7SHW
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6VP9
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![BU of 6vp9 by Molmil](/molmil-images/mine/6vp9) | Cryo-EM structure of human NatB complex | 分子名称: | CARBOXYMETHYL COENZYME *A, MDVFM peptide, N-alpha-acetyltransferase 20, ... | 著者 | Deng, S, Marmorstein, R. | 登録日 | 2020-02-02 | 公開日 | 2020-09-23 | 最終更新日 | 2024-03-06 | 実験手法 | ELECTRON MICROSCOPY (3.46 Å) | 主引用文献 | Molecular basis for N-terminal alpha-synuclein acetylation by human NatB. Elife, 9, 2020
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7SCI
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![BU of 7sci by Molmil](/molmil-images/mine/7sci) | AM0627 metallopeptidase from Akkermansia muciniphila | 分子名称: | CHLORIDE ION, FORMIC ACID, Peptidase M60 domain-containing protein, ... | 著者 | Fernandez, D, Bertozzi, C.R, Shon, D.J. | 登録日 | 2021-09-28 | 公開日 | 2022-04-27 | 最終更新日 | 2023-10-18 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | Structure-guided mutagenesis of a mucin-selective metalloprotease from Akkermansia muciniphila alters substrate preferences. J.Biol.Chem., 298, 2022
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6VMD
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![BU of 6vmd by Molmil](/molmil-images/mine/6vmd) | Chloroplast ATP synthase (C1, CF1) | 分子名称: | ADENOSINE-5'-DIPHOSPHATE, ADENOSINE-5'-TRIPHOSPHATE, ATP synthase delta chain, ... | 著者 | Yang, J.-H, Williams, D, Kandiah, E, Fromme, P, Chiu, P.-L. | 登録日 | 2020-01-27 | 公開日 | 2020-09-09 | 最終更新日 | 2020-09-16 | 実験手法 | ELECTRON MICROSCOPY (4.53 Å) | 主引用文献 | Structural basis of redox modulation on chloroplast ATP synthase. Commun Biol, 3, 2020
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6VMG
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![BU of 6vmg by Molmil](/molmil-images/mine/6vmg) | Chloroplast ATP synthase (O3, CF1FO) | 分子名称: | ATP synthase delta chain, chloroplastic, ATP synthase epsilon chain, ... | 著者 | Yang, J.-H, Williams, D, Kandiah, E, Fromme, P, Chiu, P.-L. | 登録日 | 2020-01-27 | 公開日 | 2020-09-09 | 最終更新日 | 2024-03-06 | 実験手法 | ELECTRON MICROSCOPY (6.46 Å) | 主引用文献 | Structural basis of redox modulation on chloroplast ATP synthase. Commun Biol, 3, 2020
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3BRK
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3C2I
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![BU of 3c2i by Molmil](/molmil-images/mine/3c2i) | The Crystal Structure of Methyl-CpG Binding Domain of Human MeCP2 in Complex with a Methylated DNA Sequence from BDNF | 分子名称: | DNA (5'-D(*DAP*DTP*DAP*DGP*DAP*DAP*DGP*DAP*DAP*DTP*DTP*DCP*(5CM)P*DGP*DTP*DTP*DCP*DCP*DAP*DG)-3'), DNA (5'-D(*DTP*DCP*DTP*DGP*DGP*DAP*DAP*(5CM)P*DGP*DGP*DAP*DAP*DTP*DTP*DCP*DTP*DTP*DCP*DTP*DA)-3'), Methyl-CpG-binding protein 2 | 著者 | Ho, K.L, McNae, I.W, Schmiedeberg, L, Klose, R.J, Bird, A.P, Walkinshaw, M.D. | 登録日 | 2008-01-25 | 公開日 | 2008-05-13 | 最終更新日 | 2021-11-10 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | MeCP2 binding to DNA depends upon hydration at methyl-CpG Mol.Cell, 29, 2008
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8Q68
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![BU of 8q68 by Molmil](/molmil-images/mine/8q68) | Crystal structure of TEAD1-YBD in complex with irreversible compound SWTX-143 | 分子名称: | Transcriptional enhancer factor TEF-1, ~{N}-[(3~{S})-5-azanyl-1-[4-(trifluoromethyl)phenyl]-3,4-dihydro-2~{H}-quinolin-3-yl]propanamide | 著者 | Ciesielski, F, Spieser, S.A.H, Marchand, A, Gwaltney, S.L. | 登録日 | 2023-08-11 | 公開日 | 2023-10-04 | 最終更新日 | 2024-01-17 | 実験手法 | X-RAY DIFFRACTION (1.58 Å) | 主引用文献 | A Novel Irreversible TEAD Inhibitor, SWTX-143, Blocks Hippo Pathway Transcriptional Output and Causes Tumor Regression in Preclinical Mesothelioma Models. Mol.Cancer Ther., 23, 2024
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3C6A
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3BY9
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7S2V
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3C9B
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![BU of 3c9b by Molmil](/molmil-images/mine/3c9b) | Crystal structure of SeMet Vps75 | 分子名称: | Vacuolar protein sorting-associated protein 75 | 著者 | Keck, J.L, Berndsen, C.E, Tsubota, T, Lindner, S.E, Lee, S, Holton, J.M, Kaufman, P.D, Denu, J.M. | 登録日 | 2008-02-15 | 公開日 | 2008-08-12 | 最終更新日 | 2011-07-13 | 実験手法 | X-RAY DIFFRACTION (2.42 Å) | 主引用文献 | Molecular functions of the histone acetyltransferase chaperone complex Rtt109-Vps75 Nat.Struct.Mol.Biol., 15, 2008
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7SET
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![BU of 7set by Molmil](/molmil-images/mine/7set) | SARS-CoV-2 Main Protease (Mpro) in Complex with ML1000 | 分子名称: | (1R,2S,5S)-N-{(2S,3R)-4-amino-3-hydroxy-4-oxo-1-[(3S)-2-oxopyrrolidin-3-yl]butan-2-yl}-3-[N-(tert-butylcarbamoyl)-3-methyl-L-valyl]-6,6-dimethyl-3-azabicyclo[3.1.0]hexane-2-carboxamide, 3C-like proteinase, CHLORIDE ION | 著者 | Westberg, M, Fernandez, D, Lin, M.Z. | 登録日 | 2021-10-01 | 公開日 | 2022-10-05 | 最終更新日 | 2024-04-17 | 実験手法 | X-RAY DIFFRACTION (1.7 Å) | 主引用文献 | An orally bioavailable SARS-CoV-2 main protease inhibitor exhibits improved affinity and reduced sensitivity to mutations. Sci Transl Med, 16, 2024
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7S2A
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7S29
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7S2F
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7S2C
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7S2G
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7S30
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7S33
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7S28
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7S2D
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7S2B
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7S32
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7S34
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