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2DX0
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Crystal structure of the N-terminal SH2 domain of mouse phospholipase C-gamma 2
分子名称: Phospholipase C, gamma 2, SULFATE ION
著者Handa, N, Takagi, T, Murayama, K, Terada, T, Shirouzu, M, Yokoyama, S, RIKEN Structural Genomics/Proteomics Initiative (RSGI)
登録日2006-08-22
公開日2007-09-04
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (2.5 Å)
主引用文献Crystal structure of the N-terminal SH2 domain of mouse phospholipase C-gamma 2
To be Published
3HMO
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BU of 3hmo by Molmil
Crystal structure of human Mps1 catalytic domain in complex with the inhibitor staurosporine
分子名称: 2-(2-(2-(2-(2-(2-ETHOXYETHOXY)ETHOXY)ETHOXY)ETHOXY)ETHOXY)ETHANOL, Dual specificity protein kinase TTK, GLYCEROL, ...
著者Chu, M.L.H, Chavas, L.M.G, Williams, D.H, Tabernero, L, Eyers, P.A.
登録日2009-05-29
公開日2010-02-02
最終更新日2023-09-06
実験手法X-RAY DIFFRACTION (2.4 Å)
主引用文献Biophysical and X-ray crystallographic analysis of Mps1 kinase inhibitor complexes.
Biochemistry, 49, 2010
2DQI
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Crystal structure of hyhel-10 FV mutant (Ly50a) complexed with hen egg lysozyme
分子名称: Ig VH,anti-lysozyme, Lysozyme C, lysozyme binding Ig kappa chain V23-J2 region
著者Shiroishi, M, Kondo, H, Tsumoto, K, Kumagai, I.
登録日2006-05-26
公開日2007-01-23
最終更新日2023-10-25
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Structural consequences of mutations in interfacial Tyr residues of a protein antigen-antibody complex. The case of HyHEL-10-HEL
J.Biol.Chem., 282, 2007
1UOS
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BU of 1uos by Molmil
The Crystal Structure of the Snake Venom Toxin Convulxin
分子名称: CONVULXIN ALPHA, CONVULXIN BETA
著者Batuwangala, T, Leduc, M, Gibbins, J.M, Bon, C, Jones, E.Y.
登録日2003-09-22
公開日2003-10-14
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (2.7 Å)
主引用文献Structure of the Snake-Venom Toxin Convulxin
Acta Crystallogr.,Sect.D, 60, 2004
2VNY
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Structure of PKA-PKB chimera complexed with (1-(9H-Purin-6-yl) piperidin-4-yl)amine
分子名称: 1-(9H-purin-6-yl)piperidin-4-amine, CAMP-DEPENDENT PROTEIN KINASE INHIBITOR ALPHA, CAMP-DEPENDENT PROTEIN KINASE, ...
著者Caldwell, J.J, Davies, T.G, Donald, A, McHardy, T, Rowlands, M.G, Aherne, G.W, Hunter, L.K, Taylor, K, Ruddle, R, Raynaud, F.I, Verdonk, M, Workman, P, Garrett, M.D, Collins, I.
登録日2008-02-08
公開日2008-04-08
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (1.96 Å)
主引用文献Identification of 4-(4-Aminopiperidin-1-Yl)-7H-Pyrrolo[2,3-D]Pyrimidines as Selective Inhibitors of Protein Kinase B Through Fragment Elaboration.
J.Med.Chem., 51, 2008
2XKD
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BU of 2xkd by Molmil
Structure of Nek2 bound to aminopyrazine compound 12
分子名称: 4-[3-amino-6-(3,4,5-trimethoxyphenyl)pyrazin-2-yl]benzoic acid, CHLORIDE ION, SERINE/THREONINE-PROTEIN KINASE NEK2
著者Mas-Droux, C, Bayliss, R.
登録日2010-07-07
公開日2010-10-27
最終更新日2023-12-20
実験手法X-RAY DIFFRACTION (1.96 Å)
主引用文献Aminopyrazine Inhibitors Binding to an Unusual Inactive Conformation of the Mitotic Kinase Nek2: Sar and Structural Characterization.
J.Med.Chem., 53, 2010
2XM8
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Co-crystal structure of a small molecule inhibitor bound to the kinase domain of Chk2
分子名称: 2-{4-[(3S)-PYRROLIDIN-3-YLAMINO]QUINAZOLIN-2-YL}PHENOL, SERINE/THREONINE-PROTEIN KINASE CHK2
著者Caldwell, J.J, Welsh, E.J, Matijssen, C, Anderson, V.E, Antoni, L, Boxall, K, Urban, F, Hayes, A, Raynaud, F.I, Rigoreau, L.J, Raynham, T, Aherne, G.W, Pearl, L.H, Oliver, A.W, Garrett, M.D, Collins, I.
登録日2010-07-26
公開日2011-01-12
最終更新日2023-12-20
実験手法X-RAY DIFFRACTION (3.4 Å)
主引用文献Structure-Based Design of Potent and Selective 2-(Quinazolin-2-Yl)Phenol Inhibitors of Checkpoint Kinase 2.
J.Med.Chem., 54, 2011
3VBQ
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Exploitation of hydrogen bonding constraints and flat hydrophobic energy landscapes in Pim-1 kinase needle screening and inhibitor design
分子名称: (5~{Z})-5-[[3-[6-[(4-azanylcyclohexyl)amino]pyrazin-2-yl]phenyl]methylidene]-1,3-thiazolidine-2,4-dione, Serine/threonine-protein kinase pim-1
著者Liu, J.
登録日2012-01-02
公開日2012-03-21
最終更新日2024-02-28
実験手法X-RAY DIFFRACTION (1.85 Å)
主引用文献Implications of promiscuous Pim-1 kinase fragment inhibitor hydrophobic interactions for fragment-based drug design.
J.Med.Chem., 55, 2012
1SFI
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High resolution structure of a potent, cyclic protease inhibitor from sunflower seeds
分子名称: CALCIUM ION, SULFATE ION, TRYPSIN, ...
著者Luckett, S, Garcia, R.S, Barker, J.J, Konarev, A.V, Shewry, P, Clarke, A.R, Brady, R.L.
登録日1998-12-16
公開日1999-07-09
最終更新日2023-08-09
実験手法X-RAY DIFFRACTION (1.65 Å)
主引用文献High-resolution structure of a potent, cyclic proteinase inhibitor from sunflower seeds.
J.Mol.Biol., 290, 1999
1JJJ
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SOLUTION STRUCTURE OF RECOMBINANT HUMAN EPIDERMAL-TYPE FATTY ACID BINDING PROTEIN
分子名称: EPIDERMAL-TYPE FATTY ACID BINDING PROTEIN (E-FABP)
著者Gutierrez-Gonzalez, L.H, Ludwig, C, Hohoff, C, Rademacher, M, Hanhoff, T, Rueterjans, H, Spener, F, Luecke, C.
登録日2001-07-06
公開日2002-06-19
最終更新日2022-02-23
実験手法SOLUTION NMR
主引用文献Solution structure and backbone dynamics of human epidermal-type fatty acid-binding protein (E-FABP)
BIOCHEM.J., 364, 2002
2XMY
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Discovery and Characterisation of 2-Anilino-4-(thiazol-5-yl) pyrimidine Transcriptional CDK Inhibitors as Anticancer Agents
分子名称: 4-[4-(3,4-DIMETHYL-2-OXO-2,3-DIHYDRO-THIAZOL-5-YL)-PYRIMIDIN-2-YLAMINO]-N-(2-METHOXY-ETHYL)-BENZENESULFONAMIDE, CELL DIVISION PROTEIN KINASE 2
著者Wang, S, Griffiths, G, Midgley, C.A, Barnett, A.L, Cooper, M, Grabarek, J, Ingram, L, Jackson, W, Kontopidis, G, McClue, S.J, McInnes, C, McLachlan, J, Meades, C, Mezna, M, Stuart, I, Thomas, M.P, Zheleva, D.I, Lane, D.P, Jackson, R.C, Glover, D.M, Blake, D.G, Fischer, P.M.
登録日2010-07-29
公開日2010-11-10
最終更新日2023-12-20
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献Discovery and Characterisation of 2-Anilino-4-(Thiazol-5-Yl)Pyrimidine Transcriptional Cdk Inhibitors as Anticancer Agents
Chem.Biol., 17, 2010
2DHG
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Solution structure of the C-terminal RNA recognition motif in tRNA selenocysteine associated protein
分子名称: tRNA selenocysteine associated protein (SECP43)
著者Imai, T, Tsuda, K, Muto, Y, Inoue, M, Kigawa, T, Terada, T, Shirouzu, M, Yokoyama, S, RIKEN Structural Genomics/Proteomics Initiative (RSGI)
登録日2006-03-23
公開日2006-09-23
最終更新日2024-05-29
実験手法SOLUTION NMR
主引用文献Solution structure of the C-terminal RNA recognition motif in tRNA selenocysteine associated protein
To be Published
3HRC
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BU of 3hrc by Molmil
Crystal structure of a mutant of human PDK1 Kinase domain in complex with ATP
分子名称: 3-phosphoinositide-dependent protein kinase 1, ADENOSINE-5'-TRIPHOSPHATE
著者Hindie, V, Alzari, P.M, Biondi, R.M.
登録日2009-06-09
公開日2009-09-15
最終更新日2023-11-01
実験手法X-RAY DIFFRACTION (1.91 Å)
主引用文献Structure and allosteric effects of low-molecular-weight activators on the protein kinase PDK1.
Nat.Chem.Biol., 5, 2009
1UVZ
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structure of human thioredoxin 2
分子名称: THIOREDOXIN
著者Smeets, A, Evrard, C, Declercq, J.P.
登録日2004-01-27
公開日2005-06-16
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (2.01 Å)
主引用文献Crystal Structures of Oxidized and Reduced Forms of Human Mitochondrial Thioredoxin 2.
Protein Sci., 14, 2005
2DJU
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Solution structures of the fn3 domain of human receptor-type tyrosine-protein phosphatase F
分子名称: Receptor-type tyrosine-protein phosphatase F
著者Sato, M, Koshiba, S, Inoue, M, Kigawa, T, Yokoyama, S, RIKEN Structural Genomics/Proteomics Initiative (RSGI)
登録日2006-04-05
公開日2006-10-05
最終更新日2024-05-29
実験手法SOLUTION NMR
主引用文献Solution structures of the fn3 domain of human receptor-type tyrosine-protein phosphatase F
to be published
2DLK
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BU of 2dlk by Molmil
Solution structure of the first and the second zf-C2H2 domains of zinc finger protein 692
分子名称: ZINC ION, novel protein
著者Zhang, H.P, Nagashima, T, Hayashi, F, Yokoyama, S, RIKEN Structural Genomics/Proteomics Initiative (RSGI)
登録日2006-04-20
公開日2006-10-20
最終更新日2024-05-29
実験手法SOLUTION NMR
主引用文献Solution structure of the first and the second zf-C2H2 domains of zinc finger protein 692
To be published
2DM0
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BU of 2dm0 by Molmil
Solution structure of the SH2 domain of human Tyrosine-protein kinase TXK
分子名称: Tyrosine-protein kinase TXK
著者Endo, H, Hayashi, F, Yoshida, M, Yokoyama, S, RIKEN Structural Genomics/Proteomics Initiative (RSGI)
登録日2006-04-20
公開日2006-10-20
最終更新日2024-05-29
実験手法SOLUTION NMR
主引用文献Solution structure of the SH2 domain of human Tyrosine-protein kinase TXK
To be Published
1JZK
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BU of 1jzk by Molmil
Crystal Structure of Scapharca inaequivalvis HbI, I114F mutant (deoxy)
分子名称: GLOBIN I - ARK SHELL, PROTOPORPHYRIN IX CONTAINING FE
著者Knapp, J.E, Gibson, Q.H, Cushing, L, Royer Jr, W.E.
登録日2001-09-16
公開日2001-12-19
最終更新日2023-08-16
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献Restricting the Ligand-Linked Heme Movement in Scapharca Dimeric Hemoglobin Reveals Tight Coupling between Distal and Proximal Contributions to Cooperativity.
Biochemistry, 40, 2001
2DML
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The solution structure of the first thioredoxin domain of mouse Protein disulfide-isomerase A6
分子名称: Protein disulfide-isomerase A6
著者Tochio, N, Koshiba, S, Inoue, M, Kigawa, T, Yokoyama, S, RIKEN Structural Genomics/Proteomics Initiative (RSGI)
登録日2006-04-22
公開日2006-10-22
最終更新日2024-05-29
実験手法SOLUTION NMR
主引用文献The solution structure of the first thioredoxin domain of mouse Protein disulfide-isomerase A6
To be Published
1UZ2
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The Cys121Ser Mutant of Beta-Lactoglobulin
分子名称: BETA-LACTOGLOBULIN
著者McNae, I, Jayat, D, Haertle, T, Holt, C, Sawyer, L.
登録日2004-03-03
公開日2004-05-20
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (1.95 Å)
主引用文献A recombinant C121S mutant of bovine beta-lactoglobulin is more susceptible to peptic digestion and to denaturation by reducing agents and heating.
Biochemistry, 43, 2004
2Y0A
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Structure of DAPK1 construct residues 1-304
分子名称: 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, DEATH-ASSOCIATED PROTEIN KINASE 1
著者Yumerefendi, H, Mas, P.J, Dordevic, N, McCarthy, A.A, Hart, D.J.
登録日2010-12-01
公開日2011-12-14
最終更新日2023-12-20
実験手法X-RAY DIFFRACTION (2.6 Å)
主引用文献Library-Based Construct Screening of Death-Associated Protein Kinase 1 Identifies the Minimal Calmodulin Interaction Region and Autoinhibitory Conformation of the Catalytic Domain
To be Published
1UYU
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Xenon COMPLEX OF wildtype P450CAM FROM PSEUDOMONAS PUTIDA
分子名称: CAMPHOR, CYTOCHROME P450-CAM, POTASSIUM ION, ...
著者Wade, R.C, Winn, P.J, Schlichting, I, Sudarko, X.
登録日2004-03-02
公開日2005-03-07
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献A Survey of Active Site Access Channels in Cytochromes P450
J.Inorg.Biochem., 98, 2004
2DQG
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Crystal structure of hyhel-10 FV mutant (Hy53f) complexed with hen egg lysozyme
分子名称: Ig VH,anti-lysozyme, Lysozyme C, lysozyme binding Ig kappa chain V23-J2 region
著者Shiroishi, M, Kondo, H, Tsumoto, K, Kumagai, I.
登録日2006-05-25
公開日2007-01-23
最終更新日2023-10-25
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Structural consequences of mutations in interfacial Tyr residues of a protein antigen-antibody complex. The case of HyHEL-10-HEL
J.Biol.Chem., 282, 2007
2DGW
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Solution structure of the second RNA recognition motif in RNA-binding protein 19
分子名称: Probable RNA-binding protein 19
著者Abe, C, Muto, Y, Inoue, M, Kigawa, T, Terada, T, Shirouzu, M, Yokoyama, S, RIKEN Structural Genomics/Proteomics Initiative (RSGI)
登録日2006-03-16
公開日2006-09-16
最終更新日2024-05-29
実験手法SOLUTION NMR
主引用文献Solution structure of the second RNA recognition motif in RNA-binding protein 19
To be Published
1UTJ
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Trypsin specificity as elucidated by LIE calculations, X-ray structures and association constant measurements
分子名称: BENZYLAMINE, CALCIUM ION, TRYPSIN I
著者Leiros, H.-K.S, Brandsdal, B.O, Andersen, O.A, Os, V, Leiros, I, Helland, R, Otlewski, J, Willassen, N.P, Smalas, A.O.
登録日2003-12-09
公開日2004-01-15
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (1.83 Å)
主引用文献Trypsin Specificity as Elucidated by Lie Calculations, X-Ray Structures, and Association Constant Measurements
Protein Sci., 13, 2004

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件を2024-08-07に公開中

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