1OP9
| Complex of human lysozyme with camelid VHH HL6 antibody fragment | 分子名称: | HL6 camel VHH fragment, Lysozyme C | 著者 | Dumoulin, M, Last, A.M, Desmyter, A, Decanniere, K, Canet, D, Larsson, G, Spencer, A, Archer, D.B, Sasse, J, Muyldermans, S, Wyns, L, Redfield, C, Matagne, A, Robinson, C.V, Dobson, C.M. | 登録日 | 2003-03-05 | 公開日 | 2003-10-14 | 最終更新日 | 2023-08-16 | 実験手法 | X-RAY DIFFRACTION (1.86 Å) | 主引用文献 | A camelid antibody fragment inhibits the formation of amyloid fibrils by human lysozyme Nature, 424, 2003
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4PIR
| X-ray structure of the mouse serotonin 5-HT3 receptor | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 5-hydroxytryptamine receptor 3A, ... | 著者 | Hassaine, G, Deluz, C, Grasso, L, Wyss, R, Tol, M.B, Hovius, R, Graff, A, Stahlberg, H, Tomizaki, T, Desmyter, A, Moreau, C, Li, X.-D, Poitevin, F, Vogel, H, Nury, H. | 登録日 | 2014-05-09 | 公開日 | 2014-08-06 | 最終更新日 | 2023-12-27 | 実験手法 | X-RAY DIFFRACTION (3.5 Å) | 主引用文献 | X-ray structure of the mouse serotonin 5-HT3 receptor. Nature, 512, 2014
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4QGY
| Camelid (llama) nanobody n25 (VHH) against type 6 secretion system TssM protein | 分子名称: | nanobody n25, VH domain | 著者 | Nguyen, V.S, Desmyter, A, Le, T.T.H, Durand, E, Kellenberger, C, Douzi, B, Spinelli, S, Cascales, E, Cambillau, C, Roussel, A. | 登録日 | 2014-05-26 | 公開日 | 2015-04-08 | 最終更新日 | 2023-11-08 | 実験手法 | X-RAY DIFFRACTION (1.38 Å) | 主引用文献 | Inhibition of Type VI Secretion by an Anti-TssM Llama Nanobody. Plos One, 10, 2015
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4QLR
| Llama nanobody n02 raised against EAEC T6SS TssM | 分子名称: | Llama nanobody n02 VH domain | 著者 | Nguyen, V.S, Desmyter, A, Le, T.T.H, Durand, E, Kellenberger, C, Douzi, B, Spinelli, S, Cascales, E, Cambillau, C, Roussel, A. | 登録日 | 2014-06-13 | 公開日 | 2015-04-08 | 最終更新日 | 2023-11-08 | 実験手法 | X-RAY DIFFRACTION (1.7 Å) | 主引用文献 | Inhibition of Type VI Secretion by an Anti-TssM Llama Nanobody. Plos One, 10, 2015
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5M30
| Structure of TssK from T6SS EAEC in complex with nanobody nb18 | 分子名称: | Anti-vesicular stomatitis virus N VHH, Type VI secretion protein | 著者 | Nguyen, V.S, Cambillau, C, Spinelli, C, Desmyter, A, Legrand, P, Cascales, E. | 登録日 | 2016-10-13 | 公開日 | 2017-06-21 | 最終更新日 | 2017-09-06 | 実験手法 | X-RAY DIFFRACTION (2.6 Å) | 主引用文献 | Type VI secretion TssK baseplate protein exhibits structural similarity with phage receptor-binding proteins and evolved to bind the membrane complex. Nat Microbiol, 2, 2017
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5M2W
| Structure of nanobody nb18 raised against TssK from E. coli T6SS | 分子名称: | Llama nanobody nb8 against TssK from T6SS, SULFATE ION | 著者 | Cambillau, C, Nguyen, V.S, Spinelli, S, Desmyter, A. | 登録日 | 2016-10-13 | 公開日 | 2017-06-28 | 最終更新日 | 2017-08-30 | 実験手法 | X-RAY DIFFRACTION (1.5 Å) | 主引用文献 | Type VI secretion TssK baseplate protein exhibits structural similarity with phage receptor-binding proteins and evolved to bind the membrane complex. Nat Microbiol, 2, 2017
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5M2Y
| Structure of TssK C-terminal domain from E. coli T6SS | 分子名称: | TssK C | 著者 | Cambillau, C, Nguyen, V.S, Spinelli, S, Desmyter, A, Legrand, P. | 登録日 | 2016-10-13 | 公開日 | 2017-06-28 | 最終更新日 | 2024-01-17 | 実験手法 | X-RAY DIFFRACTION (1.61 Å) | 主引用文献 | Type VI secretion TssK baseplate protein exhibits structural similarity with phage receptor-binding proteins and evolved to bind the membrane complex. Nat Microbiol, 2, 2017
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1LJL
| Wild Type pI258 S. aureus arsenate reductase | 分子名称: | POTASSIUM ION, arsenate reductase | 著者 | Messens, J, Martins, J.C, Van Belle, K, Brosens, E, Desmyter, A, De Gieter, M, Wieruszeski, J.M, Willem, R, Wyns, L, Zegers, I. | 登録日 | 2002-04-21 | 公開日 | 2002-08-07 | 最終更新日 | 2023-08-16 | 実験手法 | X-RAY DIFFRACTION (2.01 Å) | 主引用文献 | All intermediates of the arsenate reductase mechanism, including an intramolecular dynamic disulfide cascade. Proc.Natl.Acad.Sci.USA, 99, 2002
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1LK0
| Disulfide intermediate of C89L Arsenate reductase from pI258 | 分子名称: | CHLORIDE ION, POTASSIUM ION, arsenate reductase | 著者 | Messens, J, Martins, J.C, Van Belle, K, Brosens, E, Desmyter, A, De Gieter, M, Wieruszeski, J.M, Willem, R, Wyns, L, Zegers, I. | 登録日 | 2002-04-23 | 公開日 | 2002-08-07 | 最終更新日 | 2023-08-16 | 実験手法 | X-RAY DIFFRACTION (1.6 Å) | 主引用文献 | All intermediates of the arsenate reductase mechanism, including an intramolecular dynamic disulfide cascade. Proc.Natl.Acad.Sci.USA, 99, 2002
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5M2J
| Complex between human TNF alpha and Llama VHH2 | 分子名称: | Anti-(ED-B) scFV, Tumor necrosis factor | 著者 | Cambillau, C, Spinelli, S, Desmyter, A, de Haard, H. | 登録日 | 2016-10-13 | 公開日 | 2017-08-30 | 最終更新日 | 2024-01-17 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | Bivalent Llama Single-Domain Antibody Fragments against Tumor Necrosis Factor Have Picomolar Potencies due to Intramolecular Interactions. Front Immunol, 8, 2017
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5M2I
| Structure of human Tumor Necrosis Factor (TNF) in complex with the Llama VHH1 | 分子名称: | Tumor necrosis factor, VHH1 | 著者 | Cambillau, C, Spinelli, S, Desmyter, A, de Haard, H. | 登録日 | 2016-10-13 | 公開日 | 2017-08-30 | 最終更新日 | 2024-01-17 | 実験手法 | X-RAY DIFFRACTION (2.15 Å) | 主引用文献 | Bivalent Llama Single-Domain Antibody Fragments against Tumor Necrosis Factor Have Picomolar Potencies due to Intramolecular Interactions. Front Immunol, 8, 2017
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5M2M
| Complex between human TNF alpha and Llama VHH3 | 分子名称: | Llama nanobody VHH3, Tumor necrosis factor | 著者 | Cambillau, C, Spinelli, S, Desmyter, A, de Haard, H. | 登録日 | 2016-10-13 | 公開日 | 2017-08-30 | 最終更新日 | 2024-01-17 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Bivalent Llama Single-Domain Antibody Fragments against Tumor Necrosis Factor Have Picomolar Potencies due to Intramolecular Interactions. Front Immunol, 8, 2017
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6GZP
| Llama nanobody PorM_02 structure determined at room temperature by in-situ diffraction in ChipX microfluidic device | 分子名称: | Nanobody | 著者 | Roche, J, Gaubert, A, Desmyter, A, De Wijn, R, Sauter, C, Roussel, A. | 登録日 | 2018-07-04 | 公開日 | 2018-07-18 | 最終更新日 | 2024-01-17 | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | 主引用文献 | A simple and versatile microfluidic device for efficient biomacromolecule crystallization and structural analysis by serial crystallography. Iucrj, 6, 2019
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