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1C58	CRYSTAL STRUCTURE OF CYCLOAMYLOSE 26 Descriptor: Cyclohexacosakis-(1-4)-(alpha-D-glucopyranose) Authors: Gessler, K, Saenger, W, Nimz, O. Deposit date: 1999-11-04 Release date: 1999-11-10 Last modified: 2024-04-03 Method: X-RAY DIFFRACTION (0.99 Å) Cite: V-Amylose at atomic resolution: X-ray structure of a cycloamylose with 26 glucose residues (cyclomaltohexaicosaose). Proc.Natl.Acad.Sci.USA, 96, 1999
1C9B	CRYSTAL STRUCTURE OF A HUMAN TBP CORE DOMAIN-HUMAN TFIIB CORE DOMAIN COMPLEX BOUND TO AN EXTENDED, MODIFIED ADENOVIRAL MAJOR LATE PROMOTER (ADMLP) Descriptor: ADMLP TATA-BOX DNA CONTAINING IIB RECOGNITION ELEMENT, GENERAL TRANSCRIPTION FACTOR IIB, TATA BOX BINDING PROTEIN Authors: Tsai, F.T.F, Sigler, P.B. Deposit date: 1999-08-01 Release date: 2000-01-10 Last modified: 2024-02-07 Method: X-RAY DIFFRACTION (2.65 Å) Cite: Structural basis of preinitiation complex assembly on human pol II promoters. EMBO J., 19, 2000
1BRN	SUBSITE BINDING IN AN RNASE: STRUCTURE OF A BARNASE-TETRANUCLEOTIDE COMPLEX AT 1.76 ANGSTROMS RESOLUTION Descriptor: DNA (5'-D(*CP*GP*AP*C)-3'), PROTEIN (BARNASE (E.C.3.1.27.-)) Authors: Buckle, A.M, Fersht, A.R. Deposit date: 1993-11-17 Release date: 1994-01-31 Last modified: 2024-02-07 Method: X-RAY DIFFRACTION (1.76 Å) Cite: Subsite binding in an RNase: structure of a barnase-tetranucleotide complex at 1.76-A resolution. Biochemistry, 33, 1994
1C4D	GRAMICIDIN CSCL COMPLEX Descriptor: CESIUM ION, CHLORIDE ION, GRAMICIDIN A, ... Authors: Wallace, B.A. Deposit date: 1999-06-04 Release date: 2000-01-03 Last modified: 2023-11-15 Method: X-RAY DIFFRACTION (2 Å) Cite: The Gramicidin Pore: Crystal Structure of a Cesium Complex. Science, 241, 1988
1C2W	23S RRNA STRUCTURE FITTED TO A CRYO-ELECTRON MICROSCOPIC MAP AT 7.5 ANGSTROMS RESOLUTION Descriptor: 23S RIBOSOMAL RNA Authors: Brimacombe, R, Mueller, F. Deposit date: 1999-07-28 Release date: 2000-04-10 Last modified: 2023-12-27 Method: ELECTRON MICROSCOPY (7.5 Å) Cite: The 3D arrangement of the 23 S and 5 S rRNA in the Escherichia coli 50 S ribosomal subunit based on a cryo-electron microscopic reconstruction at 7.5 A resolution. J.Mol.Biol., 298, 2000
1C51	PHOTOSYNTHETIC REACTION CENTER AND CORE ANTENNA SYSTEM (TRIMERIC), ALPHA CARBON ONLY Descriptor: CHLOROPHYLL A, IRON/SULFUR CLUSTER, PHYLLOQUINONE, ... Authors: Klukas, O, Schubert, W.D, Jordan, P, Krauss, N, Fromme, P, Witt, H.T, Saenger, W. Deposit date: 1999-10-21 Release date: 2000-03-31 Last modified: 2023-12-27 Method: X-RAY DIFFRACTION (4 Å) Cite: Photosystem I, an improved model of the stromal subunits PsaC, PsaD, and PsaE. J.Biol.Chem., 274, 1999
1C4W	1.9 A STRUCTURE OF A-THIOPHOSPHONATE MODIFIED CHEY D57C Descriptor: CHEMOTAXIS PROTEIN CHEY Authors: Halkides, C.J, McEvoy, M.M, Matsumura, P, Volz, K, Dahlquist, F.W. Deposit date: 1999-09-28 Release date: 2000-05-08 Last modified: 2023-12-27 Method: X-RAY DIFFRACTION (1.84 Å) Cite: The 1.9 A resolution crystal structure of phosphono-CheY, an analogue of the active form of the response regulator, CheY. Biochemistry, 39, 2000
1CDC	CD2, N-TERMINAL DOMAIN (1-99), TRUNCATED FORM Descriptor: CD2 Authors: Murray, A.J, Barclay, A.N, Brady, R.L. Deposit date: 1995-05-23 Release date: 1995-09-15 Last modified: 2024-02-07 Method: X-RAY DIFFRACTION (2 Å) Cite: One sequence, two folds: a metastable structure of CD2. Proc.Natl.Acad.Sci.USA, 92, 1995
1AYV	CRYSTAL STRUCTURE OF CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT THIAZOLHYDRAZIDE INHIBITOR Descriptor: CATHEPSIN K, N-[2-[1-(N-BENZYLOXYCARBONYLAMINO)-3-METHYLBUTYL]THIAZOL-4-YLCARBONYL]-N'-(BENZYLOXYCARBONYL-L-LEUCINYL)HYDRAZIDE Authors: Zhao, B, Smith, W.W, Janson, C.A, Abdel-Meguid, S.S. Deposit date: 1997-11-10 Release date: 1998-11-25 Last modified: 2023-08-02 Method: X-RAY DIFFRACTION (2.3 Å) Cite: Design of potent and selective human cathepsin K inhibitors that span the active site. Proc.Natl.Acad.Sci.USA, 94, 1997
1B13	CLOSTRIDIUM PASTEURIANUM RUBREDOXIN G10A MUTANT Descriptor: FE (III) ION, PROTEIN (RUBREDOXIN) Authors: Maher, M.J, Guss, J.M, Wilce, M.C.J, Wedd, A.G. Deposit date: 1998-11-26 Release date: 1999-05-27 Last modified: 2023-08-09 Method: X-RAY DIFFRACTION (1.5 Å) Cite: Rubredoxin from Clostridium pasteurianum. Structures of G10A, G43A and G10VG43A mutant proteins. Mutation of conserved glycine 10 to valine causes the 9-10 peptide link to invert. Acta Crystallogr.,Sect.D, 55, 1999
1AYU	CRYSTAL STRUCTURE OF CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT SYMMETRIC BISCARBOHYDRAZIDE INHIBITOR Descriptor: 1,5-BIS(N-BENZYLOXYCARBONYL-L-LEUCINYL)CARBOHYDRAZIDE, CATHEPSIN K Authors: Zhao, B, Smith, W.W, Janson, C.A, Abdel-Meguid, S.S. Deposit date: 1997-11-10 Release date: 1998-11-25 Last modified: 2023-08-02 Method: X-RAY DIFFRACTION (2.2 Å) Cite: Design of potent and selective human cathepsin K inhibitors that span the active site. Proc.Natl.Acad.Sci.USA, 94, 1997
1B2O	CLOSTRIDIUM PASTEURIANUM RUBREDOXIN G10VG43A MUTANT Descriptor: FE (III) ION, PROTEIN (RUBREDOXIN) Authors: Maher, M.J, Guss, J.M, Wilce, M.C.J, Wedd, A.G. Deposit date: 1998-11-30 Release date: 1999-05-27 Last modified: 2023-08-09 Method: X-RAY DIFFRACTION (1.9 Å) Cite: Rubredoxin from Clostridium pasteurianum. Structures of G10A, G43A and G10VG43A mutant proteins. Mutation of conserved glycine 10 to valine causes the 9-10 peptide link to invert. Acta Crystallogr.,Sect.D, 55, 1999
1B2J	CLOSTRIDIUM PASTEURIANUM RUBREDOXIN G43A MUTANT Descriptor: FE (III) ION, PROTEIN (RUBREDOXIN) Authors: Maher, M.J, Guss, J.M, Wilce, M.C.J, Wedd, A.G. Deposit date: 1998-11-27 Release date: 1999-05-27 Last modified: 2023-08-09 Method: X-RAY DIFFRACTION (1.6 Å) Cite: Rubredoxin from Clostridium pasteurianum. Structures of G10A, G43A and G10VG43A mutant proteins. Mutation of conserved glycine 10 to valine causes the 9-10 peptide link to invert. Acta Crystallogr.,Sect.D, 55, 1999
1APW	CRYSTALLOGRAPHIC ANALYSIS OF TRANSITION STATE MIMICS BOUND TO PENICILLOPEPSIN: DIFLUOROSTATINE-AND DIFLUOROSTATONE-CONTAINING PEPTIDES Descriptor: DIMETHYLFORMAMIDE, INHIBITOR ISOVALERYL (IVA)-VAL-VAL-DIFLUOROSTATINE-N-METHYLAMINE, PENICILLOPEPSIN, ... Authors: Sielecki, A.R, James, M.N.G. Deposit date: 1991-12-16 Release date: 1994-01-31 Last modified: 2020-07-29 Method: X-RAY DIFFRACTION (1.8 Å) Cite: Crystallographic analysis of transition state mimics bound to penicillopepsin: difluorostatine- and difluorostatone-containing peptides. Biochemistry, 31, 1992
1CI6	TRANSCRIPTION FACTOR ATF4-C/EBP BETA BZIP HETERODIMER Descriptor: BETA-MERCAPTOETHANOL, FE (III) ION, TRANSCRIPTION FACTOR ATF-4, ... Authors: Podust, L.M, Kim, Y. Deposit date: 1999-04-07 Release date: 2000-12-04 Last modified: 2023-08-09 Method: X-RAY DIFFRACTION (2.6 Å) Cite: Crystal structure of the CCAAT box/enhancer-binding protein beta activating transcription factor-4 basic leucine zipper heterodimer in the absence of DNA J.Biol.Chem., 276, 2001
1AAL	STRUCTURAL EFFECTS INDUCED BY MUTAGENESIS AFFECTED BY CRYSTAL PACKING FACTORS: THE STRUCTURE OF A 30-51 DISULFIDE MUTANT OF BASIC PANCREATIC TRYPSIN INHIBITOR Descriptor: BOVINE PANCREATIC TRYPSIN INHIBITOR, PHOSPHATE ION Authors: Eigenbrot, C, Randal, M, Kossiakoff, A.A. Deposit date: 1992-04-09 Release date: 1993-10-31 Last modified: 2017-11-29 Method: X-RAY DIFFRACTION (1.6 Å) Cite: Structural effects induced by mutagenesis affected by crystal packing factors: the structure of a 30-51 disulfide mutant of basic pancreatic trypsin inhibitor. Proteins, 14, 1992
1AGP	THREE-DIMENSIONAL STRUCTURES AND PROPERTIES OF A TRANSFORMING AND A NONTRANSFORMING GLY-12 MUTANT OF P21-H-RAS Descriptor: C-H-RAS P21 PROTEIN, MAGNESIUM ION, PHOSPHOAMINOPHOSPHONIC ACID-GUANYLATE ESTER Authors: Franken, S.M, Scheidig, A.J, Wittinghofer, A, Goody, R.S. Deposit date: 1993-03-29 Release date: 1994-04-30 Last modified: 2024-02-07 Method: X-RAY DIFFRACTION (2.3 Å) Cite: Three-dimensional structures and properties of a transforming and a nontransforming glycine-12 mutant of p21H-ras. Biochemistry, 32, 1993
1CSL	CRYSTAL STRUCTURE OF THE RRE HIGH AFFINITY SITE Descriptor: 5'-R(*AP*AP*CP*GP*GP*GP*CP*GP*CP*AP*GP*AP*A)-3', 5'-R(*UP*CP*UP*GP*AP*CP*GP*GP*UP*AP*CP*GP*UP*UP*U)-3' Authors: Ippolito, J.A, Steitz, T.A. Deposit date: 1999-08-18 Release date: 2000-02-14 Last modified: 2024-02-07 Method: X-RAY DIFFRACTION (1.6 Å) Cite: The structure of the HIV-1 RRE high affinity rev binding site at 1.6 A resolution. J.Mol.Biol., 295, 2000
1AL4	GRAMICIDIN D FROM BACILLUS BREVIS (N-PROPANOL SOLVATE) Descriptor: GRAMICIDIN D, N-PROPANOL Authors: Burkhart, B.M, Gassman, R.M, Pangborn, W.A, Duax, W.L. Deposit date: 1997-06-11 Release date: 1998-03-04 Last modified: 2023-11-15 Method: X-RAY DIFFRACTION (1.13 Å) Cite: Heterodimer Formation and Crystal Nucleation of Gramicidin D Biophys.J., 75, 1998
134D	SOLUTION STRUCTURE OF A PURINE(DOT)PURINE(DOT)PYRIMIDINE DNA TRIPLEX CONTAINING G(DOT)GC AND T(DOT)AT TRIPLES Descriptor: DNA TRIPLEX Authors: Patel, D.J, Radhakrishnan, I. Deposit date: 1993-08-30 Release date: 1994-04-30 Last modified: 2024-04-10 Method: SOLUTION NMR Cite: Solution structure of a purine.purine.pyrimidine DNA triplex containing G.GC and T.AT triples. Structure, 1, 1993
1AYW	CRYSTAL STRUCTURE OF CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT BENZYLOXYBENZOYLCARBOHYDRAZIDE INHIBITOR Descriptor: 1-(N-BENZYLOXYCARBONYL-L-LEUCINYL)-5-(3-BENZYLOXY BENZOYL)CARBOHYDRAZIDE, CATHEPSIN K Authors: Zhao, B, Smith, W.W, Janson, C.A, Abdel-Meguid, S.S. Deposit date: 1997-11-10 Release date: 1998-11-25 Last modified: 2023-08-02 Method: X-RAY DIFFRACTION (2.4 Å) Cite: Design of potent and selective human cathepsin K inhibitors that span the active site. Proc.Natl.Acad.Sci.USA, 94, 1997
1APS	THREE-DIMENSIONAL STRUCTURE OF ACYLPHOSPHATASE. REFINEMENT AND STRUCTURE ANALYSIS Descriptor: ACYLPHOSPHATASE Authors: Saudek, V, Pastore, A, Ramponi, G, Williams, R.J.P. Deposit date: 1991-02-20 Release date: 1992-07-15 Last modified: 2024-05-22 Method: SOLUTION NMR Cite: Three-dimensional structure of acylphosphatase. Refinement and structure analysis. J.Mol.Biol., 224, 1992
1BD8	STRUCTURE OF CDK INHIBITOR P19INK4D Descriptor: P19INK4D CDK4/6 INHIBITOR Authors: Baumgartner, R, Fernandez-Catalan, C, Winoto, A, Huber, R, Engh, R, Holak, T.A. Deposit date: 1998-05-12 Release date: 1998-10-14 Last modified: 2024-02-07 Method: X-RAY DIFFRACTION (1.8 Å) Cite: Structure of human cyclin-dependent kinase inhibitor p19INK4d: comparison to known ankyrin-repeat-containing structures and implications for the dysfunction of tumor suppressor p16INK4a. Structure, 6, 1998
1CQ2	NEUTRON STRUCTURE OF FULLY DEUTERATED SPERM WHALE MYOGLOBIN AT 2.0 ANGSTROM Descriptor: MYOGLOBIN, PROTOPORPHYRIN IX CONTAINING FE Authors: Shu, F, Ramakrishnan, V, Schoenborn, B.P. Deposit date: 1999-08-04 Release date: 1999-08-16 Last modified: 2024-02-07 Method: NEUTRON DIFFRACTION (2 Å) Cite: Enhanced visibility of hydrogen atoms by neutron crystallography on fully deuterated myoglobin. Proc.Natl.Acad.Sci.USA, 97, 2000
1D7E	CRYSTAL STRUCTURE OF THE P65 CRYSTAL FORM OF PHOTOACTIVE YELLOW PROTEIN Descriptor: 4'-HYDROXYCINNAMIC ACID, PHOTOACTIVE YELLOW PROTEIN Authors: Van Aalten, D.M.F, Crielaard, W, Hellingwerf, K.J, Joshua-Tor, L. Deposit date: 1999-10-17 Release date: 2000-03-31 Last modified: 2018-01-31 Method: X-RAY DIFFRACTION (1.39 Å) Cite: Conformational substates in different crystal forms of the photoactive yellow protein--correlation with theoretical and experimental flexibility. Protein Sci., 9, 2000

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