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1Y7O
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BU of 1y7o by Molmil
The structure of Streptococcus pneumoniae A153P ClpP
分子名称: ATP-dependent Clp protease proteolytic subunit, CALCIUM ION
著者Kimber, M.S, Gribun, A, Ching, R, Sprangers, R, Fiebig, K.M, Houry, W.A.
登録日2004-12-09
公開日2005-02-08
最終更新日2023-11-15
実験手法X-RAY DIFFRACTION (2.51 Å)
主引用文献The ClpP double ring tetradecameric protease exhibits plastic ring-ring interactions, and the N termini of its subunits form flexible loops that are essential for ClpXP and ClpAP complex formation.
J.Biol.Chem., 280, 2005
7N2W
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BU of 7n2w by Molmil
The crystal structure of an FMN-dependent NADH-azoreductase, AzoA in complex with Red 40
分子名称: 6-hydroxy-5-[(E)-(2-methoxy-5-methyl-4-sulfophenyl)diazenyl]naphthalene-2-sulfonic acid, FLAVIN MONONUCLEOTIDE, FMN dependent NADH:quinone oxidoreductase
著者Arcinas, A.J, Fedorov, E, Kelly, L, Almo, S.C, Ghosh, A.
登録日2021-05-30
公開日2022-06-01
最終更新日2023-10-18
実験手法X-RAY DIFFRACTION (2.65 Å)
主引用文献Uncovering a novel mechanism of enzyme activation in multimeric azoreductases
To Be Published
7N2X
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BU of 7n2x by Molmil
The crystal structure of an FMN-dependent NADH:quinone oxidoreductase, AzoR from Escherichia coli
分子名称: 1,2-ETHANEDIOL, 1-ETHOXY-2-(2-ETHOXYETHOXY)ETHANE, 2-AMINO-ACRYLIC ACID, ...
著者Arcinas, A.J, Fedorov, E, Kelly, L, Almo, S.C, Ghosh, A.
登録日2021-05-30
公開日2022-08-31
最終更新日2023-10-18
実験手法X-RAY DIFFRACTION (1.7 Å)
主引用文献Uncovering a novel mechanism of enzyme activation in multimeric azoreductases
To Be Published
4ZJW
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BU of 4zjw by Molmil
RORgamma in complex with inverse agonist 16
分子名称: 4-chloro-3-[1-(2-chloro-6-fluorobenzoyl)-1,2,3,4-tetrahydroquinolin-6-yl]-N-methylbenzamide, Nuclear receptor ROR-gamma
著者Marcotte, D.J.
登録日2015-04-29
公開日2015-06-17
最終更新日2023-09-27
実験手法X-RAY DIFFRACTION (2.5 Å)
主引用文献Discovery of biaryl carboxylamides as potent ROR gamma inverse agonists.
Bioorg.Med.Chem.Lett., 25, 2015
4ZJR
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BU of 4zjr by Molmil
RORgamma in complex with inverse agonist 48
分子名称: 6-chloro-4'-[(2-chloro-6-fluorobenzoyl)(methyl)amino]-3'-(2,2,2-trifluoroethoxy)biphenyl-3-carboxamide, Nuclear receptor ROR-gamma
著者Marcotte, D.J.
登録日2015-04-29
公開日2015-06-17
最終更新日2023-09-27
実験手法X-RAY DIFFRACTION (2.702 Å)
主引用文献Discovery of biaryl carboxylamides as potent ROR gamma inverse agonists.
Bioorg.Med.Chem.Lett., 25, 2015
5FWN
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BU of 5fwn by Molmil
Imine Reductase from Amycolatopsis orientalis. Closed form in in complex with (R)- Methyltetrahydroisoquinoline
分子名称: (1R)-1-methyl-1,2,3,4-tetrahydroisoquinoline, IMINE REDUCTASE, NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, ...
著者Man, H, Aleku, G, Turner, N.J, Grogan, G.
登録日2016-02-18
公開日2016-06-01
最終更新日2024-01-10
実験手法X-RAY DIFFRACTION (2.14 Å)
主引用文献Stereoselectivity and Structural Characterization of an Imine Reductase (Ired) from Amycolatopsis Orientalis
Acs Catalysis, 6, 2016
5A9S
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NADPH complex of Imine Reductase from Amycolatopsis orientalis
分子名称: CALCIUM ION, IMINE REDUCTASE, NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE
著者Man, H, Aleku, G, Turner, N.J, Grogan, G.
登録日2015-07-22
公開日2016-06-01
最終更新日2024-01-10
実験手法X-RAY DIFFRACTION (2.06 Å)
主引用文献Stereoselectivity and Structural Characterization of an Imine Reductase (IRED) from Amycolatopsis orientalis
Acs Catalysis, 6, 2016
5A9R
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Apo form of Imine reductase from Amycolatopsis orientalis
分子名称: ACETATE ION, IMINE REDUCTASE
著者Man, H, Aleku, G, Turner, N.J, Grogan, G.
登録日2015-07-22
公開日2016-06-01
最終更新日2024-01-10
実験手法X-RAY DIFFRACTION (1.55 Å)
主引用文献Stereoselectivity and Structural Characterization of an Imine Reductase (Ired) from Amycolatopsis Orientalis
Acs Catalysis, 6, 2016
5A9T
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BU of 5a9t by Molmil
Imine Reductase from Amycolatopsis orientalis in complex with (R)- Methyltetrahydroisoquinoline
分子名称: (1R)-1-methyl-1,2,3,4-tetrahydroisoquinoline, ACETATE ION, CALCIUM ION, ...
著者Man, H, Aleku, G, Turner, N.J, Grogan, G.
登録日2015-07-22
公開日2016-06-01
最終更新日2024-01-10
実験手法X-RAY DIFFRACTION (1.5 Å)
主引用文献Stereoselectivity and Structural Characterization of an Imine Reductase (Ired) from Amycolatopsis Orientalis
Acs Catalysis, 6, 2016
2R4F
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Substituted Pyrazoles as Hepatselective HMG-COA reductase inhibitors
分子名称: (3R,5R)-7-[1-(4-fluorophenyl)-4-(1-methylethyl)-3-{methyl[(1R)-1-phenylethyl]carbamoyl}-1H-pyrazol-5-yl]-3,5-dihydroxyheptanoic acid, 3-hydroxy-3-methylglutaryl-coenzyme A reductase, SULFATE ION
著者Pavlovsky, A, Pfefferkorn, J.A, Harris, M.S, Finzel, B.C.
登録日2007-08-31
公開日2008-04-29
最終更新日2024-02-21
実験手法X-RAY DIFFRACTION (1.7 Å)
主引用文献Substituted pyrazoles as hepatoselective HMG-CoA reductase inhibitors: discovery of (3R,5R)-7-[2-(4-fluoro-phenyl)-4-isopropyl-5-(4-methyl-benzylcarbamoyl)-2H-pyrazol-3-yl]-3,5-dihydroxyheptanoic acid (PF-3052334) as a candidate for the treatment of hypercholesterolemia.
J.Med.Chem., 51, 2008

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件を2024-10-16に公開中

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