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