3COC
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3COD
| Crystal Structure of T90A/D115A mutant of Bacteriorhodopsin | 分子名称: | Bacteriorhodopsin, RETINAL | 著者 | Joh, N.H, Min, A, Faham, S, Bowie, J.U. | 登録日 | 2008-03-27 | 公開日 | 2008-04-08 | 最終更新日 | 2024-10-30 | 実験手法 | X-RAY DIFFRACTION (2.7 Å) | 主引用文献 | Modest stabilization by most hydrogen-bonded side-chain interactions in membrane proteins. Nature, 453, 2008
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4P6L
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4P6J
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4P6K
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3HAR
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3HAP
| Crystal structure of bacteriorhodopsin mutant L111A crystallized from bicelles | 分子名称: | 3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]-1-PROPANESULFONATE, Bacteriorhodopsin, DECANE, ... | 著者 | Joh, N.H, Yang, D, Bowie, J.U. | 登録日 | 2009-05-02 | 公開日 | 2009-09-22 | 最終更新日 | 2024-10-30 | 実験手法 | X-RAY DIFFRACTION (1.6 Å) | 主引用文献 | Similar energetic contributions of packing in the core of membrane and water-soluble proteins. J.Am.Chem.Soc., 131, 2009
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3HAS
| Crystal structure of bacteriorhodopsin mutant L152A crystallized from bicelles | 分子名称: | 3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]-1-PROPANESULFONATE, Bacteriorhodopsin, DECANE, ... | 著者 | Joh, N.H, Yang, D, Bowie, J.U. | 登録日 | 2009-05-02 | 公開日 | 2009-09-22 | 最終更新日 | 2021-10-13 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | Similar energetic contributions of packing in the core of membrane and water-soluble proteins. J.Am.Chem.Soc., 131, 2009
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3HAQ
| Crystal structure of bacteriorhodopsin mutant I148A crystallized from bicelles | 分子名称: | 3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]-1-PROPANESULFONATE, Bacteriorhodopsin, DECANE, ... | 著者 | Joh, N.H, Yang, D, Bowie, J.U. | 登録日 | 2009-05-02 | 公開日 | 2009-09-22 | 最終更新日 | 2024-10-30 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Similar energetic contributions of packing in the core of membrane and water-soluble proteins. J.Am.Chem.Soc., 131, 2009
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3HAN
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3HAO
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7M8J
| SARS-CoV-2 S-NTD + Fab CM25 | 分子名称: | CM25 Fab - Heavy Chain, CM25 Fab - Light Chain, Spike protein S1 | 著者 | Johnson, N.V, Mclellan, J.S. | 登録日 | 2021-03-29 | 公開日 | 2021-05-19 | 最終更新日 | 2021-06-16 | 実験手法 | ELECTRON MICROSCOPY (3.48 Å) | 主引用文献 | Prevalent, protective, and convergent IgG recognition of SARS-CoV-2 non-RBD spike epitopes. Science, 372, 2021
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8V5A
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8V5K
| Structure of the Human Respirovirus 3 Fusion Protein Bound to Camelid Nanobodies 4C03 and 4C06 | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, Camelid Nanobody 4C03, Camelid Nanobody 4C06, ... | 著者 | Johnson, N.V, Ramamohan, A.R, McLellan, J.S. | 登録日 | 2023-11-30 | 公開日 | 2024-05-22 | 最終更新日 | 2024-10-30 | 実験手法 | ELECTRON MICROSCOPY (2.6 Å) | 主引用文献 | Structural basis for potent neutralization of human respirovirus type 3 by protective single-domain camelid antibodies. Nat Commun, 15, 2024
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8V62
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8VCR
| SARS-CoV-2 Spike S2 bound to Fab 54043-5 | 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, 54043-5 Fab Heavy Chain, ... | 著者 | Johnson, N.V, McLellan, J.S. | 登録日 | 2023-12-14 | 公開日 | 2024-07-31 | 最終更新日 | 2024-10-23 | 実験手法 | ELECTRON MICROSCOPY (3 Å) | 主引用文献 | Discovery and characterization of a pan-betacoronavirus S2-binding antibody. Structure, 2024
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7T01
| SARS-CoV-2 S-RBD + Fab 54042-4 | 分子名称: | 54042-4 Fab - Heavy Chain, 54042-4 Fab - Light Chain, Spike protein S1 | 著者 | Johnson, N.V, Mclellan, J.S. | 登録日 | 2021-11-29 | 公開日 | 2022-04-13 | 実験手法 | ELECTRON MICROSCOPY (2.69 Å) | 主引用文献 | Potent neutralization of SARS-CoV-2 variants of concern by an antibody with an uncommon genetic signature and structural mode of spike recognition. Cell Rep, 37, 2021
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2MUZ
| ssNMR structure of a designed rocker protein | 分子名称: | designed rocker protein | 著者 | Wang, T, Joh, N, Wu, Y, DeGrado, W.F, Hong, M. | 登録日 | 2014-09-18 | 公開日 | 2014-12-24 | 最終更新日 | 2015-01-14 | 実験手法 | SOLUTION NMR | 主引用文献 | De novo design of a transmembrane Zn2+-transporting four-helix bundle. Science, 346, 2014
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5J7D
| Computationally Designed Thioredoxin dF106 | 分子名称: | COPPER (II) ION, Designed Thioredoxin dF106 | 著者 | Horowitz, S, Johansen, N, Olsen, J.G, Winther, J.R. | 登録日 | 2016-04-06 | 公開日 | 2016-10-05 | 最終更新日 | 2024-01-10 | 実験手法 | X-RAY DIFFRACTION (2.4 Å) | 主引用文献 | Computational Redesign of Thioredoxin Is Hypersensitive toward Minor Conformational Changes in the Backbone Template. J.Mol.Biol., 428, 2016
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1VYQ
| Novel inhibitors of Plasmodium Falciparum dUTPase provide a platform for anti-malarial drug design | 分子名称: | 2,3-DEOXY-3-FLUORO-5-O-TRITYLURIDINE, DEOXYURIDINE 5'-TRIPHOSPHATE NUCLEOTIDOHYDROLASE | 著者 | Whittingham, J.L, Leal, I, Kasinathan, G, Nguyen, C, Bell, E, Jones, A.F, Berry, C, Benito, A, Turkenburg, J.P, Dodson, E.J, Ruiz Perez, L.M, Wilkinson, A.J, Johansson, N.G, Brun, R, Gilbert, I.H, Gonzalez Pacanowska, D, Wilson, K.S. | 登録日 | 2004-05-05 | 公開日 | 2005-05-26 | 最終更新日 | 2023-12-13 | 実験手法 | X-RAY DIFFRACTION (2.4 Å) | 主引用文献 | Dutpase as a Platform for Antimalarial Drug Design: Structural Basis for the Selectivity of a Class of Nucleoside Inhibitors. Structure, 13, 2005
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1RCM
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1EET
| HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH THE INHIBITOR MSC204 | 分子名称: | 1-(5-BROMO-PYRIDIN-2-YL)-3-[2-(6-FLUORO-2-HYDROXY-3-PROPIONYL-PHENYL)-CYCLOPROPYL]-UREA, HIV-1 REVERSE TRANSCRIPTASE | 著者 | Hogberg, M, Sahlberg, C, Engelhardt, P, Noreen, R, Kangasmetsa, J, Johansson, N.G, Oberg, B, Vrang, L, Zhang, H, Sahlberg, B.L, Unge, T, Lovgren, S, Fridborg, K, Backbro, K. | 登録日 | 2000-02-03 | 公開日 | 2001-02-07 | 最終更新日 | 2024-02-07 | 実験手法 | X-RAY DIFFRACTION (2.73 Å) | 主引用文献 | Urea-PETT compounds as a new class of HIV-1 reverse transcriptase inhibitors. 3. Synthesis and further structure-activity relationship studies of PETT analogues. J.Med.Chem., 42, 1999
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2Y8C
| Plasmodium falciparum dUTPase in complex with a trityl ligand | 分子名称: | (2S)-2-[(2,4-dioxopyrimidin-1-yl)methyl]-N-(2-hydroxyethyl)-4-trityloxy-butanamide, DEOXYURIDINE 5'-TRIPHOSPHATE NUCLEOTIDOHYDROLASE, SULFATE ION | 著者 | Baragana, B, McCarthy, O, Sanchez, P, Bosch, C, Kaiser, M, Brun, R, Whittingham, J.L, Roberts, S, Zhou, X.-X, Wilson, K.S, Johansson, N.G, Gonzalez-Pacanowska, D, Gilbert, I.H. | 登録日 | 2011-02-04 | 公開日 | 2012-03-07 | 最終更新日 | 2023-12-20 | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | 主引用文献 | Beta-Branched Acyclic Nucleoside Analogues as Inhibitors of Plasmodium Falciparum Dutpase Bioorg.Med.Chem., 19, 2011
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5AR1
| Crystal structure of Cdc11 from Saccharomyces cerevisiae | 分子名称: | CELL DIVISION CONTROL PROTEIN 11 | 著者 | Brausemann, A, Gerhardt, S, Schott, A.K, Einsle, O, Grosse-Berkenbusch, A, Johnsson, N, Gronemeyer, T. | 登録日 | 2015-09-23 | 公開日 | 2016-01-27 | 最終更新日 | 2024-01-10 | 実験手法 | X-RAY DIFFRACTION (2.85 Å) | 主引用文献 | Crystal Structure of Cdc11, a Septin Subunit from Saccharomyces Cerevisiae. J.Struct.Biol., 193, 2016
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3T60
| 5'-Diphenyl Nucleoside Inhibitors of Plasmodium falciparum dUTPase | 分子名称: | 2',5'-dideoxy-5'-(tritylamino)uridine, Deoxyuridine 5'-triphosphate nucleotidohydrolase, putative, ... | 著者 | Hampton, S.E, Baragana, B, Schipani, A, Bosch-Navarrete, C, Musso-Buendia, A, Recio, E, Kaiser, M, Whittingham, J.L, Roberts, S.M, Shevtsov, M, Brannigan, J.A, Kahnberg, P, Brun, R, Wilson, K.S, Gonzalez-Pacanowska, D, Johansson, N.G, Gilbert, I.H. | 登録日 | 2011-07-28 | 公開日 | 2012-08-29 | 最終更新日 | 2023-09-13 | 実験手法 | X-RAY DIFFRACTION (2.396 Å) | 主引用文献 | Design, synthesis, and evaluation of 5'-diphenyl nucleoside analogues as inhibitors of the Plasmodium falciparum dUTPase. Chemmedchem, 6, 2011
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