6N2L
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6NBO
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6NDR
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6Q1Y
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5J6B
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5IV9
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![BU of 5iv9 by Molmil](/molmil-images/mine/5iv9) | The LPS Transporter LptDE from Klebsiella pneumoniae, full-length | Descriptor: | (HYDROXYETHYLOXY)TRI(ETHYLOXY)OCTANE, LPS-assembly lipoprotein LptE, LPS-assembly protein LptD | Authors: | Botos, I, McCarthy, J.G, Buchanan, S.K. | Deposit date: | 2016-03-20 | Release date: | 2016-05-18 | Last modified: | 2016-06-15 | Method: | X-RAY DIFFRACTION (4.369 Å) | Cite: | Structural and Functional Characterization of the LPS Transporter LptDE from Gram-Negative Pathogens. Structure, 24, 2016
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6OE6
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6NCR
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5IDU
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6O49
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5IF3
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6ULO
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4ZDQ
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6EEP
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7ZJ6
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![BU of 7zj6 by Molmil](/molmil-images/mine/7zj6) | X-31 Hemagglutinin Precursor HA0 at pH 7.5 | Descriptor: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, Hemagglutinin,Fibritin, ... | Authors: | Garcia-Moro, E, Rosenthal, P.B. | Deposit date: | 2022-04-08 | Release date: | 2022-08-17 | Method: | ELECTRON MICROSCOPY (2.6 Å) | Cite: | Reversible structural changes in the influenza hemagglutinin precursor at membrane fusion pH. Proc.Natl.Acad.Sci.USA, 119, 2022
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7ZJ7
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![BU of 7zj7 by Molmil](/molmil-images/mine/7zj7) | X-31 Hemagglutinin Precursor HA0 at pH 4.8 | Descriptor: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, Hemagglutinin,Fibritin, ... | Authors: | Garcia-Moro, E, Rosenthal, P.B. | Deposit date: | 2022-04-08 | Release date: | 2022-08-17 | Method: | ELECTRON MICROSCOPY (3.95 Å) | Cite: | Reversible structural changes in the influenza hemagglutinin precursor at membrane fusion pH. Proc.Natl.Acad.Sci.USA, 119, 2022
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7ZJ8
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![BU of 7zj8 by Molmil](/molmil-images/mine/7zj8) | X-31 Hemagglutinin Precursor HA0 at pH 7.5 after reneutralization | Descriptor: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, Hemagglutinin,Fibritin, ... | Authors: | Garcia-Moro, E, Rosenthal, P.B. | Deposit date: | 2022-04-08 | Release date: | 2022-08-17 | Method: | ELECTRON MICROSCOPY (3.1 Å) | Cite: | Reversible structural changes in the influenza hemagglutinin precursor at membrane fusion pH. Proc.Natl.Acad.Sci.USA, 119, 2022
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5LS6
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![BU of 5ls6 by Molmil](/molmil-images/mine/5ls6) | Structure of Human Polycomb Repressive Complex 2 (PRC2) with inhibitor | Descriptor: | 1-[(1~{R})-1-[1-[2,2-bis(fluoranyl)propyl]piperidin-4-yl]ethyl]-~{N}-[(4-methoxy-6-methyl-2-oxidanylidene-3~{H}-pyridin-3-yl)methyl]-2-methyl-indole-3-carboxamide, Histone-lysine N-methyltransferase EZH2,Histone-lysine N-methyltransferase EZH2,Histone-lysine N-methyltransferase EZH2, Jarid2 K116me3, ... | Authors: | Zhang, Y, Justin, N, Chen, S, Wilson, J, Gamblin, S. | Deposit date: | 2016-08-22 | Release date: | 2017-02-22 | Last modified: | 2024-01-17 | Method: | X-RAY DIFFRACTION (3.47 Å) | Cite: | Identification of (R)-N-((4-Methoxy-6-methyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methyl-1-(1-(1-(2,2,2-trifluoroethyl)piperidin-4-yl)ethyl)-1H-indole-3-carboxamide (CPI-1205), a Potent and Selective Inhibitor of Histone Methyltransferase EZH2, Suitable for Phase I Clinical Trials for B-Cell Lymphomas. J. Med. Chem., 59, 2016
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4RGB
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![BU of 4rgb by Molmil](/molmil-images/mine/4rgb) | |
5M5G
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![BU of 5m5g by Molmil](/molmil-images/mine/5m5g) | Crystal structure of the Chaetomium Thermophilum polycomb repressive complex 2 (PRC2) | Descriptor: | Fragment from molecular 2 (region containing putative polycomb protein Suz12), HISTONE H3 11-Mer peptide, Putative uncharacterized protein, ... | Authors: | Zhang, Y, Justin, N, Wilson, J, Gamblin, S. | Deposit date: | 2016-10-21 | Release date: | 2017-01-11 | Last modified: | 2019-10-16 | Method: | X-RAY DIFFRACTION (2.27 Å) | Cite: | Comment on "Structural basis of histone H3K27 trimethylation by an active polycomb repressive complex 2". Science, 354, 2016
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5WOQ
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6MOM
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![BU of 6mom by Molmil](/molmil-images/mine/6mom) | Crystal structure of human Interleukin-1 receptor associated Kinase 4 (IRAK 4, CID 100300) in complex with compound NCC00371481 (BSI 107591) | Descriptor: | 1,2-ETHANEDIOL, 6-[7-methoxy-6-(1-methyl-1H-pyrazol-4-yl)imidazo[1,2-a]pyridin-3-yl]-N-[(3R)-pyrrolidin-3-yl]pyridin-2-amine, Interleukin-1 receptor-associated kinase 4 | Authors: | Abendroth, J, Mayclin, S.J, Lorimer, D.D, Starczynowski, D, Hoyt, S, Tawa, G, Thomas, C. | Deposit date: | 2018-10-04 | Release date: | 2019-10-16 | Last modified: | 2023-10-11 | Method: | X-RAY DIFFRACTION (2.1 Å) | Cite: | Overcoming adaptive therapy resistance in AML by targeting immune response pathways. Sci Transl Med, 11, 2019
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5KWV
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5BT9
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8DT1
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![BU of 8dt1 by Molmil](/molmil-images/mine/8dt1) | |