1KD8
| X-RAY STRUCTURE OF THE COILED COIL GCN4 ACID BASE HETERODIMER ACID-d12Ia16V BASE-d12La16L | 分子名称: | GCN4 ACID BASE HETERODIMER ACID-d12Ia16V, GCN4 ACID BASE HETERODIMER BASE-d12La16L | 著者 | Keating, A.E, Malashkevich, V.N, Tidor, B, Kim, P.S. | 登録日 | 2001-11-12 | 公開日 | 2001-11-28 | 最終更新日 | 2024-04-03 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | Side-chain repacking calculations for predicting structures and stabilities of heterodimeric coiled coils. Proc.Natl.Acad.Sci.USA, 98, 2001
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1KD9
| X-RAY STRUCTURE OF THE COILED COIL GCN4 ACID BASE HETERODIMER ACID-d12La16L BASE-d12La16L | 分子名称: | GCN4 ACID BASE HETERODIMER ACID-d12La16L, GCN4 ACID BASE HETERODIMER BASE-d12La16L | 著者 | Keating, A.E, Malashkevich, V.N, Tidor, B, Kim, P.S. | 登録日 | 2001-11-12 | 公開日 | 2001-11-28 | 最終更新日 | 2024-04-03 | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | 主引用文献 | Side-chain repacking calculations for predicting structures and stabilities of heterodimeric coiled coils. Proc.Natl.Acad.Sci.USA, 98, 2001
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1KDD
| X-ray structure of the coiled coil GCN4 ACID BASE HETERODIMER ACID-d12La16I BASE-d12La16L | 分子名称: | GCN4 ACID BASE HETERODIMER ACID-d12La16I, GCN4 ACID BASE HETERODIMER BASE-d12La16L | 著者 | Keating, A.E, Malashkevich, V.N, Tidor, B, Kim, P.S. | 登録日 | 2001-11-12 | 公開日 | 2001-11-28 | 最終更新日 | 2024-04-03 | 実験手法 | X-RAY DIFFRACTION (2.14 Å) | 主引用文献 | Side-chain repacking calculations for predicting structures and stabilities of heterodimeric coiled coils. Proc.Natl.Acad.Sci.USA, 98, 2001
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7LXE
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3MK8
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1XOF
| Heterooligomeric Beta Beta Alpha Miniprotein | 分子名称: | BBAhetT1 | 著者 | Ali, M.H, Taylor, C.M, Grigoryan, G, Allen, K.N, Imperiali, B, Keating, A.E. | 登録日 | 2004-10-06 | 公開日 | 2005-02-01 | 最終更新日 | 2023-11-15 | 実験手法 | X-RAY DIFFRACTION (1.95 Å) | 主引用文献 | Design of a Heterospecific, Tetrameric, 21-Residue Miniprotein with Mixed alpha/beta Structure. Structure, 13, 2005
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6E3J
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6E3I
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8CZH
| Human BAK in complex with the dM2 peptide | 分子名称: | Bcl-2 homologous antagonist/killer, DM2 peptide | 著者 | Aguilar, F, Keating, A.E. | 登録日 | 2022-05-24 | 公開日 | 2023-01-11 | 最終更新日 | 2024-10-09 | 実験手法 | X-RAY DIFFRACTION (1.3 Å) | 主引用文献 | Peptides from human BNIP5 and PXT1 and non-native binders of pro-apoptotic BAK can directly activate or inhibit BAK-mediated membrane permeabilization. Structure, 31, 2023
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8CZF
| Human BAK in complex with the dF2 peptide | 分子名称: | Bcl-2 homologous antagonist/killer, DF2 peptide | 著者 | Aguilar, F, Keating, A.E. | 登録日 | 2022-05-24 | 公開日 | 2023-01-11 | 最終更新日 | 2023-10-25 | 実験手法 | X-RAY DIFFRACTION (1.3 Å) | 主引用文献 | Peptides from human BNIP5 and PXT1 and non-native binders of pro-apoptotic BAK can directly activate or inhibit BAK-mediated membrane permeabilization. Structure, 31, 2023
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8CZG
| Human BAK in complex with the dF3 peptide | 分子名称: | Bcl-2 homologous antagonist/killer, dF3 peptide | 著者 | Aguilar, F, Keating, A.E. | 登録日 | 2022-05-24 | 公開日 | 2023-01-11 | 最終更新日 | 2023-10-25 | 実験手法 | X-RAY DIFFRACTION (1.99 Å) | 主引用文献 | Peptides from human BNIP5 and PXT1 and non-native binders of pro-apoptotic BAK can directly activate or inhibit BAK-mediated membrane permeabilization. Structure, 31, 2023
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6UAB
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6UA3
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6MBB
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6MBE
| Human Mcl-1 in complex with the designed peptide dM7 | 分子名称: | CHLORIDE ION, Induced myeloid leukemia cell differentiation protein Mcl-1, dM7 | 著者 | Jenson, J.M, Keating, A.E. | 登録日 | 2018-08-29 | 公開日 | 2019-03-06 | 最終更新日 | 2023-10-11 | 実験手法 | X-RAY DIFFRACTION (2.25 Å) | 主引用文献 | Tertiary Structural Motif Sequence Statistics Enable Facile Prediction and Design of Peptides that Bind Anti-apoptotic Bfl-1 and Mcl-1. Structure, 27, 2019
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6MBC
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6MBD
| Human Mcl-1 in complex with the designed peptide dM1 | 分子名称: | Induced myeloid leukemia cell differentiation protein Mcl-1, ZINC ION, dM1 | 著者 | Jenson, J.M, Keating, A.E. | 登録日 | 2018-08-29 | 公開日 | 2019-03-06 | 最終更新日 | 2023-10-11 | 実験手法 | X-RAY DIFFRACTION (1.95 Å) | 主引用文献 | Tertiary Structural Motif Sequence Statistics Enable Facile Prediction and Design of Peptides that Bind Anti-apoptotic Bfl-1 and Mcl-1. Structure, 27, 2019
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7LXF
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2PQK
| X-ray crystal structure of human Mcl-1 in complex with Bim BH3 | 分子名称: | Bim BH3 peptide, Induced myeloid leukemia cell differentiation protein Mcl-1, SODIUM ION, ... | 著者 | Bare, E, Grant, R.A, Keating, A.E. | 登録日 | 2007-05-02 | 公開日 | 2007-06-19 | 最終更新日 | 2017-10-18 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Mcl-1-Bim complexes accommodate surprising point mutations via minor structural changes. Protein Sci., 19, 2010
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5UUM
| Human Mcl-1 in complex with a Bfl-1-specific selected peptide | 分子名称: | Bfl-1 specific peptide FS2, Induced myeloid leukemia cell differentiation protein Mcl-1, SULFATE ION, ... | 著者 | Jenson, J.M, Grant, R.A, Keating, A.E. | 登録日 | 2017-02-17 | 公開日 | 2017-06-21 | 最終更新日 | 2024-10-16 | 実験手法 | X-RAY DIFFRACTION (2.346 Å) | 主引用文献 | Epistatic mutations in PUMA BH3 drive an alternate binding mode to potently and selectively inhibit anti-apoptotic Bfl-1. Elife, 6, 2017
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5UUP
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5UUK
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5UUL
| Human Bfl-1 in complex with PUMA BH3 | 分子名称: | Bcl-2-binding component 3, Bcl-2-related protein A1, SULFATE ION | 著者 | Jenson, J.M, Grant, R.A, Keating, A.E. | 登録日 | 2017-02-17 | 公開日 | 2017-06-21 | 最終更新日 | 2023-10-04 | 実験手法 | X-RAY DIFFRACTION (1.33 Å) | 主引用文献 | Epistatic mutations in PUMA BH3 drive an alternate binding mode to potently and selectively inhibit anti-apoptotic Bfl-1. Elife, 6, 2017
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3KJ0
| Mcl-1 in complex with Bim BH3 mutant I2dY | 分子名称: | 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, Bcl-2-like protein 11, Induced myeloid leukemia cell differentiation protein Mcl-1 | 著者 | Fire, E, Grant, R.A, Keating, A.E. | 登録日 | 2009-11-02 | 公開日 | 2010-02-16 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (1.7 Å) | 主引用文献 | Mcl-1-Bim complexes accommodate surprising point mutations via minor structural changes. Protein Sci., 19, 2010
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3KJ1
| Mcl-1 in complex with Bim BH3 mutant I2dA | 分子名称: | ACETATE ION, Bcl-2-like protein 11, CHLORIDE ION, ... | 著者 | Fire, E, Grant, R.A, Keating, A.E. | 登録日 | 2009-11-02 | 公開日 | 2010-02-16 | 最終更新日 | 2023-12-27 | 実験手法 | X-RAY DIFFRACTION (1.945 Å) | 主引用文献 | Mcl-1-Bim complexes accommodate surprising point mutations via minor structural changes. Protein Sci., 19, 2010
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