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PDB: 174 件
5Z90
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BU of 5z90 by Molmil
BRD4 Bromodomain 1 with an inhibitor
分子名称: 1-ethyl-6-pyrrolidin-1-ylsulfonyl-benzo[cd]indol-2-one, Bromodomain-containing protein 4
著者Xiao, S, Chen, S, Chen, H.
登録日2018-02-01
公開日2019-02-06
最終更新日2024-03-27
実験手法X-RAY DIFFRACTION (1.8 Å)
主引用文献BRD4 Bromodomain 1 with an inhibitor
To Be Published
5Z8G
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BU of 5z8g by Molmil
BRD4 Bromodomain 1 with an inhibitor
分子名称: 1-ethyl-6-[(3R)-3-oxidanylpiperidin-1-yl]sulfonyl-benzo[cd]indol-2-one, Bromodomain-containing protein 4, DIMETHYL SULFOXIDE
著者Xiao, S, Chen, S, Chen, H.
登録日2018-01-31
公開日2019-02-06
最終更新日2024-03-27
実験手法X-RAY DIFFRACTION (1.701 Å)
主引用文献BRD4 Bromodomain 1 with an inhibitor
To Be Published
5Z9K
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BU of 5z9k by Molmil
BRD4 Bromodomain 1 with an inhibitor
分子名称: 1-ethyl-6-[(2R)-2-(hydroxymethyl)pyrrolidin-1-yl]sulfonyl-benzo[cd]indol-2-one, Bromodomain-containing protein 4
著者Xiao, S, Chen, S, Chen, H.
登録日2018-02-03
公開日2019-02-06
最終更新日2024-03-27
実験手法X-RAY DIFFRACTION (1.89 Å)
主引用文献BRD4 Bromodomain 1 with an inhibitor
To Be Published
5Z8R
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BU of 5z8r by Molmil
BRD4 Bromodomain 1 with an inhibitor
分子名称: 1-ethyl-6-[(3S)-3-oxidanylpiperidin-1-yl]sulfonyl-benzo[cd]indol-2-one, Bromodomain-containing protein 4
著者Xiao, S, Chen, S, Chen, H.
登録日2018-02-01
公開日2019-02-06
最終更新日2024-03-27
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献BRD4 Bromodomain 1 with an inhibitor
To Be Published
5Z8Z
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BU of 5z8z by Molmil
BRD4 Bromodomain 1 with an inhibitor
分子名称: 6-[(3S)-3-azanylpiperidin-1-yl]sulfonyl-1-ethyl-benzo[cd]indol-2-one, Bromodomain-containing protein 4
著者Xiao, S, Chen, S, Chen, H.
登録日2018-02-01
公開日2019-02-06
最終更新日2024-03-27
実験手法X-RAY DIFFRACTION (1.8 Å)
主引用文献BRD4 Bromodomain 1 with an inhibitor
To Be Published
6KEE
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BU of 6kee by Molmil
Crystal structure of BRD4 Bromodomain1 with an inhibitor
分子名称: 6-[2-[2,4-bis(fluoranyl)phenoxy]-5-(methylsulfonylmethyl)pyridin-3-yl]-8-methyl-2H-pyrrolo[1,2-a]pyrazin-1-one, Bromodomain-containing protein 4
著者Xiao, S, Li, Z, Chen, S, Zhou, B, Luo, C.
登録日2019-07-04
公開日2020-07-08
最終更新日2023-11-22
実験手法X-RAY DIFFRACTION (2.12154651 Å)
主引用文献Crystal structure of BRD4 Bromodomain1 with an inhibitor
To be published
6KEG
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BU of 6keg by Molmil
BRD4 Bromodomain1 with an inhibitor
分子名称: 6-[2-[2,4-bis(fluoranyl)phenoxy]-5-(ethylsulfonylmethyl)pyridin-3-yl]-8-methyl-4H-pyrrolo[1,2-a]pyrazin-1-one, Bromodomain-containing protein 4
著者Xiao, S, Li, Z, Chen, S, Zhou, B, Luo, C.
登録日2019-07-04
公開日2020-07-08
最終更新日2024-03-27
実験手法X-RAY DIFFRACTION (2.232 Å)
主引用文献BRD4 Bromodomain1 with an inhibitor
To Be Published
6KEF
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BU of 6kef by Molmil
BRD4 Bromodomain1 with an inhibitor
分子名称: Bromodomain-containing protein 4, N-[3-(8-methyl-1-oxidanylidene-2H-pyrrolo[1,2-a]pyrazin-6-yl)-4-phenoxy-phenyl]methanesulfonamide
著者Xiao, S, Li, Z, Chen, S, Zhou, B, Luo, C.
登録日2019-07-04
公開日2020-07-08
最終更新日2024-03-27
実験手法X-RAY DIFFRACTION (2.44467545 Å)
主引用文献BRD4 Bromodomain1 with an inhibitor
To Be Published
6KED
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BU of 6ked by Molmil
BRD4 Bromodomain1 with an inhibitor
分子名称: 6-[2-[2,4-bis(fluoranyl)phenoxy]-5-(methylsulfonylmethyl)pyridin-3-yl]-8-methyl-2H-pyrrolo[1,2-d][1,2,4]triazin-1-one, Bromodomain-containing protein 4
著者Xiao, S, Li, Z, Chen, S, Zhou, B, Luo, C.
登録日2019-07-04
公開日2020-07-08
最終更新日2024-03-27
実験手法X-RAY DIFFRACTION (2.548447 Å)
主引用文献BRD4 Bromodomain1 with an inhibitor
To Be Published
2N9D
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BU of 2n9d by Molmil
Structure analysis of the Tom1 GAT domain reveals distinct ligand-specific conformational states
分子名称: Target of Myb protein 1
著者Xiao, S, Jeffrey, E.F, Geoffrey, A.S, Capelluto, D.G.S.
登録日2015-11-15
公開日2016-09-21
最終更新日2024-05-01
実験手法SOLUTION NMR
主引用文献Structure of the GAT domain of the endosomal adapter protein Tom1.
Data Brief, 7, 2016
2N2N
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BU of 2n2n by Molmil
Tom1 negatively modulates binding of Tollip to phosphatidylinositol 3-phosphate via a coupled folding and binding mechanism
分子名称: Target of Myb protein 1
著者Xiao, S, Armstrong, G, Capelluto, D.
登録日2015-05-11
公開日2015-09-16
最終更新日2024-05-15
実験手法SOLUTION NMR
主引用文献Tom1 Modulates Binding of Tollip to Phosphatidylinositol 3-Phosphate via a Coupled Folding and Binding Mechanism.
Structure, 23, 2015
2N31
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Tom1 negatively modulates binding of Tollip to phosphatidylinositol 3-phosphate via a coupled folding and binding mechanism
分子名称: Toll interacting protein variant
著者Xiao, S, Armstrong, G, Capelluto, D.
登録日2015-05-19
公開日2015-09-16
最終更新日2024-05-15
実験手法SOLUTION NMR
主引用文献Tom1 Modulates Binding of Tollip to Phosphatidylinositol 3-Phosphate via a Coupled Folding and Binding Mechanism.
Structure, 23, 2015
3BG5
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BU of 3bg5 by Molmil
Crystal Structure of Staphylococcus Aureus Pyruvate Carboxylase
分子名称: 5-(HEXAHYDRO-2-OXO-1H-THIENO[3,4-D]IMIDAZOL-6-YL)PENTANAL, ADENOSINE-5'-TRIPHOSPHATE, MANGANESE (II) ION, ...
著者Xiang, S, Tong, L.
登録日2007-11-26
公開日2008-02-26
最終更新日2023-11-15
実験手法X-RAY DIFFRACTION (2.8 Å)
主引用文献Crystal structures of human and Staphylococcus aureus pyruvate carboxylase and molecular insights into the carboxyltransfer reaction.
Nat.Struct.Mol.Biol., 15, 2008
3BG3
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BU of 3bg3 by Molmil
Crystal Structure of Human Pyruvate Carboxylase (missing the biotin carboxylase domain at the N-terminus)
分子名称: 5-(HEXAHYDRO-2-OXO-1H-THIENO[3,4-D]IMIDAZOL-6-YL)PENTANAL, MANGANESE (II) ION, PYRUVIC ACID, ...
著者Xiang, S, Tong, L.
登録日2007-11-26
公開日2008-02-26
最終更新日2023-11-15
実験手法X-RAY DIFFRACTION (2.8 Å)
主引用文献Crystal structures of human and Staphylococcus aureus pyruvate carboxylase and molecular insights into the carboxyltransfer reaction.
Nat.Struct.Mol.Biol., 15, 2008
2DFK
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BU of 2dfk by Molmil
Crystal structure of the CDC42-Collybistin II complex
分子名称: GLYCEROL, SULFATE ION, cell division cycle 42 isoform 1, ...
著者Xiang, S, Kim, E.Y, Connelly, J.J, Nassar, N, Kirsch, J, Winking, J, Schwarz, G, Schindelin, H.
登録日2006-03-02
公開日2006-05-02
最終更新日2023-10-25
実験手法X-RAY DIFFRACTION (2.15 Å)
主引用文献The Crystal Structure of Cdc42 in Complex with Collybistin II, a Gephyrin-interacting Guanine Nucleotide Exchange Factor.
J.Mol.Biol., 359, 2006
3BG9
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BU of 3bg9 by Molmil
Crystal Structure of Human Pyruvate Carboxylase (missing the biotin carboxylase domain at the N-terminus) F1077A Mutant
分子名称: MANGANESE (II) ION, Pyruvate carboxylase, mitochondrial
著者Xiang, S, Tong, L.
登録日2007-11-26
公開日2008-02-26
最終更新日2024-02-21
実験手法X-RAY DIFFRACTION (3 Å)
主引用文献Crystal structures of human and Staphylococcus aureus pyruvate carboxylase and molecular insights into the carboxyltransfer reaction.
Nat.Struct.Mol.Biol., 15, 2008
3K8X
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BU of 3k8x by Molmil
Crystal structure of the carboxyltransferase domain of acetyl-coenzyme A carboxylase in complex with tepraloxydim
分子名称: (5S)-2-[(1E)-N-{[(2E)-3-chloroprop-2-en-1-yl]oxy}propanimidoyl]-3-hydroxy-5-(tetrahydro-2H-pyran-4-yl)cyclohex-2-en-1-one, Acetyl-CoA carboxylase
著者Xiang, S, Callaghan, M.M, Watson, K.G, Tong, L.
登録日2009-10-15
公開日2009-12-01
最終更新日2024-02-21
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献A different mechanism for the inhibition of the carboxyltransferase domain of acetyl-coenzyme A carboxylase by tepraloxydim.
Proc.Natl.Acad.Sci.USA, 106, 2009
1AF2
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BU of 1af2 by Molmil
CRYSTAL STRUCTURE OF CYTIDINE DEAMINASE COMPLEXED WITH URIDINE
分子名称: CYTIDINE DEAMINASE, URIDINE-5'-MONOPHOSPHATE, ZINC ION
著者Xiang, S, Carter, C.W.
登録日1997-03-20
公開日1997-07-07
最終更新日2024-05-22
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献The structure of the cytidine deaminase-product complex provides evidence for efficient proton transfer and ground-state destabilization.
Biochemistry, 36, 1997
1CTU
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BU of 1ctu by Molmil
TRANSITION-STATE SELECTIVITY FOR A SINGLE OH GROUP DURING CATALYSIS BY CYTIDINE DEAMINASE
分子名称: 4-HYDROXY-3,4-DIHYDRO-ZEBULARINE, CYTIDINE DEAMINASE, ZINC ION
著者Xiang, S, Short, S.A, Wolfenden, R, Carter, C.W.
登録日1995-02-11
公開日1995-05-08
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Transition-state selectivity for a single hydroxyl group during catalysis by cytidine deaminase.
Biochemistry, 34, 1995
1CTT
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BU of 1ctt by Molmil
TRANSITION-STATE SELECTIVITY FOR A SINGLE OH GROUP DURING CATALYSIS BY CYTIDINE DEAMINASE
分子名称: 3,4-DIHYDRO-1H-PYRIMIDIN-2-ONE NUCLEOSIDE, CYTIDINE DEAMINASE, ZINC ION
著者Xiang, S, Short, S.A, Wolfenden, R, Carter, C.W.
登録日1995-02-11
公開日1995-05-08
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献Transition-state selectivity for a single hydroxyl group during catalysis by cytidine deaminase.
Biochemistry, 34, 1995
1ALN
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BU of 1aln by Molmil
CRYSTAL STRUCTURE OF CYTIDINE DEAMINASE COMPLEXED WITH 3-DEAZACYTIDINE
分子名称: 3-DEAZACYTIDINE, CYTIDINE DEAMINASE, ZINC ION
著者Xiang, S, Carter, C.W.
登録日1997-06-02
公開日1997-09-17
最終更新日2024-05-22
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Cytidine deaminase complexed to 3-deazacytidine: a "valence buffer" in zinc enzyme catalysis.
Biochemistry, 35, 1996
3FQG
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BU of 3fqg by Molmil
Crystal Structure of the S. pombe Rai1
分子名称: MAGNESIUM ION, Protein din1
著者Xiang, S, Tong, L.
登録日2009-01-07
公開日2009-02-03
最終更新日2024-02-21
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Structure and function of the 5'-->3' exoribonuclease Rat1 and its activating partner Rai1.
Nature, 458, 2009
3FQI
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Crystal Structure of the Mouse Dom3Z
分子名称: 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID, MAGNESIUM ION, Protein Dom3Z
著者Xiang, S, Tong, L.
登録日2009-01-07
公開日2009-02-03
最終更新日2024-02-21
実験手法X-RAY DIFFRACTION (2.013 Å)
主引用文献Structure and function of the 5'-->3' exoribonuclease Rat1 and its activating partner Rai1.
Nature, 458, 2009
3FQD
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Crystal Structure of the S. pombe Rat1-Rai1 Complex
分子名称: 5'-3' exoribonuclease 2, GLYCEROL, MAGNESIUM ION, ...
著者Xiang, S, Tong, L.
登録日2009-01-07
公開日2009-02-03
最終更新日2017-11-01
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献Structure and function of the 5'-->3' exoribonuclease Rat1 and its activating partner Rai1.
Nature, 458, 2009
2LSW
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Structure, sulfatide-binding properties, and inhibition of platelet aggregation by a Disabled-2-derived peptide
分子名称: Disabled homolog 2
著者Xiao, S.
登録日2012-05-08
公開日2012-09-19
最終更新日2024-05-15
実験手法SOLUTION NMR
主引用文献Structure, Sulfatide Binding Properties, and Inhibition of Platelet Aggregation by a Disabled-2 Protein-derived Peptide.
J.Biol.Chem., 287, 2012

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