5O8Y
| Conformational dynamism for DNA interaction in Salmonella typhimurium RcsB response regulator. | 分子名称: | 2-{2-[2-(2-{2-[2-(2-ETHOXY-ETHOXY)-ETHOXY]-ETHOXY}-ETHOXY)-ETHOXY]-ETHOXY}-ETHANOL, SULFATE ION, Transcriptional regulatory protein RcsB | 著者 | Casino, P, Marina, A, Miguel-Romero, L, Huesa, J. | 登録日 | 2017-06-14 | 公開日 | 2017-11-15 | 最終更新日 | 2024-01-17 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Conformational dynamism for DNA interaction in the Salmonella RcsB response regulator. Nucleic Acids Res., 46, 2018
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3VAQ
| Adenosine kinase from Schistosoma mansoni in complex with adenosine | 分子名称: | ADENOSINE, CHLORIDE ION, Putative adenosine kinase | 著者 | Romanello, L, Bachega, F.R, Garatt, R.C, DeMarco, R, Pereira, H.M. | 登録日 | 2011-12-29 | 公開日 | 2012-11-14 | 最終更新日 | 2023-09-13 | 実験手法 | X-RAY DIFFRACTION (2.44 Å) | 主引用文献 | Adenosine kinase from Schistosoma mansoni: structural basis for the differential incorporation of nucleoside analogues. Acta Crystallogr.,Sect.D, 69, 2013
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1PL2
| Crystal structure of human glutathione transferase (GST) A1-1 T68E mutant in complex with decarboxy-glutathione | 分子名称: | CHLORIDE ION, Glutathione S-transferase A1, N-(4-AMINOBUTANOYL)-S-(4-METHOXYBENZYL)-L-CYSTEINYLGLYCINE | 著者 | Grahn, E, Jakobsson, E, Gustafsson, A, Grehn, L, Olin, B, Wahlberg, M, Madsen, D, Kleywegt, G.J, Mannervik, B. | 登録日 | 2003-06-06 | 公開日 | 2004-06-22 | 最終更新日 | 2021-10-27 | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | 主引用文献 | New crystal structures of human glutathione transferase A1-1 shed light on glutathione binding and the conformation of the C-terminal helix. Acta Crystallogr.,Sect.D, 62, 2006
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1EDS
| SOLUTION STRUCTURE OF INTRADISKAL LOOP 1 OF BOVINE RHODOPSIN (RHODOPSIN RESIDUES 92-123) | 分子名称: | RHODOPSIN | 著者 | Yeagle, P.L, Salloum, A, Chopra, A, Bhawsar, N, Ali, L. | 登録日 | 2000-01-28 | 公開日 | 2000-08-09 | 最終更新日 | 2024-05-22 | 実験手法 | SOLUTION NMR | 主引用文献 | Structures of the intradiskal loops and amino terminus of the G-protein receptor, rhodopsin. J.Pept.Res., 55, 2000
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5OA1
| RNA polymerase I pre-initiation complex | 分子名称: | ALA-ALA-ALA-ALA-ALA-ALA-ALA-ALA-ALA, ALA-ALA-ALA-ALA-ALA-ALA-ALA-ALA-ALA-ALA, ALA-ALA-ALA-ALA-ALA-ALA-ALA-ALA-ALA-ALA-ALA-ALA, ... | 著者 | Sadian, Y, Tafur, L, Kosinski, J, Jakobi, A.J, Muller, C.W. | 登録日 | 2017-06-20 | 公開日 | 2017-07-26 | 最終更新日 | 2018-10-24 | 実験手法 | ELECTRON MICROSCOPY (4.4 Å) | 主引用文献 | Structural insights into transcription initiation by yeast RNA polymerase I. EMBO J., 36, 2017
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5ZXD
| Crystal structure of ATP-bound human ABCF1 | 分子名称: | ADENOSINE-5'-TRIPHOSPHATE, ATP-binding cassette sub-family F member 1 | 著者 | Qu, L, Jiang, Y, Liu, Z.J. | 登録日 | 2018-05-18 | 公開日 | 2018-07-25 | 最終更新日 | 2018-09-19 | 実験手法 | X-RAY DIFFRACTION (2.288 Å) | 主引用文献 | Crystal Structure of ATP-Bound Human ABCF1 Demonstrates a Unique Conformation of ABC Proteins Structure, 26, 2018
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5O1J
| Lytic transglycosylase in action | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-1,6-anhydro-N-acetyl-beta-D-glucopyranosamine, Putative soluble lytic murein transglycosylase, ZINC ION | 著者 | Williams, A.H, Rateau, L, Hoauz, A, Boneca, I.G. | 登録日 | 2017-05-18 | 公開日 | 2018-03-14 | 最終更新日 | 2024-01-17 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | A step-by-stepin crystalloguide to bond cleavage and 1,6-anhydro-sugar product synthesis by a peptidoglycan-degrading lytic transglycosylase. J. Biol. Chem., 293, 2018
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4CFG
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1Q0S
| Binary Structure of T4DAM with AdoHcy | 分子名称: | DNA adenine methylase, S-ADENOSYL-L-HOMOCYSTEINE | 著者 | Yang, Z, Horton, J.R, Zhou, L, Zhang, X.J, Dong, A, Zhang, X, Schlagman, S.L, Kossykh, V, Hattman, S, Cheng, X. | 登録日 | 2003-07-17 | 公開日 | 2003-09-23 | 最終更新日 | 2024-02-14 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Structure of the bacteriophage T4 DNA adenine methyltransferase Nat.Struct.Biol., 10, 2003
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1PQY
| Crystal structure of formyl-coA transferase yfdW from E. coli | 分子名称: | Hypothetical protein yfdW | 著者 | Gogos, A, Gorman, J, Shapiro, L, Burley, S.K, New York SGX Research Center for Structural Genomics (NYSGXRC) | 登録日 | 2003-06-19 | 公開日 | 2003-09-30 | 最終更新日 | 2024-10-30 | 実験手法 | X-RAY DIFFRACTION (2.35 Å) | 主引用文献 | Structure of Escherichia coli YfdW, a type III CoA transferase. Acta Crystallogr.,Sect.D, 60, 2004
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4C03
| Crystal structure of M. musculus protein arginine methyltransferase PRMT6 reduced | 分子名称: | PROTEIN ARGININE N-METHYLTRANSFERASE 6, SINEFUNGIN | 著者 | Bonnefond, L, Cura, V, Troffer-Charlier, N, Mailliot, J, Wurtz, J.M, Cavarelli, J. | 登録日 | 2013-07-31 | 公開日 | 2014-07-30 | 最終更新日 | 2023-12-20 | 実験手法 | X-RAY DIFFRACTION (1.58 Å) | 主引用文献 | Functional Insights from High Resolution Structures of Mouse Protein Arginine Methyltransferase 6. J.Struct.Biol., 191, 2015
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1Q2U
| Crystal structure of DJ-1/RS and implication on familial Parkinson's disease | 分子名称: | RNA-binding protein regulatory subunit | 著者 | Huai, Q, Sun, Y, Wang, H, Chin, L.S, Li, L, Robinson, H, Ke, H. | 登録日 | 2003-07-26 | 公開日 | 2003-10-07 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (1.6 Å) | 主引用文献 | Crystal structure of DJ-1/RS and implication on familial Parkinson's disease Febs Lett., 549, 2003
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8WM3
| Cryo-EM structure of ACE2-SIT1 complex with tiagabine | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, Angiotensin-converting enzyme 2, ... | 著者 | Yan, R, Hu, Z, Dai, L, Zhang, T. | 登録日 | 2023-10-02 | 公開日 | 2024-09-25 | 実験手法 | ELECTRON MICROSCOPY (3.34 Å) | 主引用文献 | Cryo-EM structure of ACE2-SIT1 in complex with tiagabine. J.Biol.Chem., 300, 2024
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5O62
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8WJB
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1EET
| HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH THE INHIBITOR MSC204 | 分子名称: | 1-(5-BROMO-PYRIDIN-2-YL)-3-[2-(6-FLUORO-2-HYDROXY-3-PROPIONYL-PHENYL)-CYCLOPROPYL]-UREA, HIV-1 REVERSE TRANSCRIPTASE | 著者 | Hogberg, M, Sahlberg, C, Engelhardt, P, Noreen, R, Kangasmetsa, J, Johansson, N.G, Oberg, B, Vrang, L, Zhang, H, Sahlberg, B.L, Unge, T, Lovgren, S, Fridborg, K, Backbro, K. | 登録日 | 2000-02-03 | 公開日 | 2001-02-07 | 最終更新日 | 2024-02-07 | 実験手法 | X-RAY DIFFRACTION (2.73 Å) | 主引用文献 | Urea-PETT compounds as a new class of HIV-1 reverse transcriptase inhibitors. 3. Synthesis and further structure-activity relationship studies of PETT analogues. J.Med.Chem., 42, 1999
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5O6S
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1EFK
| STRUCTURE OF HUMAN MALIC ENZYME IN COMPLEX WITH KETOMALONATE | 分子名称: | ALPHA-KETOMALONIC ACID, MAGNESIUM ION, MALIC ENZYME, ... | 著者 | Yang, Z, Floyd, D.L, Loeber, G, Tong, L. | 登録日 | 2000-02-09 | 公開日 | 2000-03-08 | 最終更新日 | 2011-07-13 | 実験手法 | X-RAY DIFFRACTION (2.6 Å) | 主引用文献 | Structure of a closed form of human malic enzyme and implications for catalytic mechanism. Nat.Struct.Biol., 7, 2000
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3VJ6
| Structure of the MHC class Ib molecule Qa-1b | 分子名称: | Beta-2-microglobulin, H-2 class I histocompatibility antigen, D-37 alpha chain, ... | 著者 | Zeng, L, Clements, C.S, Rossjohn, J. | 登録日 | 2011-10-12 | 公開日 | 2012-03-14 | 最終更新日 | 2024-10-30 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | A structural basis for antigen presentation by the MHC class Ib molecule, Qa-1b J.Immunol., 188, 2012
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5O75
| Ube4B U-box domain | 分子名称: | SULFATE ION, Ubiquitin conjugation factor E4 B | 著者 | Gabrielsen, M, Buetow, L, Nakasone, M.A, Huang, D.T. | 登録日 | 2017-06-08 | 公開日 | 2017-11-01 | 最終更新日 | 2024-01-17 | 実験手法 | X-RAY DIFFRACTION (1.483 Å) | 主引用文献 | A General Strategy for Discovery of Inhibitors and Activators of RING and U-box E3 Ligases with Ubiquitin Variants. Mol. Cell, 68, 2017
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8WJW
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4BTY
| Crystal structure of human vascular adhesion protein-1 in complex with pyridazinone inhibitors | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 5-[4-(4-methylpiperazin-1-yl)phenylamino]-2-(4-chlorophenyl)-6-(1H-1,2,4-triazol-5-yl)-3(2H)-pyridazinone, ... | 著者 | Bligt-Linden, E, Pihlavisto, M, Szatmari, I, Otwinowski, Z, Smith, D.J, Lazar, L, Fulop, F, Salminen, T.A. | 登録日 | 2013-06-19 | 公開日 | 2013-12-18 | 最終更新日 | 2023-12-20 | 実験手法 | X-RAY DIFFRACTION (3.1 Å) | 主引用文献 | Novel Pyridazinone Inhibitors for Vascular Adhesion Protein- 1 (Vap-1): Old Target - New Inhibition Mode. J.Med.Chem., 56, 2013
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8WK9
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4C37
| PKA-S6K1 Chimera with compound 21a (CCT196539) bound | 分子名称: | (4S)-2-METHYL-2,4-PENTANEDIOL, 4-(6-bromo-1-ethyl-1H-imidazo[4,5-c]pyridin-2-yl)-1,2,5-oxadiazol-3-amine, CAMP-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT ALPHA, ... | 著者 | Couty, S, Westwood, I.M, Kalusa, A, Cano, C, Travers, J, Boxall, K, Chow, C.L, Burns, S, Schmitt, J, Pickard, L, Barillari, C, McAndrew, P.C, Clarke, P.A, Linardopoulos, S, Griffin, R.J, Aherne, G.W, Raynaud, F.I, Workman, P, Jones, K, van Montfort, R.L.M. | 登録日 | 2013-08-21 | 公開日 | 2013-10-09 | 最終更新日 | 2024-10-09 | 実験手法 | X-RAY DIFFRACTION (1.7 Å) | 主引用文献 | The discovery of potent ribosomal S6 kinase inhibitors by high-throughput screening and structure-guided drug design. Oncotarget, 4, 2013
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8WK5
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