8H5S
 
 | Crystal structure of Rv3400 from Mycobacterium tuberculosis | 分子名称: | 1,2-ETHANEDIOL, Beta-phosphoglucomutase, CHLORIDE ION, ... | 著者 | Singh, L, Karthikeyan, S, Thakur, K.G. | 登録日 | 2022-10-13 | 公開日 | 2023-10-25 | 最終更新日 | 2024-11-06 | 実験手法 | X-RAY DIFFRACTION (1.7 Å) | 主引用文献 | Biochemical and structural characterization reveals Rv3400 codes for beta-phosphoglucomutase in Mycobacterium tuberculosis. Protein Sci., 33, 2024
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7YK3
 
 | Crystal structure of DarTG toxin-antitoxin complex from Mycobacterium tuberculosis | 分子名称: | DNA ADP-ribosyl glycohydrolase, DNA ADP-ribosyl transferase, PHOSPHATE ION | 著者 | Deep, A, Kaur, J, Singh, L, Thakur, K.G. | 登録日 | 2022-07-21 | 公開日 | 2023-05-31 | 最終更新日 | 2024-12-18 | 実験手法 | X-RAY DIFFRACTION (2.2 Å) | 主引用文献 | Structural insights into DarT toxin neutralization by cognate DarG antitoxin: ssDNA mimicry by DarG C-terminal domain keeps the DarT toxin inhibited. Structure, 31, 2023
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5EC5
 
 | Crystal structure of lysenin pore | 分子名称: | Lysenin, MERCURIBENZOIC ACID, MERCURY (II) ION | 著者 | Podobnik, M, Savory, P, Rojko, N, Kisovec, M, Bruce, M, Jayasinghe, L, Anderluh, G. | 登録日 | 2015-10-20 | 公開日 | 2016-05-18 | 最終更新日 | 2024-05-08 | 実験手法 | X-RAY DIFFRACTION (3.1 Å) | 主引用文献 | Crystal structure of an invertebrate cytolysin pore reveals unique properties and mechanism of assembly. Nat Commun, 7, 2016
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6SI7
 
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4X7Q
 
 | PIM2 kinase in complex with Compound 1s | 分子名称: | 2-(2,6-difluorophenyl)-N-{4-[(3S)-pyrrolidin-3-yloxy]pyridin-3-yl}-1,3-thiazole-4-carboxamide, PHOSPHATE ION, Serine/threonine-protein kinase pim-2 | 著者 | Marcotte, D.J, Silvian, L.F. | 登録日 | 2014-12-09 | 公開日 | 2015-02-11 | 最終更新日 | 2023-09-27 | 実験手法 | X-RAY DIFFRACTION (2.33 Å) | 主引用文献 | Structure-based design of low-nanomolar PIM kinase inhibitors. Bioorg.Med.Chem.Lett., 25, 2015
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4XHK
 
 | PIM1 kinase in complex with Compound 1s | 分子名称: | 2-(2,6-difluorophenyl)-N-{4-[(3S)-pyrrolidin-3-yloxy]pyridin-3-yl}-1,3-thiazole-4-carboxamide, Serine/threonine-protein kinase pim-1 | 著者 | Marcotte, D.J, Silvian, L.F. | 登録日 | 2015-01-05 | 公開日 | 2015-02-11 | 最終更新日 | 2024-10-16 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | Structure-based design of low-nanomolar PIM kinase inhibitors. Bioorg.Med.Chem.Lett., 25, 2015
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8GC1
 
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8GBZ
 
 | Crystal structure of PC39-55C, an anti-HIV broadly neutralizing antibody | 分子名称: | DI(HYDROXYETHYL)ETHER, PC39-55C Fab heavy chain, PC39-55C Fab light chain | 著者 | Murrell, S, Omorodion, O, Wilson, I.A. | 登録日 | 2023-02-28 | 公開日 | 2023-06-07 | 最終更新日 | 2024-10-23 | 実験手法 | X-RAY DIFFRACTION (1.97 Å) | 主引用文献 | Antigen pressure from two founder viruses induces multiple insertions at a single antibody position to generate broadly neutralizing HIV antibodies. Plos Pathog., 19, 2023
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4GXS
 
 | Ligand binding domain of GluA2 (AMPA/glutamate receptor) bound to (-)-kaitocephalin | 分子名称: | (5R)-2-[(1S,2R)-2-amino-2-carboxy-1-hydroxyethyl]-5-{(2S)-2-carboxy-2-[(3,5-dichloro-4-hydroxybenzoyl)amino]ethyl}-L-proline, Glutamate receptor 2, ZINC ION | 著者 | Ahmed, A.H, Oswald, R.E. | 登録日 | 2012-09-04 | 公開日 | 2012-10-17 | 最終更新日 | 2024-11-06 | 実験手法 | X-RAY DIFFRACTION (1.9634 Å) | 主引用文献 | The structure of (-)-kaitocephalin bound to the ligand binding domain of the (S)-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)/glutamate receptor, GluA2. J.Biol.Chem., 287, 2012
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