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PDB: 174 件

1U5G
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Crystal Structure of the PH Domain of SKAP-Hom
分子名称: Src-associated adaptor protein
著者Tang, Y, Swanson, K, Neel, B.G, Eck, M.J.
登録日2004-07-27
公開日2005-07-26
最終更新日2023-08-23
実験手法X-RAY DIFFRACTION (2.1 Å)
主引用文献The Skap-hom dimerization and PH domains comprise a 3'-phosphoinositide-gated molecular switch.
Mol.Cell, 32, 2008
4YYG
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Crystal structure of BRD9 Bromodomain bound to a butyryllysine peptide
分子名称: Bromodomain-containing protein 9, Histone H4
著者Tang, Y, Bellon, S, Cochran, A.G, Poy, F.
登録日2015-03-23
公開日2015-09-16
最終更新日2023-09-27
実験手法X-RAY DIFFRACTION (2.1 Å)
主引用文献A Subset of Human Bromodomains Recognizes Butyryllysine and Crotonyllysine Histone Peptide Modifications.
Structure, 23, 2015
4YYJ
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Crystal structure of BRD9 Bromodomain bound to a butyryllysine peptide
分子名称: Bromodomain-containing protein 9, Histone H4
著者Tang, Y, Bellon, S, Cochran, A.G, Poy, F.
登録日2015-03-23
公開日2015-09-16
最終更新日2023-09-27
実験手法X-RAY DIFFRACTION (1.85 Å)
主引用文献A Subset of Human Bromodomains Recognizes Butyryllysine and Crotonyllysine Histone Peptide Modifications.
Structure, 23, 2015
3Q35
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Structure of the Rtt109-AcCoA/Vps75 complex and implications for chaperone-mediated histone acetylation
分子名称: 1,2-ETHANEDIOL, ACETYL COENZYME *A, Histone acetyltransferase, ...
著者Tang, Y, Yuan, H, Meeth, K, Marmorstein, R.
登録日2010-12-21
公開日2011-02-02
最終更新日2023-12-06
実験手法X-RAY DIFFRACTION (3.3 Å)
主引用文献Structure of the Rtt109-AcCoA/Vps75 Complex and Implications for Chaperone-Mediated Histone Acetylation.
Structure, 19, 2011
3Q33
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Structure of the Rtt109-AcCoA/Vps75 Complex and Implications for Chaperone-Mediated Histone Acetylation
分子名称: 1,2-ETHANEDIOL, ACETYL COENZYME *A, HISTONE H3, ...
著者Tang, Y, Yuan, H, Meeth, K, Marmorstein, R.
登録日2010-12-21
公開日2011-02-02
最終更新日2023-12-06
実験手法X-RAY DIFFRACTION (2.8 Å)
主引用文献Structure of the Rtt109-AcCoA/Vps75 Complex and Implications for Chaperone-Mediated Histone Acetylation.
Structure, 19, 2011
5KPH
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Solution NMR Structure of Denovo Beta Sheet Design Protein, Northeast Structural Genomics Consortium (NESG) Target OR485
分子名称: De novo Beta Sheet Design Protein OR485
著者Tang, Y, Liu, G, Montelione, G.T, Northeast Structural Genomics Consortium (NESG)
登録日2016-07-04
公開日2016-09-28
最終更新日2024-05-15
実験手法SOLUTION NMR
主引用文献Principles for designing proteins with cavities formed by curved beta sheets.
Science, 355, 2017
5KPE
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Solution NMR Structure of Denovo Beta Sheet Design Protein, Northeast Structural Genomics Consortium (NESG) Target OR664
分子名称: De novo Beta Sheet Design Protein OR664
著者Tang, Y, Liu, G, Baker, D, Montelione, G.T, Northeast Structural Genomics Consortium (NESG)
登録日2016-07-03
公開日2016-09-21
最終更新日2024-05-15
実験手法SOLUTION NMR
主引用文献Principles for designing proteins with cavities formed by curved beta sheets.
Science, 355, 2017
5I1Q
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Second bromodomain of TAF1 bound to a pyrrolopyridone compound
分子名称: 3-[6-(but-3-en-1-yl)-7-oxo-6,7-dihydro-1H-pyrrolo[2,3-c]pyridin-4-yl]-N,N-dimethylbenzamide, Transcription initiation factor TFIID subunit 1
著者Tang, Y, Poy, F, Bellon, S.F.
登録日2016-01-09
公開日2016-06-08
最終更新日2023-09-27
実験手法X-RAY DIFFRACTION (1.5 Å)
主引用文献Diving into the Water: Inducible Binding Conformations for BRD4, TAF1(2), BRD9, and CECR2 Bromodomains.
J.Med.Chem., 59, 2016
5I29
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TAF1(2) bound to a pyrrolopyridone compound
分子名称: CALCIUM ION, N,N-dimethyl-3-(6-methyl-7-oxo-6,7-dihydro-1H-pyrrolo[2,3-c]pyridin-4-yl)benzamide, Transcription initiation factor TFIID subunit 1
著者Tang, Y, Poy, F, Bellon, S.F.
登録日2016-02-08
公開日2016-06-08
最終更新日2023-09-27
実験手法X-RAY DIFFRACTION (1.21 Å)
主引用文献Diving into the Water: Inducible Binding Conformations for BRD4, TAF1(2), BRD9, and CECR2 Bromodomains.
J.Med.Chem., 59, 2016
2HG4
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BU of 2hg4 by Molmil
Structure of the ketosynthase-acyltransferase didomain of module 5 from DEBS.
分子名称: 6-Deoxyerythronolide B Synthase, ACETATE ION, CHLORIDE ION, ...
著者Tang, Y, Kim, C.Y, Mathews, I.I, Cane, D.E, Khosla, C.
登録日2006-06-26
公開日2006-07-11
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (2.73 Å)
主引用文献The 2.7-A crystal structure of a 194-kDa homodimeric fragment of the 6-deoxyerythronolide B synthase.
Proc.Natl.Acad.Sci.Usa, 103, 2006
3DM7
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BU of 3dm7 by Molmil
Crystal Structure of the Vps75 Histone Chaperone
分子名称: Vacuolar protein sorting-associated protein 75
著者Tang, Y, Marmorstein, R.
登録日2008-06-30
公開日2008-09-09
最終更新日2021-10-20
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Structure of Vps75 and implications for histone chaperone function.
Proc.Natl.Acad.Sci.Usa, 105, 2008
8T8Q
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Identification of GDC-1971 (RLY-1971), a SHP2 inhibitor designed for the treatment of solid tumors
分子名称: 1-[(3P)-3-(3-chloro-2-fluorophenyl)-1H-pyrazolo[3,4-b]pyrazin-6-yl]-4-methylpiperidin-4-amine, Tyrosine-protein phosphatase non-receptor type 11
著者Tang, Y, Nguyen, V, Wilbur, J.D.
登録日2023-06-23
公開日2023-10-11
最終更新日2023-10-25
実験手法X-RAY DIFFRACTION (2.27 Å)
主引用文献Identification of GDC-1971 (RLY-1971), a SHP2 Inhibitor Designed for the Treatment of Solid Tumors.
J.Med.Chem., 66, 2023
8T7Q
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Identification of GDC-1971 (RLY-1971), a SHP2 inhibitor designed for the treatment of solid tumors
分子名称: 1-{3-[(2-chlorophenyl)sulfanyl]-1H-pyrazolo[3,4-b]pyrazin-6-yl}-4-methylpiperidin-4-amine, Tyrosine-protein phosphatase non-receptor type 11
著者Tang, Y, Nguyen, V, Wilbur, J.D.
登録日2023-06-21
公開日2023-10-11
最終更新日2023-10-25
実験手法X-RAY DIFFRACTION (2.1 Å)
主引用文献Identification of GDC-1971 (RLY-1971), a SHP2 Inhibitor Designed for the Treatment of Solid Tumors.
J.Med.Chem., 66, 2023
8T6D
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Identification of GDC-1971 (RLY-1971), a SHP2 inhibitor designed for the treatment of solid tumors
分子名称: (3R)-1'-[3-(3,4-dihydro-1,5-naphthyridin-1(2H)-yl)-1H-pyrazolo[3,4-b]pyrazin-6-yl]-3H-spiro[[1]benzofuran-2,4'-piperidin]-3-amine, SULFATE ION, Tyrosine-protein phosphatase non-receptor type 11
著者Tang, Y, Nguyen, V, Wilbur, J.D.
登録日2023-06-15
公開日2023-10-11
最終更新日2023-10-25
実験手法X-RAY DIFFRACTION (2.4 Å)
主引用文献Identification of GDC-1971 (RLY-1971), a SHP2 Inhibitor Designed for the Treatment of Solid Tumors.
J.Med.Chem., 66, 2023
8T6G
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BU of 8t6g by Molmil
Identification of GDC-1971 (RLY-1971), a SHP2 inhibitor designed for the treatment of solid tumors
分子名称: (1S)-1-{6-[(1S)-1-amino-1,3-dihydrospiro[indene-2,4'-piperidin]-1'-yl]-3-(3,4-dihydro-1,5-naphthyridin-1(2H)-yl)-1H-pyrazolo[3,4-b]pyrazin-5-yl}ethan-1-ol, SULFATE ION, Tyrosine-protein phosphatase non-receptor type 11
著者Tang, Y, Nugyen, V, Wilbur, J.D.
登録日2023-06-15
公開日2023-10-11
最終更新日2023-10-25
実験手法X-RAY DIFFRACTION (1.84 Å)
主引用文献Identification of GDC-1971 (RLY-1971), a SHP2 Inhibitor Designed for the Treatment of Solid Tumors.
J.Med.Chem., 66, 2023
4YY6
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BU of 4yy6 by Molmil
Crystal structure of BRD9 Bromodomain bound to a butyryllysine peptide
分子名称: Bromodomain-containing protein 9, Histone H4
著者Tang, Y, Bellon, S, Cochran, A.G, Poy, F.
登録日2015-03-23
公開日2015-09-16
最終更新日2023-09-27
実験手法X-RAY DIFFRACTION (1.45 Å)
主引用文献A Subset of Human Bromodomains Recognizes Butyryllysine and Crotonyllysine Histone Peptide Modifications.
Structure, 23, 2015
4YYD
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BU of 4yyd by Molmil
Crystal structure of BRD9 Bromodomain bound to a crotonyllysine peptide
分子名称: Bromodomain-containing protein 9, Histone H4
著者Tang, Y, Bellon, S, Cochran, A.G, Poy, F.
登録日2015-03-23
公開日2015-09-16
最終更新日2023-11-15
実験手法X-RAY DIFFRACTION (1.52 Å)
主引用文献A Subset of Human Bromodomains Recognizes Butyryllysine and Crotonyllysine Histone Peptide Modifications.
Structure, 23, 2015
4YYH
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BU of 4yyh by Molmil
Crystal structure of BRD9 Bromodomain bound to a crotonyllysine peptide
分子名称: Bromodomain-containing protein 9, Histone H4
著者Tang, Y, Bellon, S, Cochran, A.G, Poy, F.
登録日2015-03-23
公開日2015-09-16
最終更新日2023-11-15
実験手法X-RAY DIFFRACTION (1.74 Å)
主引用文献A Subset of Human Bromodomains Recognizes Butyryllysine and Crotonyllysine Histone Peptide Modifications.
Structure, 23, 2015
4YYN
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BU of 4yyn by Molmil
Crystal structure of TAF1 BD2 Bromodomain bound to a crotonyllysine peptide
分子名称: Histone H4, Transcription initiation factor TFIID subunit 1
著者Tang, Y, Bellon, S, Cochran, A.G, Poy, F.
登録日2015-03-24
公開日2015-09-16
最終更新日2023-11-15
実験手法X-RAY DIFFRACTION (1.85 Å)
主引用文献A Subset of Human Bromodomains Recognizes Butyryllysine and Crotonyllysine Histone Peptide Modifications.
Structure, 23, 2015
4YYK
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BU of 4yyk by Molmil
Crystal structure of BRD9 Bromodomain bound to a crotonyllysine peptide
分子名称: Bromodomain-containing protein 9, Histone H4
著者Tang, Y, Bellon, S, Cochran, A.G, Poy, F.
登録日2015-03-24
公開日2015-09-16
最終更新日2023-11-15
実験手法X-RAY DIFFRACTION (1.79 Å)
主引用文献A Subset of Human Bromodomains Recognizes Butyryllysine and Crotonyllysine Histone Peptide Modifications.
Structure, 23, 2015
4YY4
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Crystal structure of BRD9 Bromodomain bound to DMSO
分子名称: Bromodomain-containing protein 9, DIMETHYL SULFOXIDE
著者Tang, Y, Bellon, S, Cochran, A.G, Poy, F.
登録日2015-03-23
公開日2015-09-16
最終更新日2023-09-27
実験手法X-RAY DIFFRACTION (1.47 Å)
主引用文献A Subset of Human Bromodomains Recognizes Butyryllysine and Crotonyllysine Histone Peptide Modifications.
Structure, 23, 2015
4YYM
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BU of 4yym by Molmil
Crystal structure of TAF1 BD2 Bromodomain bound to a butyryllysine peptide
分子名称: CALCIUM ION, Histone H4, Transcription initiation factor TFIID subunit 1
著者Tang, Y, Bellon, S, Cochran, A.G, Poy, F.
登録日2015-03-24
公開日2015-09-16
最終更新日2023-09-27
実験手法X-RAY DIFFRACTION (1.5 Å)
主引用文献A Subset of Human Bromodomains Recognizes Butyryllysine and Crotonyllysine Histone Peptide Modifications.
Structure, 23, 2015
4YYI
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BU of 4yyi by Molmil
Crystal structure of BRD9 Bromodomain bound to an acetylated peptide
分子名称: Bromodomain-containing protein 9, Histone H4
著者Tang, Y, Bellon, S, Cochran, A.G, Poy, F.
登録日2015-03-23
公開日2015-09-16
最終更新日2023-11-15
実験手法X-RAY DIFFRACTION (1.5 Å)
主引用文献A Subset of Human Bromodomains Recognizes Butyryllysine and Crotonyllysine Histone Peptide Modifications.
Structure, 23, 2015
7TAB
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BU of 7tab by Molmil
G-925 bound to the SMARCA4 (BRG1) Bromodomain
分子名称: 2-(6-amino-5-phenylpyridazin-3-yl)phenol, Isoform 4 of Transcription activator BRG1
著者Tang, Y, Poy, F, Taylor, A.M, Cochran, A.G, Bellon, S.F.
登録日2021-12-20
公開日2022-08-17
最終更新日2023-10-18
実験手法X-RAY DIFFRACTION (1.16 Å)
主引用文献GNE-064: A Potent, Selective, and Orally Bioavailable Chemical Probe for the Bromodomains of SMARCA2 and SMARCA4 and the Fifth Bromodomain of PBRM1.
J.Med.Chem., 65, 2022
7TD9
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G-059 bound to the SMARCA4 (BRG1) Bromodomain
分子名称: 4-phenyl-5H-pyridazino[4,3-b]indol-3-amine, Isoform 4 of Transcription activator BRG1
著者Tang, Y, Poy, F, Taylor, A.M, Cochran, A.G, Bellon, S.F.
登録日2021-12-30
公開日2022-08-17
最終更新日2023-10-18
実験手法X-RAY DIFFRACTION (1.61 Å)
主引用文献GNE-064: A Potent, Selective, and Orally Bioavailable Chemical Probe for the Bromodomains of SMARCA2 and SMARCA4 and the Fifth Bromodomain of PBRM1.
J.Med.Chem., 65, 2022

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