8FXQ
| The Crystal Sturucture of Rhizopuspepsin with a bound modified peptide inhibitor generated by de novo drug design. | 分子名称: | ALA-CYS-VAL-LYS, CYCLOHEXANE, Rhizopuspepsin, ... | 著者 | Satyshur, K.A, Rich, D.H, Ripka, A.S. | 登録日 | 2023-01-25 | 公開日 | 2023-02-08 | 最終更新日 | 2024-10-09 | 実験手法 | X-RAY DIFFRACTION (1.21 Å) | 主引用文献 | Aspartic protease inhibitors designed from computer-generated templates bind as predicted. Org Lett, 3, 2001
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8HS8
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7BB8
| Crystal structure of Lugdulysin, a Staphylococcus lugdunensis M30 zinc metallopeptidase | 分子名称: | ACETATE ION, CACODYLATE ION, CALCIUM ION, ... | 著者 | Ruff, M, Prevost, G, Prola, K, Levy, N. | 登録日 | 2020-12-17 | 公開日 | 2022-07-13 | 最終更新日 | 2024-06-19 | 実験手法 | X-RAY DIFFRACTION (1.506 Å) | 主引用文献 | Crystal structure of Staphylococcus lugdunensis protease, Lugdulysin To Be Published
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7BLF
| Crystal structure of ene-reductase OYE4 from Botryotinia fuckeliana (BfOYE4) | 分子名称: | FLAVIN MONONUCLEOTIDE, FORMIC ACID, Oxidored_FMN domain-containing protein | 著者 | Robescu, M.S, Bergantino, E, Hall, M, Cendron, L. | 登録日 | 2021-01-18 | 公開日 | 2022-07-13 | 最終更新日 | 2024-01-31 | 実験手法 | X-RAY DIFFRACTION (2.15 Å) | 主引用文献 | Asymmetric Proton Transfer Catalysis by Stereocomplementary Old Yellow Enzymes for C=C Bond Isomerization Reaction Acs Catalysis, 12, 2022
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7BN6
| Crystal structure of G. sulphuraria ene-reductase GsOYE in complex with b-angelica lactone | 分子名称: | (2~{R})-2-methyl-2~{H}-furan-5-one, FLAVIN MONONUCLEOTIDE, NADPH2 dehydrogenase-like protein | 著者 | Robescu, M.S, Bergantino, E, Hall, M, Cendron, L. | 登録日 | 2021-01-21 | 公開日 | 2022-07-13 | 最終更新日 | 2024-01-31 | 実験手法 | X-RAY DIFFRACTION (1.5 Å) | 主引用文献 | Asymmetric Proton Transfer Catalysis by Stereocomplementary Old Yellow Enzymes for C=C Bond Isomerization Reaction Acs Catalysis, 12, 2022
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7BHD
| FimH in complex with alpha1,6 core-fucosylated oligomannose-3, crystallized in the trigonal space group | 分子名称: | NICKEL (II) ION, SULFATE ION, Type 1 fimbrin D-mannose specific adhesin, ... | 著者 | Bridot, C, Bouckaert, J, Krammer, E.-M. | 登録日 | 2021-01-11 | 公開日 | 2022-07-20 | 最終更新日 | 2024-02-07 | 実験手法 | X-RAY DIFFRACTION (1.4 Å) | 主引用文献 | Structural insights into a cooperative switch between one and two FimH bacterial adhesins binding pauci- and high-mannose type N-glycan receptors. J.Biol.Chem., 299, 2023
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8FV1
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8I3E
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8FJD
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8FZK
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8FNU
| Structure of RdrA from Streptococcus suis RADAR defense system | 分子名称: | KAP NTPase domain-containing protein | 著者 | Duncan-Lowey, B, Johnson, A.G, Rawson, S, Mayer, M.L, Kranzusch, P.J. | 登録日 | 2022-12-28 | 公開日 | 2023-02-01 | 最終更新日 | 2024-06-19 | 実験手法 | ELECTRON MICROSCOPY (2.5 Å) | 主引用文献 | Cryo-EM structure of the RADAR supramolecular anti-phage defense complex. Cell, 186, 2023
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8HVU
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8FDP
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8HZR
| Crystal structure of SARS-Cov-2 main protease S46F mutant in complex with PF07321332 | 分子名称: | (1R,2S,5S)-N-{(1E,2S)-1-imino-3-[(3S)-2-oxopyrrolidin-3-yl]propan-2-yl}-6,6-dimethyl-3-[3-methyl-N-(trifluoroacetyl)-L-valyl]-3-azabicyclo[3.1.0]hexane-2-carboxamide, 3C-like proteinase nsp5 | 著者 | Zeng, X.Y, Zhang, J, Li, J. | 登録日 | 2023-01-09 | 公開日 | 2024-01-17 | 実験手法 | X-RAY DIFFRACTION (1.92 Å) | 主引用文献 | Crystal structure of SARS-Cov-2 main protease
S46F mutant in complex with PF07321332 To Be Published
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8F94
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8HVX
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8FDR
| Structure of a dodecamer complex: 5'-CGCGAAAAGCCG-3-DB1476 | 分子名称: | 4,4'-(1H-benzimidazole-2,6-diyl)di(benzene-1-carboximidamide), DNA (5'-D(*CP*GP*CP*GP*AP*AP*AP*AP*CP*GP*CP*G)-3'), DNA (5'-D(*CP*GP*CP*GP*TP*TP*TP*TP*CP*GP*CP*G)-3'), ... | 著者 | Ogbonna, E, Wilson, W.D. | 登録日 | 2022-12-04 | 公開日 | 2023-02-22 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (1.55 Å) | 主引用文献 | X-ray Structure Characterization of the Selective Recognition of AT Base Pair Sequences. Acs Bio Med Chem Au, 3, 2023
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8I2N
| The RIPK1 kinase domain in complex with QY7-2B compound | 分子名称: | Receptor-interacting serine/threonine-protein kinase 1, ~{N}-methyl-1-[4-[[[1-methyl-5-(phenylmethyl)pyrazol-3-yl]carbonylamino]methyl]phenyl]benzimidazole-5-carboxamide | 著者 | Gong, X.Y, Li, Y, Meng, H.Y, Pan, L.F. | 登録日 | 2023-01-14 | 公開日 | 2024-01-31 | 最終更新日 | 2024-08-21 | 実験手法 | X-RAY DIFFRACTION (2.29 Å) | 主引用文献 | Structure-based development of potent and selective type-II kinase inhibitors of RIPK1. Acta Pharm Sin B, 14, 2024
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8HVV
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8FG7
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7C2Y
| The crystal structure of COVID-2019 main protease in the apo state | 分子名称: | 3C-like proteinase | 著者 | Zhou, X.L, Zhong, F.L, Lin, C, Zhou, H, Hu, X.H, Wang, Q.S, Li, J, Zhang, J. | 登録日 | 2020-05-10 | 公開日 | 2020-09-02 | 最終更新日 | 2023-11-29 | 実験手法 | X-RAY DIFFRACTION (1.91 Å) | 主引用文献 | COVID-2019 main protease in the apo state To Be Published
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7C3I
| Structure of L-lysine oxidase D212A/D315A | 分子名称: | 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID, FLAVIN-ADENINE DINUCLEOTIDE, GLYCEROL, ... | 著者 | Kitagawa, M, Matsumoto, Y, Inagaki, K, Imada, K. | 登録日 | 2020-05-12 | 公開日 | 2020-09-23 | 最終更新日 | 2023-11-29 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Structural basis of strict substrate recognition of l-lysine alpha-oxidase from Trichoderma viride. Protein Sci., 29, 2020
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7C51
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8HS7
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7C6S
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