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PDB: 98 件

6D8X
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PPAR gamma LBD complexed with the agonist GW1929
分子名称: (2~{S})-3-[4-[2-[methyl(pyridin-2-yl)amino]ethoxy]phenyl]-2-[[2-(phenylcarbonyl)phenyl]amino]propanoic acid, CITRATE ANION, GLYCEROL, ...
著者Mou, T.C, Chrisman, I.M, Hughes, T.S, Sprang, S.R.
登録日2018-04-27
公開日2019-05-01
最終更新日2023-10-04
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献PPAR gamma LBD complexed with the agonist GW1929
To Be Published
6MFA
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Fragment of human fibronectin containing the 4th-7th type III domains
分子名称: Fibronectin
著者Loa, S, Mou, T.C, Sprang, S.R, Briknarova, K.
登録日2018-09-10
公開日2019-09-18
最終更新日2023-10-11
実験手法X-RAY DIFFRACTION (1.754 Å)
主引用文献Fragment of human fibronectin containing the 4th-7th type III domains, crystal form I
To Be Published
5T7H
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Crystal structure of dimeric yeast iso-1-cytochrome C with CYMAL6
分子名称: 6-cyclohexylhexan-1-ol, Cytochrome c iso-1, HEME C, ...
著者Mcclelland, L, Mou, T.C, Sprang, S.R, Bowler, B.E.
登録日2016-09-05
公開日2017-03-22
最終更新日2023-10-04
実験手法X-RAY DIFFRACTION (2.003 Å)
主引用文献Cytochrome c Can Form a Well-Defined Binding Pocket for Hydrocarbons.
J. Am. Chem. Soc., 138, 2016
6MSV
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Structure of the 6th type III domain from human fibronectin
分子名称: Fibronectin, GLYCEROL
著者Loa, S, Mou, T.C, Sprang, S.R, Briknarova, K.
登録日2018-10-18
公開日2019-10-23
最終更新日2023-10-11
実験手法X-RAY DIFFRACTION (2.4 Å)
主引用文献Structure of the 6th type III domain from human fibronectin
To Be Published
6DCU
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Crystal structure of PPAR gamma co-crystallized with nTZDpa
分子名称: 5-CHLORO-1-(4-CHLOROBENZYL)-3-(PHENYLTHIO)-1H-INDOLE-2-CARBOXYLIC ACID, Peroxisome proliferator-activated receptor gamma
著者Mou, T.C, Chrisman, I.M, Hughes, T.S, Sprang, S.R.
登録日2018-05-08
公開日2019-05-15
最終更新日2023-10-11
実験手法X-RAY DIFFRACTION (2.95 Å)
主引用文献Crystal structure of PPAR gamma in complex with NMP422
To Be Published
6DBH
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Crystal structure of PPAR gamma in complex with NMP422
分子名称: 4-{2-[(2,3-dioxo-1-pentyl-2,3-dihydro-1H-indol-5-yl)sulfanyl]ethyl}benzoic acid, CHLORIDE ION, Peroxisome proliferator-activated receptor gamma
著者Mou, T.C, Chrisman, I.M, Hughes, T.S, Sprang, S.R.
登録日2018-05-03
公開日2019-05-08
最終更新日2023-10-04
実験手法X-RAY DIFFRACTION (2.597 Å)
主引用文献Crystal structure of PPAR gamma in complex with NMP422
To Be Published
6MM1
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Structure of the cysteine-rich region from human EHMT2
分子名称: Histone-lysine N-methyltransferase EHMT2, ZINC ION
著者Kerchner, K.M, Mou, T.C, Sprang, S.R, Briknarova, K.
登録日2018-09-28
公開日2019-10-02
最終更新日2024-05-22
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献The structure of the cysteine-rich region from human histone-lysine N-methyltransferase EHMT2 (G9a).
J Struct Biol X, 5, 2021
6XAZ
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Structure of the PR domain from human PRDM5
分子名称: DI(HYDROXYETHYL)ETHER, PR domain zinc finger protein 5
著者Mou, T.C, Kerchner, K.M, Sprang, S.R, Briknarova, K.
登録日2020-06-05
公開日2021-06-09
最終更新日2023-10-18
実験手法X-RAY DIFFRACTION (1.7 Å)
主引用文献Structure of the PR domain from human PRDM5
To Be Published
6XAX
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Structure of a fragment of human fibronectin containing the 11th type III domain, extra domain A, and the 12th type III domain
分子名称: Fibronectin, GLYCEROL
著者Mou, T.C, Nepomuceno, P.A, Sprang, S.R, Briknarova, K.
登録日2020-06-04
公開日2021-06-09
最終更新日2023-10-18
実験手法X-RAY DIFFRACTION (2.4 Å)
主引用文献Fragment of human fibronectin containing the 11th type III domain, extra domain A, and 12th type III domain
To Be Published
6XAY
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Structure of a fragment of human fibronectin containing the 10th, 11th and 12th type III domains
分子名称: Fibronectin, GLYCEROL
著者Mou, T.C, Nepomuceno, P.A, Sprang, S.R, Briknarova, K.
登録日2020-06-05
公開日2021-06-09
最終更新日2023-10-18
実験手法X-RAY DIFFRACTION (2.48 Å)
主引用文献Fragment of human fibronectin containing the 10th, 11th and 12th type III domains
To Be Published
1TNF
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BU of 1tnf by Molmil
THE STRUCTURE OF TUMOR NECROSIS FACTOR-ALPHA AT 2.6 ANGSTROMS RESOLUTION. IMPLICATIONS FOR RECEPTOR BINDING
分子名称: TUMOR NECROSIS FACTOR-ALPHA
著者Eck, M.J, Sprang, S.R.
登録日1989-08-25
公開日1990-01-15
最終更新日2024-06-05
実験手法X-RAY DIFFRACTION (2.6 Å)
主引用文献The structure of tumor necrosis factor-alpha at 2.6 A resolution. Implications for receptor binding.
J.Biol.Chem., 264, 1989
6NMG
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Crystal Structure of Rat Ric-8A G alpha binding domain
分子名称: Resistance to inhibitors of cholinesterase 8 homolog A (C. elegans), SULFATE ION
著者Zeng, B, Mou, T.C, Sprang, S.R.
登録日2019-01-10
公開日2019-06-26
最終更新日2024-03-13
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献Structure, Function, and Dynamics of the G alpha Binding Domain of Ric-8A.
Structure, 27, 2019
6W2H
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Crystal Structure of the Internal UBA Domain of HHR23A
分子名称: SULFATE ION, UV excision repair protein RAD23 homolog A
著者Bowler, B.E, Zeng, B, Becht, D.C, Rothfuss, M, Sprang, S.R, Mou, T.-C.
登録日2020-03-05
公開日2021-03-10
最終更新日2024-04-03
実験手法X-RAY DIFFRACTION (1.6 Å)
主引用文献Residual Structure in the Denatured State of the Fast-Folding UBA(1) Domain from the Human DNA Excision Repair Protein HHR23A.
Biochemistry, 61, 2022
6NMJ
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Crystal Structure of Rat Ric-8A G alpha binding domain, "Paratone-N Immersed"
分子名称: Resistance to inhibitors of cholinesterase 8 homolog A (C. elegans)
著者Zeng, B, Mou, T.C, Sprang, S.R.
登録日2019-01-11
公開日2019-06-26
最終更新日2023-10-11
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Structure, Function, and Dynamics of the G alpha Binding Domain of Ric-8A.
Structure, 27, 2019
6OVD
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Crystal structure of GluN1/GluN2A NMDA receptor agonist binding domains with glycine and antagonist, 3-ethylphenyl-ACEPC
分子名称: (3S,5S)-5-[(2R)-2-amino-2-carboxyethyl]-1-(3-ethylphenyl)pyrazolidine-3-carboxylic acid, GLYCINE, Glutamate receptor ionotropic, ...
著者Syrenne, J.T, Mou, T.C, Tamborini, L, Pinto, A, Sprang, S.R, Hansen, K.B.
登録日2019-05-07
公開日2020-05-13
最終更新日2023-10-11
実験手法X-RAY DIFFRACTION (2.102 Å)
主引用文献Crystal structure of GluN1/GluN2A NMDA receptor agonist binding domains with glycine and antagonist, 3-ethylphenyl-ACEPC
To Be Published
6OVE
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Crystal structure of GluN1/GluN2A NMDA receptor agonist binding domains with glycine and antagonist, 4-propylphenyl-ACEPC
分子名称: (3R,5S)-5-[(2R)-2-amino-2-carboxyethyl]-1-(4-propylphenyl)pyrazolidine-3-carboxylic acid, GLYCINE, Glutamate receptor ionotropic, ...
著者Syrenne, J.T, Mou, T.C, Tamborini, L, Pinto, A, Sprang, S.R, Hansen, K.B.
登録日2019-05-07
公開日2020-05-13
最終更新日2023-10-11
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Crystal structure of GluN1/GluN2A NMDA receptor agonist binding domains with glycine and antagonist, 3-ethylphenyl-ACEPC
To Be Published
1U0H
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BU of 1u0h by Molmil
STRUCTURAL BASIS FOR THE INHIBITION OF MAMMALIAN ADENYLYL CYCLASE BY MANT-GTP
分子名称: 3'-O-(N-METHYLANTHRANILOYL)-GUANOSINE-5'-TRIPHOSPHATE, 5'-GUANOSINE-DIPHOSPHATE-MONOTHIOPHOSPHATE, Adenylate cyclase, ...
著者Mou, T.C, Gille, A, Seifert, R.J, Sprang, S.R.
登録日2004-07-13
公開日2004-12-14
最終更新日2023-08-23
実験手法X-RAY DIFFRACTION (2.9 Å)
主引用文献Structural basis for the inhibition of mammalian membrane adenylyl cyclase by 2 '(3')-O-(N-Methylanthraniloyl)-guanosine 5 '-triphosphate.
J.Biol.Chem., 280, 2005
5I59
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Glutamate- and glycine-bound GluN1/GluN2A agonist binding domains with MPX 007
分子名称: 5-({[(3,4-difluorophenyl)sulfonyl]amino}methyl)-6-methyl-N-[(2-methyl-4H-1lambda~4~,3-thiazol-5-yl)methyl]pyrazine-2-carboxamide, GLUTAMIC ACID, GLYCINE, ...
著者Mou, T.-C, Sprang, S.R, Hansen, K.B.
登録日2016-02-14
公開日2016-09-21
最終更新日2023-09-27
実験手法X-RAY DIFFRACTION (2.25 Å)
主引用文献Structural Basis for Negative Allosteric Modulation of GluN2A-Containing NMDA Receptors.
Neuron, 91, 2016
5I57
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Glutamate- and glycine-bound GluN1/GluN2A agonist binding domains
分子名称: GLUTAMIC ACID, GLYCINE, Glutamate receptor ionotropic, ...
著者Mou, T.-C, Sprang, S.R, Hansen, K.B.
登録日2016-02-14
公開日2016-09-21
最終更新日2023-09-27
実験手法X-RAY DIFFRACTION (1.7 Å)
主引用文献Structural Basis for Negative Allosteric Modulation of GluN2A-Containing NMDA Receptors.
Neuron, 91, 2016
5I58
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GLUTAMATE- AND GLYCINE-BOUND GLUN1/GLUN2A AGONIST BINDING DOMAINS WITH MPX-004
分子名称: 5-({[(3-chloro-4-fluorophenyl)sulfonyl]amino}methyl)-N-[(2-methyl-1,3-thiazol-5-yl)methyl]pyrazine-2-carboxamide, GLUTAMIC ACID, GLYCINE, ...
著者Mou, T.-C, Sprang, S.R, Hansen, K.B.
登録日2016-02-14
公開日2016-09-21
最終更新日2023-09-27
実験手法X-RAY DIFFRACTION (2.52 Å)
主引用文献Structural Basis for Negative Allosteric Modulation of GluN2A-Containing NMDA Receptors.
Neuron, 91, 2016
5JTY
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Glutamate- and DCKA-bound GluN1/GluN2A agonist binding domains with MPX-007
分子名称: 4-hydroxy-5,7-dimethylquinoline-2-carboxylic acid, 5-({[(3,4-difluorophenyl)sulfonyl]amino}methyl)-6-methyl-N-[(2-methyl-1,3-thiazol-5-yl)methyl]pyrazine-2-carboxamide, GLUTAMIC ACID, ...
著者Mou, T.-C, Sprang, S.R, Hansen, K.B.
登録日2016-05-10
公開日2016-09-21
最終更新日2023-09-27
実験手法X-RAY DIFFRACTION (2.72 Å)
主引用文献Structural Basis for Negative Allosteric Modulation of GluN2A-Containing NMDA Receptors.
Neuron, 91, 2016
2GVZ
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Crystal Structure of Complex of Gs- with The Catalytic Domains of Mammalian Adenylyl Cyclase: Complex with MANT-ATP and Mn
分子名称: 3'-O-[2-(METHYLAMINO)BENZOYL]ADENOSINE 5'-(TETRAHYDROGEN TRIPHOSPHATE), 5'-GUANOSINE-DIPHOSPHATE-MONOTHIOPHOSPHATE, Adenylate cyclase type 2, ...
著者Mou, T.-C, Sprang, S.R.
登録日2006-05-03
公開日2006-07-04
最終更新日2023-08-30
実験手法X-RAY DIFFRACTION (3.27 Å)
主引用文献Broad specificity of Mammalian adenylyl cyclase for interaction with 2',3'-substituted purine- and pyrimidine nucleotide inhibitors.
Mol.Pharmacol., 70, 2006
2GVD
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Complex Of Gs- With The Catalytic Domains Of Mammalian Adenylyl Cyclase: Complex With TNP-ATP and Mn
分子名称: 5'-GUANOSINE-DIPHOSPHATE-MONOTHIOPHOSPHATE, Adenylate cyclase type 2, Adenylate cyclase type 5, ...
著者Mou, T.-C, Sprang, S.R.
登録日2006-05-02
公開日2006-07-04
最終更新日2023-08-30
実験手法X-RAY DIFFRACTION (2.9 Å)
主引用文献Broad specificity of Mammalian adenylyl cyclase for interaction with 2',3'-substituted purine- and pyrimidine nucleotide inhibitors.
Mol.Pharmacol., 70, 2006
2FGF
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THREE-DIMENSIONAL STRUCTURE OF HUMAN BASIC FIBROBLAST GROWTH FACTOR, A STRUCTURAL HOMOLOG OF INTERLEUKIN 1BETA
分子名称: HEPARIN-BINDING GROWTH FACTOR 2 PRECURSOR, SULFATE ION
著者Zhang, J, Sprang, S.R.
登録日1991-02-19
公開日1992-01-15
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (1.77 Å)
主引用文献Three-dimensional structure of human basic fibroblast growth factor, a structural homolog of interleukin 1 beta.
Proc.Natl.Acad.Sci.USA, 88, 1991
7RLE
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Crystal structure of PPAR gamma in complex with CREB-binding protein and agonist GW1929
分子名称: (2~{S})-3-[4-[2-[methyl(pyridin-2-yl)amino]ethoxy]phenyl]-2-[[2-(phenylcarbonyl)phenyl]amino]propanoic acid, CREB-binding protein, Peroxisome proliferator-activated receptor gamma
著者Nemetchek, M.D, Sprang, S.R, Hughes, T.S.
登録日2021-07-23
公開日2022-08-03
最終更新日2023-10-25
実験手法X-RAY DIFFRACTION (2.5 Å)
主引用文献A structural mechanism of nuclear receptor biased agonism.
Proc.Natl.Acad.Sci.USA, 119, 2022

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