2OOS
| |
2OOT
| |
2OOV
| |
2OOW
| MIF Bound to a Fluorinated OXIM Derivative | 分子名称: | 3-FLUORO-4-HYDROXYBENZALDEHYDE O-(CYCLOHEXYLCARBONYL)OXIME, GLYCEROL, ISOPROPYL ALCOHOL, ... | 著者 | Crichlow, G.V, Al-Abed, Y, Lolis, E. | 登録日 | 2007-01-26 | 公開日 | 2007-06-05 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (1.75 Å) | 主引用文献 | Alternative chemical modifications reverse the binding orientation of a pharmacophore scaffold in the active site of macrophage migration inhibitory factor. J.Biol.Chem., 282, 2007
|
|
2OOX
| |
2OOY
| |
2OOZ
| Macrophage Migration Inhibitory Factor (MIF) Complexed with OXIM6 (an OXIM Derivative Not Containing a Ring in its R-group) | 分子名称: | 4-HYDROXYBENZALDEHYDE O-(3,3-DIMETHYLBUTANOYL)OXIME, GLYCEROL, ISOPROPYL ALCOHOL, ... | 著者 | Crichlow, G.V, Al-Abed, Y, Lolis, E. | 登録日 | 2007-01-26 | 公開日 | 2007-06-05 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | 主引用文献 | Alternative chemical modifications reverse the binding orientation of a pharmacophore scaffold in the active site of macrophage migration inhibitory factor. J.Biol.Chem., 282, 2007
|
|
2OP0
| Crystal structure of plasmodium falciparum enoyl ACP reductase with triclosan reductase | 分子名称: | 2-[4-(AMINOMETHYL)-2-CHLOROPHENOXY]-5-PYRIDIN-2-YLPHENOL, Enoyl-acyl carrier reductase, NICOTINAMIDE-ADENINE-DINUCLEOTIDE, ... | 著者 | Tsai, H. | 登録日 | 2007-01-26 | 公開日 | 2007-07-17 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (2.8 Å) | 主引用文献 | X-ray structural analysis of Plasmodium falciparum enoyl acyl carrier protein reductase as a pathway toward the optimization of triclosan antimalarial efficacy J.Biol.Chem., 282, 2007
|
|
2OP1
| Crystal structure of plasmodium falciparum enoyl ACP reductase with triclosan reductase | 分子名称: | 2-(2,4-DICHLOROPHENOXY)-5-(PYRIDIN-2-YLMETHYL)PHENOL, Enoyl-acyl carrier reductase, NICOTINAMIDE-ADENINE-DINUCLEOTIDE | 著者 | Tsai, H. | 登録日 | 2007-01-26 | 公開日 | 2007-07-17 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (2.6 Å) | 主引用文献 | X-ray structural analysis of Plasmodium falciparum enoyl acyl carrier protein reductase as a pathway toward the optimization of triclosan antimalarial efficacy J.Biol.Chem., 282, 2007
|
|
2OP2
| |
2OP3
| The structure of cathepsin S with a novel 2-arylphenoxyacetaldehyde inhibitor derived by the Substrate Activity Screening (SAS) method | 分子名称: | 2,5,8,11,14,17,20,23,26,29,32,35,38,41,44,47,50,53,56,59,62,65,68,71,74,77,80-HEPTACOSAOXADOOCTACONTAN-82-OL, 2-[(2',3',4'-TRIFLUOROBIPHENYL-2-YL)OXY]ETHANOL, Cathepsin S, ... | 著者 | Spraggon, G, Inagaki, H, Tsuruoka, H, Hornsby, M, Lesley, S.A, Ellman, J.A. | 登録日 | 2007-01-26 | 公開日 | 2007-05-22 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (1.6 Å) | 主引用文献 | Characterization and optimization of selective, nonpeptidic inhibitors of cathepsin S with an unprecedented binding mode. J.Med.Chem., 50, 2007
|
|
2OP4
| Crystal Structure of Quorum-Quenching Antibody 1G9 | 分子名称: | 1,2-ETHANEDIOL, Murine Antibody Fab RS2-1G9 IGG1 Heavy Chain, Murine Antibody Fab RS2-1G9 Lambda Light Chain | 著者 | Kirchdoerfer, R.N, Debler, E.W, Wilson, I.A. | 登録日 | 2007-01-26 | 公開日 | 2007-05-15 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (2.85 Å) | 主引用文献 | Crystal Structures of a Quorum-quenching Antibody. J.Mol.Biol., 368, 2007
|
|
2OP5
| |
2OP6
| Peptide-binding domain of Heat shock 70 kDa protein D precursor from C.elegans | 分子名称: | Heat shock 70 kDa protein D | 著者 | Osipiuk, J, Duggan, E, Gu, M, Voisine, C, Morimoto, R.I, Joachimiak, A, Midwest Center for Structural Genomics (MCSG) | 登録日 | 2007-01-26 | 公開日 | 2007-02-27 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (1.85 Å) | 主引用文献 | X-ray structure of peptide-binding domain of Heat shock 70 kDa protein D precursor from C.elegans To be Published
|
|
2OP7
| WW4 | 分子名称: | NEDD4-like E3 ubiquitin-protein ligase WWP1 | 著者 | Qin, H.N, Li, M.F, Pu, H, Sankaran, S, Ahmed, S, Song, J.X. | 登録日 | 2007-01-27 | 公開日 | 2007-12-11 | 最終更新日 | 2023-12-27 | 実験手法 | SOLUTION NMR | 主引用文献 | NMR structure of the forth WW domain of WWP1 To be Published
|
|
2OP8
| |
2OP9
| |
2OPA
| |
2OPB
| Structure of K57A hPNMT with inhibitor 3-fluoromethyl-7-thiomorpholinosulfonamide-THIQ and AdoHcy | 分子名称: | (3R)-3-(FLUOROMETHYL)-7-(THIOMORPHOLIN-4-YLSULFONYL)-1,2,3,4-TETRAHYDROISOQUINOLINE, PHOSPHATE ION, Phenylethanolamine N-methyltransferase, ... | 著者 | Drinkwater, N, Martin, J.L. | 登録日 | 2007-01-28 | 公開日 | 2007-10-09 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (2.8 Å) | 主引用文献 | Enzyme Adaptation to Inhibitor Binding: A Cryptic Binding Site in Phenylethanolamine N-Methyltransferase. J.Med.Chem., 50, 2007
|
|
2OPC
| Structure of Melampsora lini avirulence protein, AvrL567-A | 分子名称: | AvrL567-A, COBALT (II) ION, IMIDAZOLE | 著者 | Guncar, G, Wang, C.I, Forwood, J.K, Teh, T, Catanzariti, A.M, Ellis, J.G, Dodds, P.N, Kobe, B. | 登録日 | 2007-01-29 | 公開日 | 2007-03-06 | 最終更新日 | 2023-12-27 | 実験手法 | X-RAY DIFFRACTION (1.43 Å) | 主引用文献 | The use of Co2+ for crystallization and structure determination, using a conventional monochromatic X-ray source, of flax rust avirulence protein. Acta Crystallogr.,Sect.F, 63, 2007
|
|
2OPD
| Structure of the Neisseria meningitidis minor Type IV pilin, PilX | 分子名称: | PilX | 著者 | Dyer, D.H, Helaine, S, Pelicic, V, Forest, K.T. | 登録日 | 2007-01-29 | 公開日 | 2007-10-23 | 最終更新日 | 2024-04-03 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | 3D structure/function analysis of PilX reveals how minor pilins can modulate the virulence properties of type IV pili. Proc.Natl.Acad.Sci.Usa, 104, 2007
|
|
2OPE
| Crystal structure of the Neisseria meningitidis minor Type IV pilin, PilX, in space group P43 | 分子名称: | PilX | 著者 | Dyer, D.H, Helaine, S, Pelicic, V, Forest, K.T. | 登録日 | 2007-01-29 | 公開日 | 2007-10-23 | 最終更新日 | 2023-12-27 | 実験手法 | X-RAY DIFFRACTION (2.4 Å) | 主引用文献 | 3D structure/function analysis of PilX reveals how minor pilins can modulate the virulence properties of type IV pili. Proc.Natl.Acad.Sci.Usa, 104, 2007
|
|
2OPF
| Crystal structure of the DNA repair enzyme endonuclease-VIII (Nei) from E. coli (R252A) in complex with AP-site containing DNA substrate | 分子名称: | 5'-D(*GP*GP*CP*TP*TP*CP*AP*TP*CP*CP*TP*G)-3', 5'-D(P*CP*AP*GP*GP*AP*(PED)P*GP*AP*AP*GP*CP*C)-3', Endonuclease VIII, ... | 著者 | Golan, G, Zharov, D.O, Grollman, A.P, Shoham, G. | 登録日 | 2007-01-29 | 公開日 | 2008-02-26 | 最終更新日 | 2023-10-25 | 実験手法 | X-RAY DIFFRACTION (1.85 Å) | 主引用文献 | Active site plasticity of endonuclease VIII: Conformational changes compensating for different substrates and mutations of critical residues To be Published
|
|
2OPG
| The crystal structure of the 10th PDZ domain of MPDZ | 分子名称: | Multiple PDZ domain protein, SODIUM ION | 著者 | Gileadi, C, Phillips, C, Elkins, J, Papagrigoriou, E, Ugochukwu, E, Gorrec, F, Savitsky, P, Umeano, C, Berridge, G, Gileadi, O, Salah, E, Edwards, A, Arrowsmith, C.H, Weigelt, J, Sundstrom, M, Doyle, D.A, Structural Genomics Consortium (SGC) | 登録日 | 2007-01-29 | 公開日 | 2007-02-13 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (1.5 Å) | 主引用文献 | The crystal structure of the 10th PDZ domain of MPDZ To be Published
|
|
2OPH
| Human dipeptidyl peptidase IV in complex with an alpha amino acid inhibitor | 分子名称: | 2-acetamido-2-deoxy-alpha-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... | 著者 | Scapin, G, Weber, A.E, Duffy, J.L. | 登録日 | 2007-01-29 | 公開日 | 2007-05-08 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (2.4 Å) | 主引用文献 | 4-Aminophenylalanine and 4-aminocyclohexylalanine derivatives as potent, selective, and orally bioavailable inhibitors of dipeptidyl peptidase IV. Bioorg.Med.Chem.Lett., 17, 2007
|
|