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1E7K
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Crystal structure of the spliceosomal 15.5kD protein bound to a U4 snRNA fragment
分子名称: 15.5 KD RNA BINDING PROTEIN, RNA (5'-R(*GP*CP*CP*AP*AP*UP*GP*AP*GP*GP*UP*UP*UP* AP*UP*CP*CP*GP*AP*GP*G*C(-3')
著者Vidovic, I, Nottrott, S, Harthmuth, K, Luhrmann, R, Ficner, R.
登録日2000-08-29
公開日2001-02-19
最終更新日2024-05-08
実験手法X-RAY DIFFRACTION (2.9 Å)
主引用文献Crystal Structure of the Spliceosomal 15.5Kd Protein Bound to a U4 Snrna Fragment
Mol.Cell, 6, 2000
1E7L
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Endonuclease VII (EndoVII) N62D mutant from phage T4
分子名称: RECOMBINATION ENDONUCLEASE VII, SULFATE ION, ZINC ION
著者Raaijmakers, H.C.A, Vix, O, Toro, I, Suck, D.
登録日2000-08-29
公開日2001-05-04
最終更新日2024-05-08
実験手法X-RAY DIFFRACTION (1.32 Å)
主引用文献Conformational Flexibility in T4 Endonuclease Vii Revealed by Crystallography: Implications for Substrate Binding and Cleavage
J.Mol.Biol., 308, 2001
1E7M
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ACTIVE SITE MUTANT (D177->N) OF GLUCOSE 6-PHOSPHATE DEHYDROGENASE FROM LEUCONOSTOC MESENTEROIDES
分子名称: CALCIUM ION, GLUCOSE 6-PHOSPHATE 1-DEHYDROGENASE
著者Adams, M.J, Cosgrove, M.S, Gover, S.
登録日2000-08-30
公開日2000-12-11
最終更新日2024-05-01
実験手法X-RAY DIFFRACTION (2.54 Å)
主引用文献An Examination of the Role of Asp-177 in the His-Asp Catalytic Dyad of Leuconostoc Mesenteroides Glucose 6-Phosphate Dehydrogenase: X-Ray Structure and Ph Dependence of Kinetic Parameters of the D177N Mutant Enzyme
Biochemistry, 39, 2000
1E7N
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The N-terminal domain of beta-B2-crystallin resembles the putative ancestral homodimer
分子名称: BETA-CRYSTALLIN B2
著者Clout, N.J, Basak, A, Wieligmann, K, Bateman, O.A, Jaenicke, R, Slingsby, C.
登録日2000-08-31
公開日2000-10-05
最終更新日2024-05-08
実験手法X-RAY DIFFRACTION (2.35 Å)
主引用文献The N-Terminal Domain of Betab2-Crystallin Resembles the Putative Ancestral Homodimer.
J.Mol.Biol., 304, 2000
1E7O
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A-SPECTRIN SH3 DOMAIN A11V, V23L, M25V, V44I, V58L MUTATIONS
分子名称: GLYCEROL, SPECTRIN ALPHA CHAIN
著者Vega, M.C, Serrano, L.
登録日2000-08-31
公開日2003-05-21
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (3.2 Å)
主引用文献A Thermodynamic and Kinetic Analysis of the Folding Pathway of an SH3 Domain Entropically Stabilised by a Redesigned Hydrophobic Core
J.Mol.Biol., 328, 2003
1E7P
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QUINOL:FUMARATE REDUCTASE FROM WOLINELLA SUCCINOGENES
分子名称: DODECYL-BETA-D-MALTOSIDE, FE2/S2 (INORGANIC) CLUSTER, FE3-S4 CLUSTER, ...
著者Lancaster, C.R.D, Kroeger, A.
登録日2000-09-01
公開日2001-04-09
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (3.1 Å)
主引用文献A Third Crystal Form of Wolinella Succinogenes Quinol:Fumarate Reductase Reveals Domain Closure at the Site of Fumarate Reduction
Eur.J.Biochem., 268, 2001
1E7Q
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GDP 4-keto-6-deoxy-D-mannose epimerase reductase S107A
分子名称: 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, ACETYLPHOSPHATE, GDP-FUCOSE SYNTHETASE, ...
著者Rosano, C, Izzo, G, Bolognesi, M.
登録日2000-09-07
公開日2000-10-18
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (1.6 Å)
主引用文献Probing the Catalytic Mechanism of Gdp-4-Keto-6-Deoxy-D-Mannose Epimerase/Reductase by Kinetic and Crystallographic Characterization of Site-Specific Mutants
J.Mol.Biol., 303, 2000
1E7R
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GDP 4-keto-6-deoxy-D-mannose epimerase reductase Y136E
分子名称: 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, ACETYLPHOSPHATE, GDP-FUCOSE SYNTHETASE, ...
著者Rosano, C, Izzo, G, Bolognesi, M.
登録日2000-09-07
公開日2000-10-18
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (1.6 Å)
主引用文献Probing the Catalytic Mechanism of Gdp-4-Keto-6-Deoxy-D-Mannose Epimerase/Reductase by Kinetic and Crystallographic Characterization of Site-Specific Mutants
J.Mol.Biol., 303, 2000
1E7S
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GDP 4-keto-6-deoxy-D-mannose epimerase reductase K140R
分子名称: 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, ACETYLPHOSPHATE, GDP-FUCOSE SYNTHETASE, ...
著者Rosano, C, Zuccotti, S, Izzo, G, Bolognesi, M.
登録日2000-09-07
公開日2000-10-18
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (1.5 Å)
主引用文献Probing the Catalytic Mechanism of Gdp-4-Keto-6-Deoxy-D-Mannose Epimerase/Reductase by Kinetic and Crystallographic Characterization of Site-Specific Mutants
J.Mol.Biol., 303, 2000
1E7U
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Structure determinants of phosphoinositide 3-kinase inhibition by wortmannin, LY294002, quercetin, myricetin and staurosporine
分子名称: (1S,6BR,9AS,11R,11BR)-9A,11B-DIMETHYL-1-[(METHYLOXY)METHYL]-3,6,9-TRIOXO-1,6,6B,7,8,9,9A,10,11,11B-DECAHYDRO-3H-FURO[4, 3,2-DE]INDENO[4,5-H][2]BENZOPYRAN-11-YL ACETATE, PHOSPHATIDYLINOSITOL 3-KINASE CATALYTIC SUBUNIT
著者Walker, E.H, Perisic, O, Ried, C, Stephens, L, Williams, R.L.
登録日2000-09-08
公開日2000-11-17
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Structural Determinations of Phosphoinositide 3-Kinase Inhibition by Wortmannin, Ly294002, Quercetin, Myricetin and Staurosporine
Mol.Cell, 6, 2000
1E7V
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Structure determinants of phosphoinositide 3-kinase inhibition by wortmannin, LY294002, quercetin, myricetin and staurosporine
分子名称: 2-MORPHOLIN-4-YL-7-PHENYL-4H-CHROMEN-4-ONE, PHOSPHATIDYLINOSITOL 3-KINASE CATALYTIC SUBUNIT
著者Walker, E.H, Pacold, M.E, Perisic, O, Stephens, L, Hawkins, P.T, Wymann, M.P, Williams, R.L.
登録日2000-09-08
公開日2000-11-17
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (2.4 Å)
主引用文献Structural determinants of phosphoinositide 3-kinase inhibition by wortmannin, LY294002, quercetin, myricetin, and staurosporine.
Mol.Cell, 6, 2000
1E7W
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One active site, two modes of reduction correlate the mechanism of leishmania pteridine reductase with pterin metabolism and antifolate drug resistance in trpanosomes
分子名称: 1,2-ETHANEDIOL, METHOTREXATE, NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, ...
著者Gourley, D.G, Hunter, W.N.
登録日2000-09-11
公開日2001-09-06
最終更新日2024-05-08
実験手法X-RAY DIFFRACTION (1.75 Å)
主引用文献Pteridine Reductase Mechanism Correlates Pterin Metabolism with Drug Resistance in Trypanosomatid Parasites.
Nat.Struct.Biol., 8, 2001
1E7Y
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ACTIVE SITE MUTANT (D177->N) OF GLUCOSE 6-PHOSPHATE DEHYDROGENASE FROM LEUCONOSTOC MESENTEROIDES COMPLEXED WITH SUBSTRATE AND NADPH
分子名称: 6-O-phosphono-beta-D-glucopyranose, CALCIUM ION, GLUCOSE 6-PHOSPHATE 1-DEHYDROGENASE, ...
著者Adams, M.J, Cosgrove, M.S, Gover, S.
登録日2000-09-12
公開日2000-12-11
最終更新日2024-05-01
実験手法X-RAY DIFFRACTION (2.48 Å)
主引用文献An Examination of the Role of Asp-177 in the His-Asp Catalytic Dyad of Leuconostoc Mesenteroides Glucose 6-Phosphate Dehydrogenase: X-Ray Structure and Ph Dependence of Kinetic Parameters of the D177N Mutant Enzyme
Biochemistry, 39, 2000
1E7Z
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Crystal structure of the EMAP2/RNA binding domain of the p43 protein from human aminoacyl-tRNA synthetase complex
分子名称: ENDOTHELIAL-MONOCYTE ACTIVATING POLYPEPTIDE II, MERCURY (II) ION
著者Pasqualato, S, Kerjan, P, Renault, L, Menetrey, J, Mirande, M, Cherfils, J.
登録日2000-09-13
公開日2000-11-27
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (2.05 Å)
主引用文献Structure of the Emapii Domain of Human Aminoacyl-tRNA Synthetase Complex Reveals Evolutionary Dimeric Mimicry
Embo J., 20, 2001
1E80
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Endothiapepsin complex with renin inhibitor MERCK-KGAA-EMD56133
分子名称: 4-amino-N-{(1R,8R,9R,13R)-16-(4-amino-2-methylpyrimidin-5-yl)-1-benzyl-8-(cyclohexylmethyl)-9-hydroxy-13-[(1S)-1-methylpropyl]-2,6,11,14-tetraoxo-3,7,12,15-tetraazahexadec-1-yl}piperidine-1-carboxamide, ENDOTHIAPEPSIN
著者Read, J.A, Cooper, J.B, Toldo, L, Rippmann, F, Raddatz, P.
登録日2000-09-15
公開日2000-09-26
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (2.05 Å)
主引用文献Refinement of Four Endothiapepsin Inhibitor Complexes. Crystallographic Studies of Cytochrome Ch from Methylobacterium Extorquens and Inhibitor Complexes of Aspartic Proteinases.
Ph D Thesis, 1999
1E81
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Endothiapepsin complex with renin inhibitor MERCK-KGAA-EMD61395
分子名称: (2S)-1-{[(2R)-1-{[(2S,3S)-1-cyclohexyl-3-hydroxy-4-(2-oxopyridin-1(2H)-yl)butan-2-yl]amino}-3-(methylsulfanyl)-1-oxopropan-2-yl]amino}-1-oxo-3-phenylpropan-2-yl 4-aminopiperidine-1-carboxylate, ENDOTHIAPEPSIN
著者Read, J.A, Cooper, J.B, Toldo, L, Rippmann, F, Raddatz, P.
登録日2000-09-15
公開日2000-10-19
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (2.05 Å)
主引用文献Refinement of Four Endothiapepsin Inhibitor Complexes. Crystallographic Studies of Cytochrome Ch from Methylobacterium Extorquens and Inhibitor Complexes of Aspartic Proteinases.
Thesis, 1999
1E82
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Endothiapepsin complex with renin inhibitor MERCK-KGAA-EMD59601
分子名称: (2S)-1-{[(2R)-1-{[(2S,3R)-1-cyclohexyl-3-hydroxy-4-(pyridin-4-yloxy)butan-2-yl]amino}-3-(methylsulfanyl)-1-oxopropan-2-yl]amino}-1-oxo-3-phenylpropan-2-yl 4-aminopiperidine-1-carboxylate, ENDOTHIAPEPSIN
著者Read, J.A, Cooper, J.B, Toldo, L, Rippmann, F, Raddatz, P.
登録日2000-09-15
公開日2000-10-19
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (2.05 Å)
主引用文献Refinement of Four Endothiapepsin Inhibitor Complexes. Crystallographic Studies of Cytochrome Ch from Methylobacterium Extorquens and Inhibitor Complexes of Aspartic Proteinases.
Thesis, 1999
1E83
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Cytochrome c' from Alcaligenes xylosoxidans - oxidized structure
分子名称: CYTOCHROME C', HEME C
著者Lawson, D.M, Stevenson, C.E.M, Andrew, C.R, Eady, R.R.
登録日2000-09-15
公開日2000-11-06
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (2.05 Å)
主引用文献Unprecedented Proximal Binding of Nitric Oxide to Heme: Implications for Guanylate Cyclase
Embo J., 19, 2000
1E84
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Cytochrome c' from Alcaligenes xylosoxidans - reduced structure
分子名称: CYTOCHROME C', HEME C
著者Lawson, D.M, Stevenson, C.E.M, Andrew, C.R, Eady, R.R.
登録日2000-09-15
公開日2000-11-06
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献Unprecedented Proximal Binding of Nitric Oxide to Heme: Implications for Guanylate Cyclase
Embo J., 19, 2000
1E85
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Cytochrome c' from Alcaligenes xylosoxidans - reduced structure with NO bound to proximal side of heme
分子名称: CYTOCHROME C', HEME C, NITRIC OXIDE
著者Lawson, D.M, Stevenson, C.E.M, Andrew, C.R, Eady, R.R.
登録日2000-09-15
公開日2000-11-06
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (1.35 Å)
主引用文献Unprecedented Proximal Binding of Nitric Oxide to Heme: Implications for Guanylate Cyclase.
Embo J., 19, 2000
1E86
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Cytochrome c' from Alcaligenes xylosoxidans - reduced structure with CO bound to distal side of heme
分子名称: CARBON MONOXIDE, CYTOCHROME C', HEME C
著者Lawson, D.M, Stevenson, C.E.M, Andrew, C.R, Eady, R.R.
登録日2000-09-15
公開日2000-11-06
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (1.95 Å)
主引用文献Unprecedented Proximal Binding of Nitric Oxide to Heme: Implications for Guanylate Cyclase
Embo J., 19, 2000
1E87
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Human CD69 - trigonal form
分子名称: EARLY ACTIVATION ANTIGEN CD69, GLYCEROL, ZINC ION
著者Tormo, J.
登録日2000-09-18
公開日2000-09-26
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (1.5 Å)
主引用文献Crystal Structure of the C-Type Lectin-Like Domain from the Human Hematopoietic Cell Receptor Cd69
J.Biol.Chem., 276, 2001
1E88
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Solution structure of 6F11F22F2, a compact three-module fragment of the gelatin-binding domain of human fibronectin
分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose, FIBRONECTIN
著者Pickford, A.R, Smith, S.P, Staunton, D, Boyd, J, Campbell, I.D.
登録日2000-09-18
公開日2000-10-09
最終更新日2020-07-29
実験手法SOLUTION NMR
主引用文献The Hairpin Structure of the (6)F1(1)F2(2)F2 Fragment from Human Fibronectin Enhances Gelatin Binding
Embo J., 20, 2001
1E89
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ON THE MECHANISM OF CYANOGENESIS CATALYZED BY HYDROXYNITRILE LYASE FROM MANIHOT ESCULENTA. CRYSTAL STRUCTURE OF ACTIVE SITE MUTANT SER80ALA IN COMPLEX WITH ACETONE CYANOHYDRIN
分子名称: HYDROXYNITRILE LYASE
著者Lauble, H, Miehlich, B, Foerster, S, Wajant, H, Effenberger, F.
登録日2000-09-18
公開日2001-08-17
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (2.1 Å)
主引用文献Mechanistic Aspects of Cyanogenesis from Active-Site Mutant Ser80Ala of Hydroxynitrile Lyase from Manihot Esculenta in Complex with Acetone Cyanohydrin
Protein Sci., 10, 2001
1E8A
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The three-dimensional structure of human S100A12
分子名称: CALCIUM ION, S100A12
著者Moroz, O.V, Antson, A.A, Murshudov, G.N, Maitland, N.J, Dodson, G.G, Wilson, K.S, Skibshoj, I, Lukanidin, E.M, Bronstein, I.B.
登録日2000-09-18
公開日2001-01-08
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (1.95 Å)
主引用文献The Three-Dimensional Structure of Human S100A12
Acta Crystallogr.,Sect.D, 57, 2001

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