3SH1
| Ac-AChBP ligand binding domain mutated to human alpha-7 nAChR | 分子名称: | (4R)-2-METHYLPENTANE-2,4-DIOL, (4S)-2-METHYL-2,4-PENTANEDIOL, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... | 著者 | Nemecz, A, Taylor, P.W. | 登録日 | 2011-06-15 | 公開日 | 2011-10-26 | 最終更新日 | 2023-09-13 | 実験手法 | X-RAY DIFFRACTION (2.9 Å) | 主引用文献 | Creating an alpha-7 nicotinic acetylcholine recognition domain from the
acetylcholine binding protein: crystallographic and ligand selectivity analyses J.Biol.Chem., 286, 2011
|
|
3SBX
| |
3SIO
| Ac-AChBP ligand binding domain (not including beta 9-10 linker) mutated to human alpha-7 nAChR | 分子名称: | (4R)-2-METHYLPENTANE-2,4-DIOL, (4S)-2-METHYL-2,4-PENTANEDIOL, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... | 著者 | Nemecz, A, Taylor, P.W. | 登録日 | 2011-06-19 | 公開日 | 2011-10-26 | 最終更新日 | 2024-04-03 | 実験手法 | X-RAY DIFFRACTION (2.32 Å) | 主引用文献 | Creating an alpha-7 nicotinic acetylcholine recognition domain from the
acetylcholine binding protein: crystallographic and ligand selectivity analyses J.Biol.Chem., 286, 2011
|
|
3U6Q
| MutM set 2 ApGo | 分子名称: | DNA (5'-D(*AP*GP*GP*TP*AP*GP*AP*CP*CP*TP*GP*GP*AP*CP*GP*C)-3'), DNA (5'-D(*TP*GP*CP*GP*TP*CP*CP*AP*(8OG)P*GP*TP*(CX2)P*TP*AP*CP*C)-3'), Formamidopyrimidine-DNA glycosylase, ... | 著者 | Sung, R.J, Zhang, M, Qi, Y, Verdine, G.L. | 登録日 | 2011-10-12 | 公開日 | 2012-04-25 | 最終更新日 | 2013-09-25 | 実験手法 | X-RAY DIFFRACTION (1.981 Å) | 主引用文献 | Sequence-dependent structural variation in DNA undergoing intrahelical inspection by the DNA glycosylase MutM. J.Biol.Chem., 287, 2012
|
|
2CHZ
| A pharmacological map of the PI3-K family defines a role for p110alpha in signaling: The structure of complex of phosphoinositide 3-kinase gamma with inhibitor PIK-93 | 分子名称: | N-(5-(4-CHLORO-3-(2-HYDROXY-ETHYLSULFAMOYL)- PHENYLTHIAZOLE-2-YL)-ACETAMIDE, PHOSPHATIDYLINOSITOL-4,5-BISPHOSPHATE 3-KINASE CATALYTIC SUBUNIT GAMMA ISOFORM | 著者 | Knight, Z.A, Gonzalez, B, Feldman, M.E, Zunder, E.R, Goldenberg, D.D, Williams, O, Loewith, R, Stokoe, D, Balla, A, Toth, B, Balla, T, Weiss, W.A, Williams, R.L, Shokat, K.M. | 登録日 | 2006-03-16 | 公開日 | 2006-05-22 | 最終更新日 | 2023-12-13 | 実験手法 | X-RAY DIFFRACTION (2.6 Å) | 主引用文献 | A Pharmacological Map of the Pi3-K Family Defines a Role for P110Alpha in Signaling Cell(Cambridge,Mass.), 125, 2006
|
|
2E9N
| Structure of h-CHK1 complexed with A767085 | 分子名称: | 3-(4'-HYDROXYBIPHENYL-4-YL)-N-(4-HYDROXYCYCLOHEXYL)-1,4-DIHYDROINDENO[1,2-C]PYRAZOLE-6-CARBOXAMIDE, Serine/threonine-protein kinase Chk1 | 著者 | Park, C. | 登録日 | 2007-01-26 | 公開日 | 2008-01-29 | 最終更新日 | 2024-03-13 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Discovery of 1,4-dihydroindeno[1,2-c]pyrazoles as a novel class of potent and selective checkpoint kinase 1 inhibitors. Bioorg.Med.Chem., 15, 2007
|
|
3RKF
| Crystal structure of guanine riboswitch C61U/G37A double mutant bound to thio-guanine | 分子名称: | 2-amino-1,9-dihydro-6H-purine-6-thione, COBALT HEXAMMINE(III), Guanine riboswitch | 著者 | Buck, J, Wacker, A, Warkentin, E, Woehnert, J, Wirmer-Bartoschek, J, Schwalbe, H. | 登録日 | 2011-04-18 | 公開日 | 2011-08-17 | 最終更新日 | 2023-09-13 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Influence of ground-state structure and Mg2+ binding on folding kinetics of the guanine-sensing riboswitch aptamer domain. Nucleic Acids Res., 39, 2011
|
|
3RRV
| |
3R1I
| |
3R9R
| |
3R6U
| Crystal structure of choline binding protein OpuBC from Bacillus subtilis | 分子名称: | CHOLINE ION, Choline-binding protein | 著者 | Pittelkow, M, Tschapek, B, Smits, S.H.J, Schmitt, L, Bremer, E. | 登録日 | 2011-03-22 | 公開日 | 2011-06-15 | 最終更新日 | 2023-09-13 | 実験手法 | X-RAY DIFFRACTION (1.61 Å) | 主引用文献 | The Crystal Structure of the Substrate-Binding Protein OpuBC from Bacillus subtilis in Complex with Choline. J.Mol.Biol., 411, 2011
|
|
3R20
| |
2BI8
| |
2BKV
| |
3RUR
| Staphylococcus aureus heme-bound selenomethionine-labeled IsdB-N2 | 分子名称: | Iron-regulated surface determinant protein B, MAGNESIUM ION, PROTOPORPHYRIN IX CONTAINING FE | 著者 | Gaudin, C.F.M, Grigg, J.C, Arrieta, A.L, Murphy, M.E.P. | 登録日 | 2011-05-05 | 公開日 | 2011-05-18 | 最終更新日 | 2023-12-06 | 実験手法 | X-RAY DIFFRACTION (1.7 Å) | 主引用文献 | Unique Heme-Iron Coordination by the Hemoglobin Receptor IsdB of Staphylococcus aureus. Biochemistry, 50, 2011
|
|
2BI7
| |
3RV2
| |
3RVU
| Structure of 4C1 Fab in C2221 space group | 分子名称: | 4C1 Fab - heavy chain, 4C1 Fab - light chain | 著者 | Chruszcz, M, Vailes, L.D, Chapman, M.D, Pomes, A, Minor, W. | 登録日 | 2011-05-06 | 公開日 | 2012-01-11 | 最終更新日 | 2023-09-13 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Molecular determinants for antibody binding on group 1 house dust mite allergens. J.Biol.Chem., 287, 2012
|
|
2CHB
| CHOLERA TOXIN B-PENTAMER COMPLEXED WITH GM1 PENTASACCHARIDE | 分子名称: | CHOLERA TOXIN, beta-D-galactopyranose-(1-3)-2-acetamido-2-deoxy-beta-D-galactopyranose-(1-4)-[N-acetyl-alpha-neuraminic acid-(2-3)]beta-D-galactopyranose, beta-D-galactopyranose-(1-3)-2-acetamido-2-deoxy-beta-D-galactopyranose-(1-4)-[N-acetyl-alpha-neuraminic acid-(2-3)]beta-D-galactopyranose-(1-4)-beta-D-glucopyranose | 著者 | Merritt, E.A, Hol, W.G.J. | 登録日 | 1997-06-03 | 公開日 | 1997-12-03 | 最終更新日 | 2023-08-09 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Structural studies of receptor binding by cholera toxin mutants. Protein Sci., 6, 1997
|
|
3QUH
| |
2EBF
| |
3QUA
| |
2E9O
| Structure of h-CHK1 complexed with AA582939 | 分子名称: | 4-(6-{[(4-METHYLCYCLOHEXYL)AMINO]METHYL}-1,4-DIHYDROINDENO[1,2-C]PYRAZOL-3-YL)BENZOIC ACID, Serine/threonine-protein kinase Chk1 | 著者 | Park, C. | 登録日 | 2007-01-26 | 公開日 | 2008-01-29 | 最終更新日 | 2024-03-13 | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | 主引用文献 | Discovery of 1,4-dihydroindeno[1,2-c]pyrazoles as a novel class of potent and selective checkpoint kinase 1 inhibitors. Bioorg.Med.Chem., 15, 2007
|
|
3QRE
| |
3RW9
| Crystal Structure of human Spermidine Synthase in Complex with decarboxylated S-adenosylhomocysteine | 分子名称: | 5'-S-(3-aminopropyl)-5'-thioadenosine, Spermidine synthase | 著者 | Seckute, J, McCloskey, D.E, Thomas, H.J, Secrist III, J.A, Pegg, A.E, Ealick, S.E. | 登録日 | 2011-05-08 | 公開日 | 2011-09-21 | 最終更新日 | 2024-02-28 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Binding and inhibition of human spermidine synthase by decarboxylated S-adenosylhomocysteine. Protein Sci., 20, 2011
|
|