0) | Cis/trans Isomerization of Non-prolyl Peptide Bond Observed in Crystal Structure of an Scorpion Toxin | 分子名称: | Alpha-like toxin BmK-M7 | 著者 | Guan, R.J, He, X.L, Wang, M, Xiang, Y, Wang, D.C. | 登録日 | 2002-01-23 | 公開日 | 2003-09-16 | 最終更新日 | 2023-10-25 | 実験手法 | X-RAY DIFFRACTION (1.4 Å) | 主引用文献 | Structural mechanism governing cis and trans isomeric states and an intramolecular switch for cis/trans isomerization of a non-proline peptide bond observed in crystal structures of scorpion toxins. J.Mol.Biol., 341, 2004
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6QYJ
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6QYY
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![BU of 6qyy by Molmil](/molmil-images/mine/6qyy) | The crystal structure of head fiber gp8.5 N base in bacteriophage phi29 | 分子名称: | Capsid fiber protein, SULFATE ION | 著者 | Xu, J, Wang, D, Gui, M, Xiang, Y. | 登録日 | 2019-03-10 | 公開日 | 2019-06-12 | 最終更新日 | 2024-05-15 | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | 主引用文献 | Structural assembly of the tailed bacteriophage φ29. Nat Commun, 10, 2019
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6QVK
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6QYZ
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2WZS
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![BU of 2wzs by Molmil](/molmil-images/mine/2wzs) | Structure of the Family GH92 Inverting Mannosidase BT3990 from Bacteroides thetaiotaomicron VPI-5482 in complex with Mannoimidazole | 分子名称: | (5R,6R,7S,8R)-5-(HYDROXYMETHYL)-5,6,7,8-TETRAHYDROIMIDAZO[1,2-A]PYRIDINE-6,7,8-TRIOL, CALCIUM ION, GLYCEROL, ... | 著者 | Zhu, Y, Suits, M.D.L, Thompson, A, Chavan, S, Dinev, Z, Dumon, C, Smith, N, Moremen, K.W, Xiang, Y, Siriwardena, A, Williams, S.J, Gilbert, H.J, Davies, G.J. | 登録日 | 2009-12-02 | 公開日 | 2009-12-29 | 最終更新日 | 2024-05-01 | 実験手法 | X-RAY DIFFRACTION (2.25 Å) | 主引用文献 | Mechanistic Insights Into a Ca2+-Dependent Family of A-Mannosidases in a Human Gut Symbiont. Nat.Chem.Biol., 6, 2010
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4U03
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4U0M
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5CYW
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![BU of 5cyw by Molmil](/molmil-images/mine/5cyw) | Crystal Structure of Vaccinia Virus C7 | 分子名称: | GLYCEROL, Interferon antagonist C7 | 著者 | Krumm, B.E, Meng, X, Li, Y, Xiang, Y, Deng, J. | 登録日 | 2015-07-30 | 公開日 | 2015-11-18 | 最終更新日 | 2024-03-06 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Structural basis for antagonizing a host restriction factor by C7 family of poxvirus host-range proteins. Proc.Natl.Acad.Sci.USA, 112, 2015
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5CZ3
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![BU of 5cz3 by Molmil](/molmil-images/mine/5cz3) | Crystal Structure of Myxoma Virus M64 | 分子名称: | BETA-MERCAPTOETHANOL, M64R | 著者 | Krumm, B.E, Meng, X, Li, Y, Xiang, Y, Deng, J. | 登録日 | 2015-07-31 | 公開日 | 2015-11-18 | 最終更新日 | 2023-09-27 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Structural basis for antagonizing a host restriction factor by C7 family of poxvirus host-range proteins. Proc.Natl.Acad.Sci.USA, 112, 2015
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1U6T
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![BU of 1u6t by Molmil](/molmil-images/mine/1u6t) | Crystal structure of the human SH3 binding glutamic-rich protein like | 分子名称: | CITRIC ACID, SH3 domain-binding glutamic acid-rich-like protein | 著者 | Yin, L, Xiang, Y, Yang, N, Zhu, D.-Y, Huang, R.-H, Wang, D.-C. | 登録日 | 2004-08-01 | 公開日 | 2005-08-09 | 最終更新日 | 2024-03-13 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | Crystal structure of human SH3BGRL protein: the first structure of the human SH3BGR family representing a novel class of thioredoxin fold proteins Proteins, 61, 2005
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6N13
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![BU of 6n13 by Molmil](/molmil-images/mine/6n13) | UbcH7-Ub Complex with R0RBR Parkin and phosphoubiquitin | 分子名称: | E3 ubiquitin-protein ligase parkin, Ubiquitin-conjugating enzyme E2 L3, ZINC ION, ... | 著者 | Condos, T.E.C, Dunkerley, K.M, Freeman, E.A, Barber, K.R, Aguirre, J.D, Chaugule, V.K, Xiao, Y, Konermann, L, Walden, H, Shaw, G.S. | 登録日 | 2018-11-08 | 公開日 | 2018-11-28 | 最終更新日 | 2020-01-08 | 実験手法 | SOLUTION NMR | 主引用文献 | Synergistic recruitment of UbcH7~Ub and phosphorylated Ubl domain triggers parkin activation. EMBO J., 37, 2018
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4N9B
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![BU of 4n9b by Molmil](/molmil-images/mine/4n9b) | Fragment-based Design of 3-Aminopyridine-derived Amides as Potent Inhibitors of Human Nicotinamide Phosphoribosyltransferase (NAMPT) | 分子名称: | 1-methyl-N-(pyridin-3-yl)-1H-pyrazole-5-carboxamide, Nicotinamide phosphoribosyltransferase, PHOSPHATE ION | 著者 | Dragovich, P.S, Zhao, G, Baumeister, T, Bravo, B, Giannetti, A.M, Ho, Y, Hua, R, Li, G, Liang, X, O'Brien, T, Skelton, N.J, Wang, C, Zhai, Q, Oh, A, Wang, W, Wang, Y, Xiao, Y, Yuen, P, Zak, M, Zheng, X. | 登録日 | 2013-10-20 | 公開日 | 2014-02-19 | 最終更新日 | 2023-09-20 | 実験手法 | X-RAY DIFFRACTION (2.859 Å) | 主引用文献 | Fragment-based design of 3-aminopyridine-derived amides as potent inhibitors of human nicotinamide phosphoribosyltransferase (NAMPT). Bioorg.Med.Chem.Lett., 24, 2014
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4N9E
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![BU of 4n9e by Molmil](/molmil-images/mine/4n9e) | Fragment-based Design of 3-Aminopyridine-derived Amides as Potent Inhibitors of Human Nicotinamide Phosphoribosyltransferase (NAMPT) | 分子名称: | 1,2-ETHANEDIOL, 1-[(1-benzoylpiperidin-4-yl)methyl]-N-(pyridin-3-yl)-1H-benzimidazole-5-carboxamide, 2,3-DIHYDROXY-1,4-DITHIOBUTANE, ... | 著者 | Dragovich, P.S, Zhao, G, Baumeister, T, Bravo, B, Giannetti, A.M, Ho, Y, Hua, R, Li, G, Liang, X, O'Brien, T, Skelton, N.J, Wang, C, Zhao, Q, Oh, A, Wang, W, Wang, Y, Xiao, Y, Yuen, P, Zak, M, Zheng, X. | 登録日 | 2013-10-20 | 公開日 | 2014-02-19 | 最終更新日 | 2024-02-28 | 実験手法 | X-RAY DIFFRACTION (1.72 Å) | 主引用文献 | Fragment-based design of 3-aminopyridine-derived amides as potent inhibitors of human nicotinamide phosphoribosyltransferase (NAMPT). Bioorg.Med.Chem.Lett., 24, 2014
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4N9D
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![BU of 4n9d by Molmil](/molmil-images/mine/4n9d) | Fragment-based Design of 3-Aminopyridine-derived Amides as Potent Inhibitors of Human Nicotinamide Phosphoribosyltransferase (NAMPT) | 分子名称: | 1,2-ETHANEDIOL, 4-({[(4-tert-butylphenyl)sulfonyl]amino}methyl)-N-(pyridin-3-yl)benzamide, Nicotinamide phosphoribosyltransferase, ... | 著者 | Dragovich, P.S, Zhao, G, Baumeister, T, Bravo, B, Giannetti, A.M, Ho, Y, Hua, R, Li, G, Liang, X, O'Brien, T, Skelton, N.J, Wang, C, Zhao, Q, Oh, A, Wang, W, Wang, Y, Xiao, Y, Yuen, P, Zak, M, Zheng, X. | 登録日 | 2013-10-20 | 公開日 | 2014-02-19 | 最終更新日 | 2024-02-28 | 実験手法 | X-RAY DIFFRACTION (1.701 Å) | 主引用文献 | Fragment-based design of 3-aminopyridine-derived amides as potent inhibitors of human nicotinamide phosphoribosyltransferase (NAMPT). Bioorg.Med.Chem.Lett., 24, 2014
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7KSP
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![BU of 7ksp by Molmil](/molmil-images/mine/7ksp) | Crystal structure of hSAMD9_DBD with DNA | 分子名称: | DNA, Sterile alpha motif domain-containing protein 9 | 著者 | Peng, S, Pathak, P, Xiang, Y, Deng, J. | 登録日 | 2020-11-23 | 公開日 | 2022-01-05 | 最終更新日 | 2024-05-22 | 実験手法 | X-RAY DIFFRACTION (2.8 Å) | 主引用文献 | Structure and function of an effector domain in antiviral factors and tumor suppressors SAMD9 and SAMD9L. Proc.Natl.Acad.Sci.USA, 119, 2022
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4N9C
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![BU of 4n9c by Molmil](/molmil-images/mine/4n9c) | Fragment-based Design of 3-Aminopyridine-derived Amides as Potent Inhibitors of Human Nicotinamide Phosphoribosyltransferase (NAMPT) | 分子名称: | 5-nitro-1H-benzimidazole, Nicotinamide phosphoribosyltransferase, PHOSPHATE ION | 著者 | Dragovich, P.S, Zhao, G, Baumeister, T, Bravo, B, Giannetti, A.M, Ho, Y, Hua, R, Li, G, Liang, X, O'Brien, T, Skelton, N.J, Wang, C, Zhao, Q, Oh, A, Wang, W, Wang, Y, Xiao, Y, Yuen, P, Zak, M, Zheng, X. | 登録日 | 2013-10-20 | 公開日 | 2014-02-19 | 最終更新日 | 2024-02-28 | 実験手法 | X-RAY DIFFRACTION (1.751 Å) | 主引用文献 | Fragment-based design of 3-aminopyridine-derived amides as potent inhibitors of human nicotinamide phosphoribosyltransferase (NAMPT). Bioorg.Med.Chem.Lett., 24, 2014
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