7LK3
| Crystal structure of untwinned human GABARAPL2 | 分子名称: | 1,2-ETHANEDIOL, Gamma-aminobutyric acid receptor-associated protein-like 2 | 著者 | Scicluna, K, Dewson, G, Czabotar, P.E, Birkinshaw, R.W. | 登録日 | 2021-02-01 | 公開日 | 2021-05-12 | 最終更新日 | 2023-10-18 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | A new crystal form of GABARAPL2. Acta Crystallogr.,Sect.F, 77, 2021
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7T3X
| Structure of unphosphorylated Pediculus humanus (Ph) PINK1 D334A mutant | 分子名称: | Serine/threonine-protein kinase PINK1 | 著者 | Gan, Z.Y, Leis, A, Dewson, G, Glukhova, A, Komander, D. | 登録日 | 2021-12-09 | 公開日 | 2021-12-22 | 最終更新日 | 2023-10-18 | 実験手法 | X-RAY DIFFRACTION (3.53 Å) | 主引用文献 | Activation mechanism of PINK1. Nature, 602, 2022
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7T4K
| Structure of dimeric phosphorylated Pediculus humanus (Ph) PINK1 with kinked alpha-C helix in chain B | 分子名称: | Serine/threonine-protein kinase PINK1, putative | 著者 | Gan, Z.Y, Leis, A, Dewson, G, Glukhova, A, Komander, D. | 登録日 | 2021-12-10 | 公開日 | 2022-01-12 | 最終更新日 | 2024-10-16 | 実験手法 | ELECTRON MICROSCOPY (3.25 Å) | 主引用文献 | Activation mechanism of PINK1. Nature, 602, 2022
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7T4N
| Structure of dimeric unphosphorylated Pediculus humanus (Ph) PINK1 D357A mutant | 分子名称: | Serine/threonine-protein kinase PINK1, putative | 著者 | Gan, Z.Y, Leis, A, Dewson, G, Glukhova, A, Komander, D. | 登録日 | 2021-12-10 | 公開日 | 2022-01-12 | 最終更新日 | 2024-02-28 | 実験手法 | ELECTRON MICROSCOPY (2.35 Å) | 主引用文献 | Activation mechanism of PINK1. Nature, 602, 2022
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7T4L
| Structure of dimeric phosphorylated Pediculus humanus (Ph) PINK1 with extended alpha-C helix in chain B | 分子名称: | Serine/threonine-protein kinase PINK1, putative | 著者 | Gan, Z.Y, Leis, A, Dewson, G, Glukhova, A, Komander, D. | 登録日 | 2021-12-10 | 公開日 | 2022-01-12 | 最終更新日 | 2024-10-09 | 実験手法 | ELECTRON MICROSCOPY (3.28 Å) | 主引用文献 | Activation mechanism of PINK1. Nature, 602, 2022
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7T4M
| Structure of dodecameric unphosphorylated Pediculus humanus (Ph) PINK1 D357A mutant | 分子名称: | Serine/threonine-protein kinase PINK1, putative | 著者 | Gan, Z.Y, Leis, A, Dewson, G, Glukhova, A, Komander, D. | 登録日 | 2021-12-10 | 公開日 | 2022-01-12 | 最終更新日 | 2024-02-28 | 実験手法 | ELECTRON MICROSCOPY (2.48 Å) | 主引用文献 | Activation mechanism of PINK1. Nature, 602, 2022
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4ZIE
| Crystal Structure of core/latch dimer of Bax in complex with BimBH3 | 分子名称: | 1,2-ETHANEDIOL, Apoptosis regulator BAX, Bcl-2-like protein 11 | 著者 | Krishna Kumar, K, Robin, A.Y, Westphal, D, Wardak, A.Z, Thompson, G.V, Dewson, G, Colman, P.M, Czabotar, P.E. | 登録日 | 2015-04-28 | 公開日 | 2015-07-22 | 最終更新日 | 2023-09-27 | 実験手法 | X-RAY DIFFRACTION (1.797 Å) | 主引用文献 | Crystal structure of Bax bound to the BH3 peptide of Bim identifies important contacts for interaction. Cell Death Dis, 6, 2015
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4ZIF
| Crystal Structure of core/latch dimer of Bax in complex with BimBH3mini | 分子名称: | Apoptosis regulator BAX, Bcl-2-like protein 11 | 著者 | Robin, A.Y, Krishna Kumar, K, Westphal, D, Wardak, A.Z, Thompson, G.V, Dewson, G, Colman, P.M, Czabotar, P.E. | 登録日 | 2015-04-28 | 公開日 | 2015-07-22 | 最終更新日 | 2023-09-27 | 実験手法 | X-RAY DIFFRACTION (2.401 Å) | 主引用文献 | Crystal structure of Bax bound to the BH3 peptide of Bim identifies important contacts for interaction. Cell Death Dis, 6, 2015
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4ZII
| Crystal Structure of core/latch dimer of BaxI66A in complex with BidBH3 | 分子名称: | 1,2-ETHANEDIOL, Apoptosis regulator BAX, BH3-interacting domain death agonist | 著者 | Czabotar, P.E, Robin, A.Y, Krishna Kumar, K, Westphal, D, Wardak, A.Z, Thompson, G.V, Dewson, G, Colman, P.M. | 登録日 | 2015-04-28 | 公開日 | 2015-07-22 | 最終更新日 | 2023-09-27 | 実験手法 | X-RAY DIFFRACTION (2.191 Å) | 主引用文献 | Crystal structure of Bax bound to the BH3 peptide of Bim identifies important contacts for interaction. Cell Death Dis, 6, 2015
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4ZIG
| Crystal Structure of core/latch dimer of Bax in complex with BidBH3mini | 分子名称: | Apoptosis regulator BAX, BH3-interacting domain death agonist | 著者 | Robin, A.Y, Krishna Kumar, K, Westphal, D, Wardak, A.Z, Thompson, G.V, Dewson, G, Colman, P.M, Czabotar, P.E. | 登録日 | 2015-04-28 | 公開日 | 2015-07-22 | 最終更新日 | 2023-09-27 | 実験手法 | X-RAY DIFFRACTION (2.2 Å) | 主引用文献 | Crystal structure of Bax bound to the BH3 peptide of Bim identifies important contacts for interaction. Cell Death Dis, 6, 2015
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4ZIH
| Crystal Structure of core/latch dimer of Bax in complex with BimBH3mini | 分子名称: | Apoptosis regulator BAX, Bcl-2-like protein 11 | 著者 | Robin, A.Y, Krishna Kumar, K, Westphal, D, Wardak, A.Z, Thompson, G.V, Dewson, G, Colman, P.M, Czabotar, P.E. | 登録日 | 2015-04-28 | 公開日 | 2015-07-22 | 最終更新日 | 2023-09-27 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Crystal structure of Bax bound to the BH3 peptide of Bim identifies important contacts for interaction. Cell Death Dis, 6, 2015
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6MCY
| Crystal structure of mouse Bak | 分子名称: | 1,2-ETHANEDIOL, Bcl-2 homologous antagonist/killer, FORMIC ACID | 著者 | Brouwer, J.M, Czabotar, P.E, Colman, P.M. | 登録日 | 2018-09-03 | 公開日 | 2019-09-11 | 最終更新日 | 2023-10-11 | 実験手法 | X-RAY DIFFRACTION (1.748 Å) | 主引用文献 | A small molecule interacts with VDAC2 to block mouse BAK-driven apoptosis. Nat.Chem.Biol., 15, 2019
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6EB6
| Crystal structure of BAX W139A monomer | 分子名称: | Apoptosis regulator BAX, FORMIC ACID | 著者 | Robin, A.Y. | 登録日 | 2018-08-05 | 公開日 | 2019-04-10 | 最終更新日 | 2023-10-11 | 実験手法 | X-RAY DIFFRACTION (2.023 Å) | 主引用文献 | BAX Activation: Mutations Near Its Proposed Non-canonical BH3 Binding Site Reveal Allosteric Changes Controlling Mitochondrial Association. Cell Rep, 27, 2019
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6XA9
| SARS CoV-2 PLpro in complex with ISG15 C-terminal domain propargylamide | 分子名称: | GLYCEROL, ISG15 CTD-propargylamide, Non-structural protein 3, ... | 著者 | Klemm, T, Calleja, D.J, Richardson, L.W, Lechtenberg, B.C, Komander, D. | 登録日 | 2020-06-04 | 公開日 | 2020-06-17 | 最終更新日 | 2024-10-16 | 実験手法 | X-RAY DIFFRACTION (2.9 Å) | 主引用文献 | Mechanism and inhibition of the papain-like protease, PLpro, of SARS-CoV-2. Embo J., 39, 2020
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6XAA
| SARS CoV-2 PLpro in complex with ubiquitin propargylamide | 分子名称: | Non-structural protein 3, Ubiquitin-propargylamide, ZINC ION | 著者 | Klemm, T, Calleja, D.J, Richardson, L.W, Lechtenberg, B.C, Komander, D. | 登録日 | 2020-06-04 | 公開日 | 2020-06-17 | 最終更新日 | 2024-10-23 | 実験手法 | X-RAY DIFFRACTION (2.7 Å) | 主引用文献 | Mechanism and inhibition of the papain-like protease, PLpro, of SARS-CoV-2. Embo J., 39, 2020
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2Y6W
| Structure of a Bcl-w dimer | 分子名称: | BCL-2-LIKE PROTEIN 2, DI(HYDROXYETHYL)ETHER, TRIETHYLENE GLYCOL | 著者 | Lee, E.F, Evangelista, M, Pettikiriarachchi, A, Dogovski, C, Perugini, M.A, Colman, P.M, Fairlie, W.D. | 登録日 | 2011-01-27 | 公開日 | 2011-10-26 | 最終更新日 | 2023-12-20 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Crystal Structure of a Bcl-W Domain-Swapped Dimer: Implications for the Function of Bcl-2 Family Proteins. Structure, 19, 2011
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4U2V
| Bak BH3-in-Groove dimer (GFP) | 分子名称: | (4S)-2-METHYL-2,4-PENTANEDIOL, CACODYLATE ION, Green fluorescent protein,Bcl-2 homologous antagonist/killer | 著者 | Brouwer, J.M, Colman, P.M, Czabotar, P.E. | 登録日 | 2014-07-18 | 公開日 | 2014-09-10 | 最終更新日 | 2024-10-16 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Bak Core and Latch Domains Separate during Activation, and Freed Core Domains Form Symmetric Homodimers. Mol.Cell, 55, 2014
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4U2U
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8UYI
| Structure of ADP-bound and phosphorylated Pediculus humanus (Ph) PINK1 dimer | 分子名称: | ADENOSINE-5'-DIPHOSPHATE, MAGNESIUM ION, Serine/threonine-protein kinase Pink1, ... | 著者 | Gan, Z.Y, Kirk, N.S, Leis, A, Komander, D. | 登録日 | 2023-11-13 | 公開日 | 2024-01-31 | 実験手法 | ELECTRON MICROSCOPY (3.13 Å) | 主引用文献 | Interaction of PINK1 with nucleotides and kinetin. Sci Adv, 10, 2024
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8UYF
| Structure of nucleotide-free Pediculus humanus (Ph) PINK1 dimer | 分子名称: | Serine/threonine-protein kinase Pink1, mitochondrial | 著者 | Gan, Z.Y, Kirk, N.S, Leis, A, Komander, D. | 登録日 | 2023-11-13 | 公開日 | 2024-01-31 | 最終更新日 | 2024-10-09 | 実験手法 | ELECTRON MICROSCOPY (2.75 Å) | 主引用文献 | Interaction of PINK1 with nucleotides and kinetin. Sci Adv, 10, 2024
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8UYH
| Structure of AMP-PNP-bound Pediculus humanus (Ph) PINK1 dimer | 分子名称: | MAGNESIUM ION, PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER, Serine/threonine-protein kinase Pink1, ... | 著者 | Gan, Z.Y, Kirk, N.S, Leis, A, Komander, D. | 登録日 | 2023-11-13 | 公開日 | 2024-01-31 | 最終更新日 | 2024-10-30 | 実験手法 | ELECTRON MICROSCOPY (2.84 Å) | 主引用文献 | Interaction of PINK1 with nucleotides and kinetin. Sci Adv, 10, 2024
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7K02
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5FMK
| Bcl-xL with Bak BH3 complex | 分子名称: | BCL-2 HOMOLOGOUS ANTAGONIST/KILLER, BCL-XL, GLYCEROL | 著者 | Fairlie, W.D, Lee, E.F, Smith, B.J, Czabotar, P.E, Colman, P.M. | 登録日 | 2015-11-06 | 公開日 | 2016-06-01 | 最終更新日 | 2024-01-10 | 実験手法 | X-RAY DIFFRACTION (1.731 Å) | 主引用文献 | Physiological Restraint of Bak by Bcl-Xl is Essential for Cell Survival. Genes Dev., 30, 2016
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5FMI
| Human Bak Q77L | 分子名称: | BCL-2 HOMOLOGOUS ANTAGONIST/KILLER, ZINC ION | 著者 | Fairlie, W.D, Lee, E.F, Smith, B.J. | 登録日 | 2015-11-06 | 公開日 | 2016-06-01 | 最終更新日 | 2024-01-10 | 実験手法 | X-RAY DIFFRACTION (1.491 Å) | 主引用文献 | Physiological Restraint of Bak by Bcl-Xl is Essential for Cell Survival. Genes Dev., 30, 2016
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5FMJ
| Bcl-xL with mouse Bak BH3 Q75L complex | 分子名称: | 1,2-ETHANEDIOL, BAK1 PROTEIN, BCL-2-LIKE PROTEIN 1 | 著者 | Fairlie, W.D, Lee, E.F, Smith, B.J. | 登録日 | 2015-11-06 | 公開日 | 2016-06-01 | 最終更新日 | 2024-01-10 | 実験手法 | X-RAY DIFFRACTION (2.43 Å) | 主引用文献 | Physiological Restraint of Bak by Bcl-Xl is Essential for Cell Survival. Genes Dev., 30, 2016
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