PDB: 45176 resultsInfo pagesStatus searchChemie searchBIRD

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4AQT	Laminin gamma1 LN-LE1-2 structure Descriptor: 2-acetamido-2-deoxy-beta-D-glucopyranose, CALCIUM ION, LAMININ SUBUNIT GAMMA-1, ... Authors: Carafoli, F, Hussain, S, Hohenester, E. Deposit date: 2012-04-19 Release date: 2012-08-15 Last modified: 2023-12-20 Method: X-RAY DIFFRACTION (3.2 Å) Cite: Crystal Structures of the Network-Forming Short-Arm Tips of the Laminin Beta1 and Gamma1 Chains. Plos One, 7, 2012
421D	5'-D(*TP*TP*CP*TP*TP*(BRO)CP*TP*TP*C)-3', 5'-R(*GP*AP*AP*GP*AP*AP*GP*AP*A)-3' Descriptor: DNA (5'-D(*TP*TP*CP*TP*TP*(CBR)P*TP*TP*C)-3'), RNA (5'-R(*GP*AP*AP*GP*AP*AP*GP*AP*A)-3') Authors: Xiong, Y, Sundaralingam, M. Deposit date: 1998-08-16 Release date: 1999-01-05 Last modified: 2023-12-27 Method: X-RAY DIFFRACTION (1.8 Å) Cite: Crystal structure and conformation of a DNA-RNA hybrid duplex with a polypurine RNA strand: d(TTCTTBr5CTTC)-r(GAAGAAGAA). Structure, 6, 1998
3QTZ	CDK2 in complex with inhibitor RC-2-36 Descriptor: 1,2-ETHANEDIOL, 4-{[4-amino-5-(3-fluorobenzoyl)-1,3-thiazol-2-yl]amino}benzenesulfonamide, Cyclin-dependent kinase 2 Authors: Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. Deposit date: 2011-02-23 Release date: 2012-10-31 Last modified: 2023-09-13 Method: X-RAY DIFFRACTION (2 Å) Cite: Development of highly potent and selective diaminothiazole inhibitors of cyclin-dependent kinases. J.Med.Chem., 56, 2013
3QZG	CDK2 in complex with inhibitor JWS-6-76 Descriptor: 1,2-ETHANEDIOL, 2-(4,6-diamino-1,3,5-triazin-2-yl)-4-fluorophenol, Cyclin-dependent kinase 2 Authors: Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. Deposit date: 2011-03-06 Release date: 2012-08-08 Last modified: 2023-09-13 Method: X-RAY DIFFRACTION (1.75 Å) Cite: Structure-guided optimization of novel CDK2 inhibitors discovered by high-throughput screening To be Published
3MPG	Dihydroorotase from Bacillus anthracis Descriptor: Dihydroorotase, ZINC ION Authors: Santarsiero, B.D, Mehboob, S, Johnson, M.E. Deposit date: 2010-04-26 Release date: 2010-11-10 Last modified: 2024-02-21 Method: X-RAY DIFFRACTION (2.6 Å) Cite: Structure of dihydroorotase from Bacillus anthracis at 2.6A resolution. Acta Crystallogr.,Sect.F, 66, 2010
3MQS	Crystal Structure of the USP7:Hdm2(PSTS) complex Descriptor: Hdm2 peptide, Ubiquitin carboxyl-terminal hydrolase 7 Authors: Saridakis, V. Deposit date: 2010-04-28 Release date: 2010-08-25 Last modified: 2023-09-06 Method: X-RAY DIFFRACTION (2.4 Å) Cite: Crystal Structure of USP7 To be Published
414D	5'-D(*GP*GP*GP*GP*CP*GP*CP*CP*CP*C)-3' Descriptor: DNA (5'-D(*GP*GP*GP*GP*CP*GP*CP*CP*CP*C)-3') Authors: Savitha, G, Viswamitra, M.A. Deposit date: 1998-07-13 Release date: 1999-06-14 Last modified: 2024-02-28 Method: X-RAY DIFFRACTION (1.9 Å) Cite: An A-DNA structure with two independent duplexes in the asymmetric unit. Acta Crystallogr.,Sect.D, 55, 1999
428D	STRUCTURE OF THE POTASSIUM FORM OF CGCGAATTCGCG: DNA DEFORMATION BY ELECTROSTATIC COLLAPSE AROUND SMALL CATIONS Descriptor: DNA (5'-D(*CP*GP*CP*GP*AP*AP*TP*TP*CP*GP*CP*G)-3'), MAGNESIUM ION, SPERMINE Authors: Shui, X, Sines, C.C, McFail-Isom, L, VanDerveer, D, Williams, L.D. Deposit date: 1998-09-28 Release date: 1998-10-09 Last modified: 2024-04-03 Method: X-RAY DIFFRACTION (1.75 Å) Cite: Structure of the potassium form of CGCGAATTCGCG: DNA deformation by electrostatic collapse around inorganic cations. Biochemistry, 37, 1998
3QRU	CDK2 in complex with inhibitor NSK-MC1-12 Descriptor: (5S)-N-methyl-5-(2-methylbutan-2-yl)-4,5,6,7-tetrahydro-2H-indazole-3-carboxamide, 1,2-ETHANEDIOL, Cyclin-dependent kinase 2 Authors: Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. Deposit date: 2011-02-18 Release date: 2012-08-08 Last modified: 2023-09-13 Method: X-RAY DIFFRACTION (1.95 Å) Cite: Structure-guided optimization of novel CDK2 inhibitors discovered by high-throughput screening To be Published
3QTQ	CDK2 in complex with inhibitor RC-1-137 Descriptor: 1,2-ETHANEDIOL, Cyclin-dependent kinase 2, [4-amino-2-(prop-2-en-1-ylamino)-1,3-thiazol-5-yl](pyridin-3-yl)methanone Authors: Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. Deposit date: 2011-02-23 Release date: 2012-10-31 Last modified: 2023-09-13 Method: X-RAY DIFFRACTION (1.8 Å) Cite: Development of highly potent and selective diaminothiazole inhibitors of cyclin-dependent kinases. J.Med.Chem., 56, 2013
3QTW	CDK2 in complex with inhibitor RC-2-13 Descriptor: 1,2-ETHANEDIOL, Cyclin-dependent kinase 2, [4-amino-2-(phenylamino)-1,3-thiazol-5-yl](pyridin-3-yl)methanone Authors: Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. Deposit date: 2011-02-23 Release date: 2012-10-31 Last modified: 2023-09-13 Method: X-RAY DIFFRACTION (1.85 Å) Cite: Development of highly potent and selective diaminothiazole inhibitors of cyclin-dependent kinases. J.Med.Chem., 56, 2013
445D	5'-D(*CP*GP*CP*GP*AP*AP*TP*TP*CP*GP*CP*G)-3', Benzimidazole derivative complex Descriptor: 2'-(3-IODOPHENYL)-5-(4-METHYL-1-PIPERAZINYL)-2,5'-BI-BENZIMIDAZOLE, DNA (5'-D(*CP*GP*CP*GP*AP*AP*TP*TP*CP*GP*CP*G)-3') Authors: Squire, C.J, Baker, L.J, Clark, G.R, Martin, R.F, White, J. Deposit date: 1999-01-14 Release date: 2000-02-02 Last modified: 2023-12-27 Method: X-RAY DIFFRACTION (2.6 Å) Cite: Structures of m-iodo Hoechst-DNA complexes in crystals with reduced solvent content: implications for minor groove binder drug design. Nucleic Acids Res., 28, 2000
456D	MOLECULAR AND CRYSTAL STRUCTURE OF D(CGCGMO6AATCCGCG): THE WATSON-CRICK TYPE N6-METHOXYADENOSINE/CYTIDINE BASE-PAIRS IN B-DNA Descriptor: DNA (5'-D(*CP*GP*CP*GP*(A47)P*AP*TP*CP*CP*GP*CP*G)-3'), MAGNESIUM ION Authors: Chatake, T, Ono, A, Ueno, Y, Matsuda, A, Takenaka, A. Deposit date: 1999-03-06 Release date: 2000-01-01 Last modified: 2023-12-27 Method: X-RAY DIFFRACTION (1.6 Å) Cite: Crystallographic studies on damaged DNAs. I. An N(6)-methoxyadenine residue forms a Watson-Crick pair with a cytosine residue in a B-DNA duplex. J.Mol.Biol., 294, 1999
3QTU	CDK2 in complex with inhibitor RC-2-132 Descriptor: 4-{[4-amino-5-(4-sulfamoylbenzoyl)-1,3-thiazol-2-yl]amino}benzenesulfonamide, Cyclin-dependent kinase 2 Authors: Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. Deposit date: 2011-02-23 Release date: 2012-10-31 Last modified: 2023-09-13 Method: X-RAY DIFFRACTION (1.82 Å) Cite: Development of highly potent and selective diaminothiazole inhibitors of cyclin-dependent kinases. J.Med.Chem., 56, 2013
424D	5'-D(*AP*CP*CP*GP*AP*CP*GP*TP*CP*GP*GP*T)-3' Descriptor: DNA (5'-D(*AP*CP*CP*GP*AP*CP*GP*TP*CP*GP*GP*T)-3') Authors: Rozenberg, H, Rabinovich, D, Frolow, F, Hegde, R.S, Shakked, Z. Deposit date: 1998-09-14 Release date: 1999-10-14 Last modified: 2024-04-03 Method: X-RAY DIFFRACTION (2.7 Å) Cite: Structural code for DNA recognition revealed in crystal structures of papillomavirus E2-DNA targets. Proc.Natl.Acad.Sci.USA, 95, 1998
43C9	CRYSTALLOGRAPHIC STRUCTURE OF THE ESTEROLYTIC AND AMIDOLYTIC 43C9 ANTIBODY Descriptor: PROTEIN (IMMUNOGLOBULIN (HEAVY CHAIN)), PROTEIN (IMMUNOGLOBULIN (LIGHT CHAIN)) Authors: Thayer, M.M, Getzoff, E.D, Roberts, V.A. Deposit date: 1999-03-10 Release date: 1999-08-18 Last modified: 2023-12-27 Method: X-RAY DIFFRACTION (2.2 Å) Cite: Structural basis for amide hydrolysis catalyzed by the 43C9 antibody. J.Mol.Biol., 291, 1999
478D	CRYSTAL STRUCTURE OF THE B-DNA DODECAMER 5'-D(CGCGAA(TAF)TCGCG), WHERE TAF IS 2'-DEOXY-2'-FLUORO-ARABINO-FURANOSYL THYMINE Descriptor: 5'-D(*CP*GP*CP*GP*AP*AP*(TAF)P*TP*CP*GP*CP*G)-3', CALCIUM ION Authors: Minasov, G, Tereshko, V, Egli, M. Deposit date: 1999-06-26 Release date: 1999-07-19 Last modified: 2024-02-28 Method: X-RAY DIFFRACTION (2.2 Å) Cite: Atomic-resolution crystal structures of B-DNA reveal specific influences of divalent metal ions on conformation and packing. J.Mol.Biol., 291, 1999
4AOP	SULFITE REDUCTASE HEMOPROTEIN PARTIALLY PHOTOREDUCED WITH PROFLAVINE EDTA, PHOSPHATE PARTIALLY BOUND Descriptor: IRON/SULFUR CLUSTER, PHOSPHATE ION, POTASSIUM ION, ... Authors: Crane, B.R, Getzoff, E.D. Deposit date: 1997-07-09 Release date: 1998-01-14 Last modified: 2023-12-27 Method: X-RAY DIFFRACTION (1.8 Å) Cite: Structures of the siroheme- and Fe4S4-containing active center of sulfite reductase in different states of oxidation: heme activation via reduction-gated exogenous ligand exchange. Biochemistry, 36, 1997
3MKQ	Crystal structure of yeast alpha/betaprime-COP subcomplex of the COPI vesicular coat Descriptor: Coatomer beta'-subunit, Coatomer subunit alpha Authors: Lee, C, Goldberg, J. Deposit date: 2010-04-15 Release date: 2010-07-14 Last modified: 2024-02-21 Method: X-RAY DIFFRACTION (2.5 Å) Cite: Structure of coatomer cage proteins and the relationship among COPI, COPII, and clathrin vesicle coats. Cell(Cambridge,Mass.), 142, 2010
3QRT	CDK2 in complex with inhibitor NSK-MC2-55 Descriptor: (5R)-5-(2-methylbutan-2-yl)-N-(4-sulfamoylbenzyl)-4,5,6,7-tetrahydro-2H-indazole-3-carboxamide, 1,2-ETHANEDIOL, Cyclin-dependent kinase 2 Authors: Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. Deposit date: 2011-02-18 Release date: 2012-08-08 Last modified: 2023-09-13 Method: X-RAY DIFFRACTION (1.75 Å) Cite: Structure-guided optimization of novel CDK2 inhibitors discovered by high-throughput screening To be Published
439D	5'-R(*CP*UP*GP*GP*GP*CP*GP*G)-3', 5'-R(*CP*CP*GP*CP*CP*UP*GP*G)-3' Descriptor: BARIUM ION, RNA (5'-R(*CP*CP*GP*CP*CP*UP*GP*G)-3'), RNA (5'-R(*CP*UP*GP*GP*GP*CP*GP*G)-3') Authors: Perbandt, M, Lorenz, S, Vallazza, M, Erdmann, V.A, Betzel, C. Deposit date: 1999-01-05 Release date: 2001-09-14 Last modified: 2023-12-27 Method: X-RAY DIFFRACTION (1.6 Å) Cite: Structure of an RNA duplex with an unusual G.C pair in wobble-like conformation at 1.6 A resolution. Acta Crystallogr.,Sect.D, 57, 2001
448D	5'-D(*CP*GP*CP*GP*AP*AP*TP*TP*CP*GP*CP*G)-3', BENZIMIDAZOLE DERIVATIVE COMPLEX Descriptor: 2'-(3-IODO-4-METHOXYPHENYL)-5-(4-METHYL-1-PIPERAZINYL)-2,5'-BI-BENZIMIDAZOLE, DNA (5'-D(*CP*GP*CP*GP*AP*AP*TP*TP*CP*GP*CP*G)-3') Authors: Clark, G.R, Squire, C.J, Martin, R.F, White, J. Deposit date: 1999-01-20 Release date: 2000-02-02 Last modified: 2023-12-27 Method: X-RAY DIFFRACTION (2.2 Å) Cite: Structures of m-iodo Hoechst-DNA complexes in crystals with reduced solvent content: implications for minor groove binder drug design. Nucleic Acids Res., 28, 2000
3MAV	Crystal structure of Plasmodium vivax putative farnesyl pyrophosphate synthase (Pv092040) Descriptor: Farnesyl pyrophosphate synthase, SULFATE ION Authors: Dong, A, Dunford, J, Lew, J, Wernimont, A.K, Ren, H, Zhao, Y, Koeieradzki, I, Opperman, U, Sundstrom, M, Weigelt, J, Edwards, A.M, Arrowsmith, C.H, Bochkarev, A, Hui, R, Artz, J.D, Structural Genomics Consortium (SGC) Deposit date: 2010-03-24 Release date: 2010-04-14 Last modified: 2023-09-06 Method: X-RAY DIFFRACTION (2.1 Å) Cite: Molecular characterization of a novel geranylgeranyl pyrophosphate synthase from Plasmodium parasites. J.Biol.Chem., 286, 2011
3QTR	CDK2 in complex with inhibitor RC-1-148 Descriptor: Cyclin-dependent kinase 2, [4-amino-2-(phenylamino)-1,3-thiazol-5-yl](phenyl)methanone Authors: Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. Deposit date: 2011-02-23 Release date: 2012-10-31 Last modified: 2023-09-13 Method: X-RAY DIFFRACTION (1.85 Å) Cite: Development of highly potent and selective diaminothiazole inhibitors of cyclin-dependent kinases. J.Med.Chem., 56, 2013
3QQH	CDK2 in complex with inhibitor L2-2 Descriptor: 1,2-ETHANEDIOL, 2-[4-amino-6-(phenylamino)-1,3,5-triazin-2-yl]-4-chlorophenol, Cyclin-dependent kinase 2, ... Authors: Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. Deposit date: 2011-02-15 Release date: 2012-08-08 Last modified: 2023-09-13 Method: X-RAY DIFFRACTION (1.87 Å) Cite: Structure-guided optimization of novel CDK2 inhibitors discovered by high-throughput screening To be Published

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