8IZE
 
 | | Crystal structure of intracellular B30.2 domain of BTN3A1 in complex with 4-HMBPP | | 分子名称: | Butyrophilin subfamily 3 member A1, DI(HYDROXYETHYL)ETHER, [(E)-3-(hydroxymethyl)pent-2-enyl] phosphono hydrogen phosphate | | 著者 | Yang, Y.Y, Yi, S.M, Huang, J.W, Chen, C.C, Guo, R.T. | | 登録日 | 2023-04-07 | | 公開日 | 2023-09-13 | | 最終更新日 | 2023-10-18 | | 実験手法 | X-RAY DIFFRACTION (1.4 Å) | | 主引用文献 | Phosphoantigens glue butyrophilin 3A1 and 2A1 to activate V gamma 9V delta 2 T cells.
Nature, 621, 2023
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3VGY
 | | Structure of HIV-1 gp41 NHR/fusion inhibitor complex P321 | | 分子名称: | CP32M, Envelope glycoprotein gp160, SULFATE ION | | 著者 | Yao, X, Waltersperger, S, Wang, M.T, Cui, S. | | 登録日 | 2011-08-22 | | 公開日 | 2012-06-13 | | 最終更新日 | 2023-11-08 | | 実験手法 | X-RAY DIFFRACTION (2.034 Å) | | 主引用文献 | Structural basis of potent and broad HIV-1 fusion inhibitor CP32M
J.Biol.Chem., 287, 2012
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3VIE
 | | HIV-gp41 fusion inhibitor Sifuvirtide | | 分子名称: | Envelope glycoprotein gp160, Sifuvirtide | | 著者 | Yao, X, Waltersperger, S, Wang, M.T, Cui, S. | | 登録日 | 2011-09-29 | | 公開日 | 2012-01-18 | | 最終更新日 | 2023-11-08 | | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | | 主引用文献 | Broad antiviral activity and crystal structure of HIV-1 fusion inhibitor sifuvirtide
J.Biol.Chem., 287, 2012
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7CO7
 | | HtrA-type protease AlgWS227A with decapeptide | | 分子名称: | 3-CYCLOHEXYL-1-PROPYLSULFONIC ACID, AlgW protein, decapeptide SVRDELRWVF | | 著者 | Li, T, Song, Y.J, Bao, R. | | 登録日 | 2020-08-04 | | 公開日 | 2021-03-10 | | 最終更新日 | 2023-11-29 | | 実験手法 | X-RAY DIFFRACTION (2.6 Å) | | 主引用文献 | Molecular Basis of the Versatile Regulatory Mechanism of HtrA-Type Protease AlgW from Pseudomonas aeruginosa.
Mbio, 12, 2021
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7CO5
 | | HtrA-type protease AlgW with decapeptide | | 分子名称: | AlgW protein, IMIDAZOLE, decapeptide SVRDELRWVF | | 著者 | Li, T, Song, Y.J, Bao, R. | | 登録日 | 2020-08-03 | | 公開日 | 2021-03-10 | | 最終更新日 | 2023-11-29 | | 実験手法 | X-RAY DIFFRACTION (2.345 Å) | | 主引用文献 | Molecular Basis of the Versatile Regulatory Mechanism of HtrA-Type Protease AlgW from Pseudomonas aeruginosa.
Mbio, 12, 2021
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7CO3
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7CO2
 | | HtrA-type protease AlgW with tripeptide | | 分子名称: | AlgW protein, IMIDAZOLE, TRP-VAL-PHE | | 著者 | Li, T, Song, Y.J, Bao, R. | | 登録日 | 2020-08-03 | | 公開日 | 2021-03-10 | | 最終更新日 | 2023-11-29 | | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | | 主引用文献 | Molecular Basis of the Versatile Regulatory Mechanism of HtrA-Type Protease AlgW from Pseudomonas aeruginosa.
Mbio, 12, 2021
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2ETM
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2EY4
 | | Crystal Structure of a Cbf5-Nop10-Gar1 Complex | | 分子名称: | Probable tRNA pseudouridine synthase B, Ribosome biogenesis protein Nop10, ZINC ION, ... | | 著者 | Rashid, R, Liang, B, Li, H, Southeast Collaboratory for Structural Genomics (SECSG) | | 登録日 | 2005-11-09 | | 公開日 | 2006-01-24 | | 最終更新日 | 2024-02-14 | | 実験手法 | X-RAY DIFFRACTION (2.11 Å) | | 主引用文献 | Crystal structure of a Cbf5-Nop10-Gar1 complex and implications in RNA-guided pseudouridylation and dyskeratosis congenita.
Mol.Cell, 21, 2006
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3VTP
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3VGX
 | | Structure of gp41 T21/Cp621-652 | | 分子名称: | ACETIC ACID, Envelope glycoprotein gp160, GLYCEROL | | 著者 | Yao, X, Waltersperger, S, Wang, M, Cui, S. | | 登録日 | 2011-08-22 | | 公開日 | 2012-04-25 | | 最終更新日 | 2023-11-08 | | 実験手法 | X-RAY DIFFRACTION (1.74 Å) | | 主引用文献 | Discovery of critical residues for viral entry and inhibition through structural Insight of HIV-1 fusion inhibitor CP621-652.
J.Biol.Chem., 287, 2012
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3VH7
 | | Structure of HIV-1 gp41 NHR/fusion inhibitor complex P21 | | 分子名称: | CP32M, Envelope glycoprotein gp160, MAGNESIUM ION | | 著者 | Yao, X, Waltersperger, S, Wang, M.T, Cui, S. | | 登録日 | 2011-08-23 | | 公開日 | 2012-06-13 | | 最終更新日 | 2023-11-08 | | 実験手法 | X-RAY DIFFRACTION (2.019 Å) | | 主引用文献 | Structural basis of potent and broad HIV-1 fusion inhibitor CP32M
J.Biol.Chem., 287, 2012
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5TTO
 | | X-ray crystal structure of PPARgamma in complex with SR1643 | | 分子名称: | 4-bromo-N-{3,5-dichloro-4-[(quinolin-3-yl)oxy]phenyl}-2,5-difluorobenzene-1-sulfonamide, Peroxisome proliferator-activated receptor gamma | | 著者 | Bruning, J.B, Frkic, R.L, Griffin, P, Kamenecka, T, Abell, A. | | 登録日 | 2016-11-04 | | 公開日 | 2017-05-24 | | 最終更新日 | 2023-10-04 | | 実験手法 | X-RAY DIFFRACTION (2.246 Å) | | 主引用文献 | Structure-Activity Relationship of 2,4-Dichloro-N-(3,5-dichloro-4-(quinolin-3-yloxy)phenyl)benzenesulfonamide (INT131) Analogs for PPAR gamma-Targeted Antidiabetics.
J. Med. Chem., 60, 2017
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7CSW
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7CSY
 | | Pseudomonas aeruginosa antitoxin HigA with higBA promoter | | 分子名称: | DNA (28-MER), DNA (29-MER), HTH cro/C1-type domain-containing protein, ... | | 著者 | Song, Y.J, Luo, G.H, Bao, R. | | 登録日 | 2020-08-17 | | 公開日 | 2021-01-13 | | 最終更新日 | 2024-05-29 | | 実験手法 | X-RAY DIFFRACTION (2.29 Å) | | 主引用文献 | Pseudomonas aeruginosa antitoxin HigA functions as a diverse regulatory factor by recognizing specific pseudopalindromic DNA motifs.
Environ.Microbiol., 23, 2021
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5BWA
 | | Crystal structure of ODC-PLP-AZ1 ternary complex | | 分子名称: | Ornithine decarboxylase, Ornithine decarboxylase antizyme 1, PYRIDOXAL-5'-PHOSPHATE | | 著者 | Wu, D.H. | | 登録日 | 2015-06-07 | | 公開日 | 2015-12-09 | | 最終更新日 | 2023-11-08 | | 実験手法 | X-RAY DIFFRACTION (3.2 Å) | | 主引用文献 | Structural basis of Ornithine Decarboxylase inactivation and accelerated degradation by polyamine sensor Antizyme1
Sci Rep, 5, 2015
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5CRL
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7CSV
 | | Pseudomonas aeruginosa antitoxin HigA | | 分子名称: | HTH cro/C1-type domain-containing protein | | 著者 | Song, Y.J, Luo, G.H, Bao, R. | | 登録日 | 2020-08-17 | | 公開日 | 2021-01-13 | | 最終更新日 | 2023-11-29 | | 実験手法 | X-RAY DIFFRACTION (1.71 Å) | | 主引用文献 | Pseudomonas aeruginosa antitoxin HigA functions as a diverse regulatory factor by recognizing specific pseudopalindromic DNA motifs.
Environ.Microbiol., 23, 2021
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8SDU
 | | Structure of rat organic anion transporter 1 (OAT1) | | 分子名称: | Solute carrier family 22 member 6 | | 著者 | Dou, T, Jiang, J. | | 登録日 | 2023-04-07 | | 公開日 | 2023-10-18 | | 最終更新日 | 2023-11-22 | | 実験手法 | ELECTRON MICROSCOPY (2.05 Å) | | 主引用文献 | The substrate and inhibitor binding mechanism of polyspecific transporter OAT1 revealed by high-resolution cryo-EM.
Nat.Struct.Mol.Biol., 30, 2023
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8SDZ
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8SDY
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8T53
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2IJM
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6NWS
 | | RORgamma Ligand Binding Domain | | 分子名称: | 2-chloro-6-fluoro-N-(1-{[3-(trifluoromethyl)phenyl]sulfonyl}-2,3-dihydro-1H-indol-6-yl)benzamide, Nuclear receptor ROR-gamma | | 著者 | Strutzenberg, T.S, Park, H.J, Griffin, P.R. | | 登録日 | 2019-02-07 | | 公開日 | 2019-07-10 | | 最終更新日 | 2023-10-11 | | 実験手法 | X-RAY DIFFRACTION (2.44 Å) | | 主引用文献 | HDX-MS reveals structural determinants for ROR gamma hyperactivation by synthetic agonists.
Elife, 8, 2019
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6NWU
 | | RORgamma Ligand Binding Domain | | 分子名称: | 6-[(3,5-dichloropyridin-4-yl)methoxy]-1-{[3-(trifluoromethyl)phenyl]sulfonyl}-2,3-dihydro-1H-indole, Nuclear receptor ROR-gamma | | 著者 | Strutzenberg, T.S, Park, H, Griffin, P.R. | | 登録日 | 2019-02-07 | | 公開日 | 2019-07-10 | | 最終更新日 | 2023-10-11 | | 実験手法 | X-RAY DIFFRACTION (3.2 Å) | | 主引用文献 | HDX-MS reveals structural determinants for ROR gamma hyperactivation by synthetic agonists.
Elife, 8, 2019
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