4KY8
| Crystal structure of TS-DHFR from Cryptosporidium hominis in complex with NADPH, methotrexate, FdUMP and 4-((2-amino-6-methyl-4-oxo-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimidin-5-yl)thio)-2-chlorophenyl)-L-glutamic acid | 分子名称: | 5-FLUORO-2'-DEOXYURIDINE-5'-MONOPHOSPHATE, Bifunctional thymidylate synthase-dihydrofolate reductase, METHOTREXATE, ... | 著者 | Kumar, V.P, Anderson, K.S. | 登録日 | 2013-05-28 | 公開日 | 2013-08-21 | 最終更新日 | 2023-09-20 | 実験手法 | X-RAY DIFFRACTION (3.084 Å) | 主引用文献 | Substituted pyrrolo[2,3-d]pyrimidines as Cryptosporidium hominis thymidylate synthase inhibitors. Bioorg.Med.Chem.Lett., 23, 2013
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4MBI
| Discovery of Pyrazolo[1,5a]pyrimidine-based Pim1 Inhibitors | 分子名称: | N,N-dimethyl-N'-[3-(1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrimidin-5-yl]ethane-1,2-diamine, Serine/threonine-protein kinase pim-1 | 著者 | Azevedo, R, Fischmann, T.O. | 登録日 | 2013-08-19 | 公開日 | 2013-09-18 | 最終更新日 | 2024-02-28 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Discovery of pyrazolo[1,5-a]pyrimidine-based Pim inhibitors: A template-based approach. Bioorg.Med.Chem.Lett., 23, 2013
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7BFZ
| X-ray structure of human prostate-specific membrane antigen(PSMA) in complex with a inhibitor Glu-490 | 分子名称: | (((S)-1-carboxy-5-((E)-2-cyano-3-(5-(1-(3-methoxy-3-oxopropyl)-1,2,3,4-tetrahydroquinolin-6-yl)thiophen-2-yl)acrylamido)pentyl)carbamoyl)-L-glutamic acid, 1,2-ETHANEDIOL, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... | 著者 | Rakhimbekova, A, Motlova, L, Barinka, C. | 登録日 | 2021-01-05 | 公開日 | 2021-08-18 | 最終更新日 | 2024-01-31 | 実験手法 | X-RAY DIFFRACTION (1.73 Å) | 主引用文献 | A prostate-specific membrane antigen activated molecular rotor for real-time fluorescence imaging. Nat Commun, 12, 2021
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8IXZ
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7DRW
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8IY1
| Structure of Acb2 complexed with cAAG | 分子名称: | GUANOSINE-3'-MONOPHOSPHATE, [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] dihydrogen phosphate, p26 | 著者 | Cao, X.L, Xiao, Y, Feng, Y. | 登録日 | 2023-04-03 | 公開日 | 2024-02-07 | 最終更新日 | 2024-03-13 | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | 主引用文献 | Phage anti-CBASS protein simultaneously sequesters cyclic trinucleotides and dinucleotides. Mol.Cell, 84, 2024
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4MBL
| Discovery of Pyrazolo[1,5a]pyrimidine-based Pim1 Inhibitors | 分子名称: | (1R,2R)-N-[3-(naphthalen-2-yl)pyrazolo[1,5-a]pyrimidin-5-yl]cyclohexane-1,2-diamine, Serine/threonine-protein kinase pim-1 | 著者 | Azevedo, R, Fischmann, T.O. | 登録日 | 2013-08-19 | 公開日 | 2013-09-11 | 最終更新日 | 2024-02-28 | 実験手法 | X-RAY DIFFRACTION (2.6 Å) | 主引用文献 | Discovery of pyrazolo[1,5-a]pyrimidine-based Pim inhibitors: A template-based approach. Bioorg.Med.Chem.Lett., 23, 2013
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7C96
| Avr1d:GmPUB13 U-box | 分子名称: | RING-type E3 ubiquitin transferase, RxLR effector protein Avh6 | 著者 | Xing, W, Hu, Q, Zhou, J, Yao, D. | 登録日 | 2020-06-05 | 公開日 | 2021-03-17 | 実験手法 | X-RAY DIFFRACTION (2.51 Å) | 主引用文献 | Phytophthora sojae effector Avr1d functions as an E2 competitor and inhibits ubiquitination activity of GmPUB13 to facilitate infection. Proc.Natl.Acad.Sci.USA, 118, 2021
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6JEB
| crystal structure of a beta-N-acetylhexosaminidase | 分子名称: | ACETAMIDE, Beta-N-acetylhexosaminidase, ZINC ION | 著者 | Chen, X, Wang, J.C, Liu, M.J, Yang, W.Y, Wang, Y.Z, Tang, R.P, Zhang, M. | 登録日 | 2019-02-05 | 公開日 | 2019-03-13 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (1.498 Å) | 主引用文献 | Crystallographic evidence for substrate-assisted catalysis of beta-N-acetylhexosaminidas from Akkermansia muciniphila. Biochem. Biophys. Res. Commun., 511, 2019
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8H59
| A fungal MAP kinase in complex with an inhibitor | 分子名称: | Mitogen-activated protein kinase MPS1, ~{N}-[(2~{S})-3-(1~{H}-indol-3-yl)-1-(methylamino)-1-oxidanylidene-propan-2-yl]-8-[2-methoxy-5-(trifluoromethyloxy)phenyl]-1,6-naphthyridine-2-carboxamide | 著者 | Kong, Z, Zhang, X, Wang, D, Liu, J. | 登録日 | 2022-10-12 | 公開日 | 2023-02-08 | 最終更新日 | 2023-11-29 | 実験手法 | X-RAY DIFFRACTION (2.15 Å) | 主引用文献 | Structure-Aided Identification of an Inhibitor Targets Mps1 for the Management of Plant-Pathogenic Fungi. Mbio, 14, 2023
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8HE1
| The structure of chitin deacetylase Pst_13661 from Puccinia striiformis f. sp. tritici | 分子名称: | BENZHYDROXAMIC ACID, Chitin deacetylase, ZINC ION | 著者 | Liu, L, Li, Y.C, Zhou, Y, Yang, Q. | 登録日 | 2022-11-07 | 公開日 | 2023-05-31 | 最終更新日 | 2023-11-29 | 実験手法 | X-RAY DIFFRACTION (1.61 Å) | 主引用文献 | Inhibition of chitin deacetylases to attenuate plant fungal diseases. Nat Commun, 14, 2023
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8HFA
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8HF9
| The structure of chitin deacetylase Pst_13661 from Puccinia striiformis f. sp. tritici | 分子名称: | Chitin deacetylase, ZINC ION | 著者 | Liu, L, Li, Y.C, Zhou, Y, Yang, Q. | 登録日 | 2022-11-10 | 公開日 | 2023-05-31 | 最終更新日 | 2024-10-09 | 実験手法 | X-RAY DIFFRACTION (1.96 Å) | 主引用文献 | Inhibition of chitin deacetylases to attenuate plant fungal diseases. Nat Commun, 14, 2023
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5YO5
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5YOE
| Crystal Structure of flavodoxin with engineered disulfide bond A43C-L74C | 分子名称: | FLAVIN MONONUCLEOTIDE, Flavodoxin, GLYCEROL | 著者 | Pu, M, Xu, Z, Song, G, Liu, Z.J. | 登録日 | 2017-10-27 | 公開日 | 2017-12-27 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (1.35 Å) | 主引用文献 | Protein crystal quality oriented disulfide bond engineering. Protein Cell, 9, 2018
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5YM7
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5YO6
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5YO3
| Crystal Structure of B562RIL with engineered disulfide bond V16C-A29C | 分子名称: | SULFATE ION, Soluble cytochrome b562 | 著者 | Pu, M, Xu, Z, Song, G, Liu, Z.J. | 登録日 | 2017-10-26 | 公開日 | 2018-05-09 | 最終更新日 | 2024-10-09 | 実験手法 | X-RAY DIFFRACTION (1.7 Å) | 主引用文献 | Protein crystal quality oriented disulfide bond engineering. Protein Cell, 9, 2018
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5YOB
| Crystal Structure of flavodoxin without engineered disulfide bond | 分子名称: | FLAVIN MONONUCLEOTIDE, Flavodoxin, GLYCEROL | 著者 | Pu, M, Xu, Z, Song, G, Liu, Z.J. | 登録日 | 2017-10-27 | 公開日 | 2017-12-27 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (1.142 Å) | 主引用文献 | Protein crystal quality oriented disulfide bond engineering. Protein Cell, 9, 2018
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5YT4
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8XNG
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8XVZ
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8XS4
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8XVX
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8XS0
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