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2QMZ
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Quinone Reductase 2 in Complex with Dopamine
分子名称: FLAVIN-ADENINE DINUCLEOTIDE, L-DOPAMINE, Ribosyldihydronicotinamide dehydrogenase, ...
著者Fu, Y, Buryanovskyy, L, Zhang, Z.
登録日2007-07-17
公開日2008-06-24
最終更新日2024-02-21
実験手法X-RAY DIFFRACTION (2.1 Å)
主引用文献Quinone Reductase 2 Regulates Catecholamine Oxidation
To be Published
2R0L
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BU of 2r0l by Molmil
Short Form HGFA with Inhibitory Fab75
分子名称: Hepatocyte growth factor activator, antibody heavy chain, Fab portion only, ...
著者Eigenbrot, C, Shia, S.
登録日2007-08-20
公開日2007-12-25
最終更新日2023-08-30
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献Structural insight into distinct mechanisms of protease inhibition by antibodies.
Proc.Natl.Acad.Sci.Usa, 104, 2007
2R05
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Crystal Structure of ALIX/AIP1 in complex with the HIV-1 YPLASL Late Domain
分子名称: Programmed cell death 6-interacting protein, p6-Gag
著者Hill, C.P, Zhai, Q, Fisher, R.D.
登録日2007-08-17
公開日2007-12-18
最終更新日2024-02-21
実験手法X-RAY DIFFRACTION (2.55 Å)
主引用文献Structural and functional studies of ALIX interactions with YPX(n)L late domains of HIV-1 and EIAV.
Nat.Struct.Mol.Biol., 15, 2008
2R1U
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DJ-1 activation by catechol quinone modification
分子名称: Protein DJ-1
著者Zhongtao, Z, Yue, F.
登録日2007-08-23
公開日2008-08-26
最終更新日2024-02-21
実験手法X-RAY DIFFRACTION (1.5 Å)
主引用文献DJ-1 activation by catechol quinone modification
To be Published
2R2M
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2-(2-Chloro-6-Fluorophenyl)Acetamides as Potent Thrombin Inhibitors
分子名称: Hirudin-3A, N-[2-({[amino(imino)methyl]amino}oxy)ethyl]-2-{6-chloro-3-[(2,2-difluoro-2-phenylethyl)amino]-2-fluorophenyl}acetamide, Thrombin heavy chain, ...
著者Spurlino, J.
登録日2007-08-27
公開日2008-08-26
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (2.1 Å)
主引用文献2-(2-Chloro-6-Fluorophenyl)Acetamides as Potent Thrombin Inhibitors
Bioorg.Med.Chem.Lett., 17, 2007
2O48
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Crystal structure of Mammalian Dimeric Dihydrodiol Dehydrogenase
分子名称: BETA-MERCAPTOETHANOL, Dimeric dihydrodiol dehydrogenase, P-HYDROXYACETOPHENONE, ...
著者Carbone, V, El-Kabbani, O.
登録日2006-12-04
公開日2007-07-31
最終更新日2023-12-27
実験手法X-RAY DIFFRACTION (2.59 Å)
主引用文献Structures of dimeric dihydrodiol dehydrogenase apoenzyme and inhibitor complex: probing the subunit interface with site-directed mutagenesis.
Proteins, 70, 2008
2OHQ
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X-ray crystal structure of beta secretase complexed with compound 4
分子名称: 6-[2-(3'-METHOXYBIPHENYL-3-YL)ETHYL]PYRIDIN-2-AMINE, Beta-secretase 1, DIMETHYL SULFOXIDE, ...
著者Patel, S.
登録日2007-01-10
公開日2007-03-13
最終更新日2023-08-30
実験手法X-RAY DIFFRACTION (2.1 Å)
主引用文献Application of fragment screening by X-ray crystallography to the discovery of aminopyridines as inhibitors of beta-secretase.
J.Med.Chem., 50, 2007
2OHT
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X-ray crystal structure of beta secretase complexed with compound 7
分子名称: Beta-secretase 1, DIMETHYL SULFOXIDE, IODIDE ION, ...
著者Patel, S.
登録日2007-01-10
公開日2007-03-13
最終更新日2023-08-30
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Application of fragment screening by X-ray crystallography to the discovery of aminopyridines as inhibitors of beta-secretase.
J.Med.Chem., 50, 2007
2R3G
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Crystal Structure of Cyclin-Dependent Kinase 2 with inhibitor
分子名称: 6-(2-fluorophenyl)-N-(pyridin-3-ylmethyl)imidazo[1,2-a]pyrazin-8-amine, Cell division protein kinase 2
著者Fischmann, T.O, Hruza, A.W, Madison, V.M, Duca, J.S.
登録日2007-08-29
公開日2008-01-22
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (1.55 Å)
主引用文献Structure-guided discovery of cyclin-dependent kinase inhibitors.
Biopolymers, 89, 2008
2QLF
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Crystal Structure of Caspase-7 with inhibitor AC-DNLD-CHO
分子名称: Caspase-7, Inhibitor AC-DNLD-CHO, Peptide QGHGE
著者Agniswamy, J, Fang, B, Weber, I.
登録日2007-07-12
公開日2007-08-28
最終更新日2023-11-15
実験手法X-RAY DIFFRACTION (2.8 Å)
主引用文献Plasticity of S2-S4 specificity pockets of executioner caspase-7 revealed by structural and kinetic analysis.
Febs J., 274, 2007
2QOS
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Crystal structure of complement protein C8 in complex with a peptide containing the C8 binding site on C8
分子名称: Complement component 8, gamma polypeptide, Complement component C8 alpha chain
著者Lovelace, L.L, Chiswell, B, Slade, D.J, Sodetz, J.M, Lebioda, L.
登録日2007-07-20
公開日2007-10-16
最終更新日2023-08-30
実験手法X-RAY DIFFRACTION (1.81 Å)
主引用文献Crystal structure of complement protein C8gamma in complex with a peptide containing the C8gamma binding site on C8alpha: Implications for C8gamma ligand binding.
Mol.Immunol., 45, 2008
2R0N
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The effect of a Glu370Asp mutation in Glutaryl-CoA Dehydrogenase on Proton Transfer to the Dienolate Intermediate
分子名称: 3-thiaglutaryl-CoA, FLAVIN-ADENINE DINUCLEOTIDE, Glutaryl-CoA dehydrogenase
著者Rao, K.S, Albro, M, Fu, Z, Narayanan, B, Baddam, S, Lee, H.J, Kim, J.J, Frerman, F.E.
登録日2007-08-20
公開日2008-04-22
最終更新日2023-08-30
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献The effect of a Glu370Asp mutation in glutaryl-CoA dehydrogenase on proton transfer to the dienolate intermediate.
Biochemistry, 46, 2007
2QUY
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Truncated mutant ASN175ALA of penicillin v acylase from bacillus sphaericus
分子名称: CHLORIDE ION, Penicillin acylase
著者Pathak, M.C, Brannigan, J, Dodson, G.G, Suresh, C.G.
登録日2007-08-07
公開日2008-08-26
最終更新日2024-05-29
実験手法X-RAY DIFFRACTION (1.7 Å)
主引用文献Auto-proteolytic processing of Penicillin V Acylase is simpler than of other related Ntn hydrolases
To be Published
2QE4
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Estrogen receptor alpha ligand-binding domain in complex with a benzopyran agonist
分子名称: (3AS,4R,9BR)-4-(4-HYDROXYPHENYL)-6-(METHOXYMETHYL)-1,2,3,3A,4,9B-HEXAHYDROCYCLOPENTA[C]CHROMEN-8-OL, Estrogen receptor
著者Norman, B.H, Richardson, T.I, Dodge, J.A, Pfeifer, L.A, Durst, G.L, Wang, Y, Durbin, J.D, Krishnan, V, Dinn, S.R, Liu, S.Q, Reilly, J.E, Ryter, K.T.
登録日2007-06-22
公開日2007-09-04
最終更新日2024-02-21
実験手法X-RAY DIFFRACTION (2.4 Å)
主引用文献Benzopyrans as selective estrogen receptor beta agonists (SERBAs). Part 4: Functionalization of the benzopyran A-ring.
Bioorg.Med.Chem.Lett., 17, 2007
2QLJ
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Crystal Structure of Caspase-7 with Inhibitor AC-WEHD-CHO
分子名称: CITRIC ACID, Caspase-7, Inhibitor AC-WEHD-CHO, ...
著者Agniswamy, J, Fang, B, Weber, I.
登録日2007-07-12
公開日2007-08-28
最終更新日2023-11-15
実験手法X-RAY DIFFRACTION (2.6 Å)
主引用文献Plasticity of S2-S4 specificity pockets of executioner caspase-7 revealed by structural and kinetic analysis.
Febs J., 274, 2007
2QL5
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Crystal Structure of caspase-7 with inhibitor AC-DMQD-CHO
分子名称: CITRIC ACID, Caspase-7, inhibitor, ...
著者Agniswamy, J, Fang, B, Weber, I.
登録日2007-07-12
公開日2007-08-28
最終更新日2023-11-15
実験手法X-RAY DIFFRACTION (2.34 Å)
主引用文献Plasticity of S2-S4 specificity pockets of executioner caspase-7 revealed by structural and kinetic analysis.
Febs J., 274, 2007
2QL9
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Crystal Structure of Caspase-7 with inhibitor AC-DQMD-CHO
分子名称: CITRIC ACID, Caspase-7, Inhibitor AC-DQMD-CHO, ...
著者Agniswamy, J, Fang, B, Weber, I.
登録日2007-07-12
公開日2007-08-28
最終更新日2023-11-15
実験手法X-RAY DIFFRACTION (2.14 Å)
主引用文献Plasticity of S2-S4 specificity pockets of executioner caspase-7 revealed by structural and kinetic analysis.
Febs J., 274, 2007
2QFD
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Crystal structure of the regulatory domain of human RIG-I with bound Hg
分子名称: MERCURY (II) ION, Probable ATP-dependent RNA helicase DDX58
著者Cui, S, Lammens, A, Lammens, K, Hopfner, K.P.
登録日2007-06-27
公開日2008-02-12
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (2.7 Å)
主引用文献The C-Terminal Regulatory Domain Is the RNA 5'-Triphosphate Sensor of RIG-I.
Mol.Cell, 29, 2008
2QKA
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Structural and Kinetic Study of the Differences between Human and E.coli Manganese Superoxide Dismutases
分子名称: MANGANESE (II) ION, Superoxide dismutase [Mn]
著者Zheng, J, Domsic, J.F, Cabelli, D, McKenna, R, Silverman, D.N.
登録日2007-07-10
公開日2008-07-29
最終更新日2023-08-30
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献Structural and kinetic study of differences between human and Escherichia coli manganese superoxide dismutases.
Biochemistry, 46, 2007
2QKI
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Human C3c in complex with the inhibitor compstatin
分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, BROMIDE ION, Complement C3, ...
著者Janssen, B.J.C, Halff, E.F, Lambris, J.D, Gros, P.
登録日2007-07-11
公開日2007-08-14
最終更新日2023-08-30
実験手法X-RAY DIFFRACTION (2.4 Å)
主引用文献Structure of compstatin in complex with complement component C3c reveals a new mechanism of complement inhibition.
J.Biol.Chem., 282, 2007
2QMY
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Quinone Reductase 2 in complex with adrenochrome
分子名称: (3S)-3-hydroxy-1-methyl-2,3-dihydro-1H-indole-5,6-dione, FLAVIN-ADENINE DINUCLEOTIDE, Ribosyldihydronicotinamide dehydrogenase, ...
著者Zhang, Z, Fu, Y, Buryanovskky, L.
登録日2007-07-17
公開日2008-06-24
最終更新日2024-02-21
実験手法X-RAY DIFFRACTION (2.5 Å)
主引用文献Quinone Reductase 2 regulates Catecholamine oxidation
To be Published
2QKH
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Crystal structure of the extracellular domain of human GIP receptor in complex with the hormone GIP
分子名称: Cyclic 2,3-di-O-methyl-alpha-D-glucopyranose-(1-4)-2-O-methyl-alpha-D-glucopyranose-(1-4)-2,6-di-O-methyl-alpha-D-glucopyranose-(1-4)-2-O-methyl-alpha-D-glucopyranose-(1-4)-alpha-D-glucopyranose-(1-4)-alpha-D-glucopyranose-(1-4)-3-O-methyl-alpha-D-glucopyranose, D(-)-TARTARIC ACID, Glucose-dependent insulinotropic polypeptide, ...
著者Parthier, C, Kleinschmidt, M, Neumann, P, Rudolph, R, Manhart, S, Schlenzig, D, Fanghanel, J, Rahfeld, J.-U, Demuth, H.-U, Stubbs, M.T.
登録日2007-07-11
公開日2007-08-14
最終更新日2020-07-29
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献Crystal structure of the incretin-bound extracellular domain of a G protein-coupled receptor
Proc.Natl.Acad.Sci.Usa, 104, 2007
2QU6
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Crystal structure of the VEGFR2 kinase domain in complex with a benzoxazole inhibitor
分子名称: 4-({2-[(4-chloro-3-{[(2S)-1-methylpyrrolidin-2-yl]methoxy}phenyl)amino]-1,3-benzoxazol-5-yl}oxy)-N-methylpyridine-2-carboxamide, SULFATE ION, Vascular endothelial growth factor receptor 2
著者Whittington, D.A, Kim, J.L, Long, A.M, Rose, P, Gu, Y, Zhao, H.
登録日2007-08-03
公開日2007-09-25
最終更新日2024-02-21
実験手法X-RAY DIFFRACTION (2.1 Å)
主引用文献Design, Synthesis, and Evaluation of Orally Active Benzimidazoles and Benzoxazoles as Vascular Endothelial Growth Factor-2 Receptor Tyrosine Kinase Inhibitors.
J.Med.Chem., 50, 2007
2QQR
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JMJD2A hybrid tudor domains
分子名称: JmjC domain-containing histone demethylation protein 3A, SULFATE ION
著者Lee, J, Botuyan, M.V, Mer, G.
登録日2007-07-26
公開日2007-12-11
最終更新日2023-11-15
実験手法X-RAY DIFFRACTION (1.8 Å)
主引用文献Distinct binding modes specify the recognition of methylated histones H3K4 and H4K20 by JMJD2A-tudor.
Nat.Struct.Mol.Biol., 15, 2008
2R02
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Crystal Structure of ALIX/AIP1 in complex with the HIV-1 YPLTSL Late Domain
分子名称: Programmed cell death 6-interacting protein, p6-gag
著者Hill, C.P, Zhai, Q, Fisher, R.D.
登録日2007-08-17
公開日2007-12-18
最終更新日2024-02-21
実験手法X-RAY DIFFRACTION (2.6 Å)
主引用文献Structural and functional studies of ALIX interactions with YPX(n)L late domains of HIV-1 and EIAV.
Nat.Struct.Mol.Biol., 15, 2008

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