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PDB: 5628 件
8DBI
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Human PRPS1 with Phosphate, ATP, and R5P; Hexamer
分子名称: 5-O-phosphono-alpha-D-ribofuranose, ADENOSINE-5'-TRIPHOSPHATE, MAGNESIUM ION, ...
著者Hvorecny, K.L, Kollman, J.M.
登録日2022-06-14
公開日2023-02-15
最終更新日2024-06-12
実験手法ELECTRON MICROSCOPY (2 Å)
主引用文献Human PRPS1 filaments stabilize allosteric sites to regulate activity.
Nat.Struct.Mol.Biol., 30, 2023
8DBH
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Human PRPS1 with Phosphate and ATP; Filament Interface
分子名称: ADENOSINE-5'-TRIPHOSPHATE, MAGNESIUM ION, PHOSPHATE ION, ...
著者Hvorecny, K.L, Kollman, J.M.
登録日2022-06-14
公開日2023-02-15
最終更新日2024-06-12
実験手法ELECTRON MICROSCOPY (2.2 Å)
主引用文献Human PRPS1 filaments stabilize allosteric sites to regulate activity.
Nat.Struct.Mol.Biol., 30, 2023
1XMI
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Crystal structure of human F508A NBD1 domain with ATP
分子名称: ADENOSINE-5'-TRIPHOSPHATE, Cystic fibrosis transmembrane conductance regulator, MAGNESIUM ION
著者Lewis, H.A, Zhao, X, Wang, C, Sauder, J.M, Rooney, I, Noland, B.W, Lorimer, D, Kearins, M.C, Conners, K, Condon, B, Maloney, P.C, Guggino, W.B, Hunt, J.F, Emtage, S, Structural GenomiX
登録日2004-10-02
公開日2004-11-09
最終更新日2023-08-23
実験手法X-RAY DIFFRACTION (2.25 Å)
主引用文献Impact of the delta-F508 Mutation in First Nucleotide-binding Domain of Human Cystic Fibrosis Transmembrane Conductance Regulator on Domain Folding and Structure
J.Biol.Chem., 280, 2005
2XWD
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X-RAY STRUCTURE OF ACID-BETA-GLUCOSIDASE WITH 5N,6O-(N'-(N-OCTYL)IMINO)NOJIRIMYCIN IN THE ACTIVE SITE
分子名称: (3Z,5S,6R,7S,8R,8aR)-3-(octylimino)hexahydro[1,3]oxazolo[3,4-a]pyridine-5,6,7,8-tetrol, GLUCOSYLCERAMIDASE, SULFATE ION, ...
著者Brumshtein, B, Aguilar-Moncayo, M, Benito, J.M, Ortiz Mellet, C, Garcia Fernandez, J.M, Silman, I, Shaaltiel, Y, Sussman, J.L, Futerman, A.H.
登録日2010-11-01
公開日2011-09-14
最終更新日2023-12-20
実験手法X-RAY DIFFRACTION (2.66 Å)
主引用文献Cyclodextrin-Mediated Crystallization of Acid Beta-Glucosidase in Complex with Amphiphilic Bicyclic Nojirimycin Analogues.
Org.Biomol.Chem., 9, 2011
1X8E
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Crystal structure of Pyrococcus furiosus phosphoglucose isomerase free enzyme
分子名称: Glucose-6-phosphate isomerase
著者Berrisford, J.M, Akerboom, J, Brouns, S, Sedelnikova, S.E, Turnbull, A.P, van der Oost, J, Salmon, L, Hardre, R, Murray, I.A, Blackburn, G.M, Rice, D.W, Baker, P.J.
登録日2004-08-18
公開日2004-10-12
最終更新日2023-08-23
実験手法X-RAY DIFFRACTION (2.8 Å)
主引用文献The structures of inhibitor complexes of Pyrococcus furiosus phosphoglucose isomerase provide insights into substrate binding and catalysis.
J.Mol.Biol., 343, 2004
1XOD
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Crystal structure of X. tropicalis Spred1 EVH-1 domain
分子名称: GLYCEROL, Spred1
著者Harmer, N.J, Sivak, J.M, Amaya, E, Blundell, T.L.
登録日2004-10-06
公開日2005-01-25
最終更新日2023-08-23
実験手法X-RAY DIFFRACTION (1.15 Å)
主引用文献1.15A Crystal structure of the X. tropicalis Spred1 EVH1 domain suggests a fourth distinct peptide-binding mechanism within the EVH1 family
Febs Lett., 579, 2005
1XOK
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crystal structure of alfalfa mosaic virus RNA 3'UTR in complex with coat protein N terminal peptide
分子名称: BROMIDE ION, Coat protein, alfalfa mosaic virus RNA 3' UTR
著者Guogas, L.M, Filman, D.J, Hogle, J.M, Gehrke, L.
登録日2004-10-06
公開日2005-01-04
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (3 Å)
主引用文献Cofolding organizes alfalfa mosaic virus RNA and coat protein for replication.
Science, 306, 2004
1XGD
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Apo R268A human aldose reductase
分子名称: Aldose reductase
著者Brownlee, J.M, Bohren, K.M, Milne, A.C, Gabbay, K.H, Harrison, D.H.T.
登録日2004-09-16
公開日2005-03-29
最終更新日2023-08-23
実験手法X-RAY DIFFRACTION (2.1 Å)
主引用文献The structure of Apo R268A human aldose reductase: Hinges and latches that control the kinetic mechanism
Biochim.Biophys.Acta, 1748, 2005
8CTQ
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Crystal structure of engineered phospholipase D mutant superPLD 2-48
分子名称: PHOSPHATE ION, Phospholipase D
著者Tei, R, Bagde, S.R, Fromme, J.C, Baskin, J.M.
登録日2022-05-16
公開日2023-04-26
最終更新日2023-10-25
実験手法X-RAY DIFFRACTION (1.85 Å)
主引用文献Activity-based directed evolution of a membrane editor in mammalian cells.
Nat.Chem., 15, 2023
1XPR
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Structural mechanism of inhibition of the Rho transcription termination factor by the antibiotic 5a-formylbicyclomycin (FB)
分子名称: 5'-R(*CP*UP*CP*UP*CP*UP*CP*U)-3', 5A-FORMYLBICYCLOMYCIN, MAGNESIUM ION, ...
著者Skordalakes, E, Brogan, A.P, Park, B.S, Kohn, H, Berger, J.M.
登録日2004-10-09
公開日2004-11-02
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (3.15 Å)
主引用文献Structural mechanism of inhibition of the rho transcription termination factor by the antibiotic bicyclomycin
Structure, 13, 2005
1XQ9
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Structure of Phosphoglycerate Mutase from Plasmodium falciparum at 2.6 Resolution
分子名称: THIOCYANATE ION, phosphoglycerate mutase
著者Caruthers, J.M, Hol, W.G.J, Structural Genomics of Pathogenic Protozoa Consortium (SGPP)
登録日2004-10-11
公開日2004-12-21
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (2.58 Å)
主引用文献Structure of Phosphoglycerate Mutase from Plasmodium falciparum at 2.6 Resolution
TO BE PUBLISHED
5OTG
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Crystal Structure of the Protein-Kinase A catalytic subunit from Criteculus Griseus in complex with compounds RKp013 and RKp190
分子名称: [2-[[2-(isoquinolin-5-ylsulfonylamino)ethylamino]methyl]phenyl]boronic acid, cAMP-dependent protein kinase catalytic subunit alpha, cAMP-dependent protein kinase inhibitor
著者Mueller, J.M, Heine, A, Klebe, G.
登録日2017-08-21
公開日2018-09-05
実験手法X-RAY DIFFRACTION (1.73 Å)
主引用文献Crystal Structure of the Protein-Kinase A catalytic subunit from Criteculus Griseus in complex with compounds RKp013 and RKp190
To be published
8ERN
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Cyclin-free CDK2 in complex with Cpd21
分子名称: Cyclin-dependent kinase 2, GLYCEROL, N,3-dimethyl-4-({7-[(2S)-2-methylpyrrolidine-1-carbonyl]quinazolin-2-yl}amino)benzene-1-sulfonamide
著者Murray, J.M, Oh, A.
登録日2022-10-12
公開日2023-10-18
実験手法X-RAY DIFFRACTION (1.64 Å)
主引用文献Cyclin-free CDK2 in complex with Cpd21
To Be Published
1UVI
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The structural basis for RNA specificity and Ca2 inhibition of an RNA-dependent RNA polymerase phi6p2 with 6nt RNA
分子名称: 5'-R(*UP*UP*UP*UP*CP*CP)-3', MANGANESE (II) ION, RNA-directed RNA polymerase
著者Salgado, P.S, Makeyev, E.V, Butcher, S, Bamford, D, Stuart, D.I, Grimes, J.M.
登録日2004-01-21
公開日2004-02-19
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (2.15 Å)
主引用文献The structural basis for RNA specificity and Ca2+ inhibition of an RNA-dependent RNA polymerase.
Structure, 12, 2004
8ERD
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Cyclin-free CDK2 in complex with Cpd17
分子名称: (2-{[1-(methanesulfonyl)piperidin-4-yl]amino}quinazolin-7-yl)[(2S)-2-methylpyrrolidin-1-yl]methanone, Cyclin-dependent kinase 2
著者Murray, J.M, Oh, A.
登録日2022-10-11
公開日2023-10-18
実験手法X-RAY DIFFRACTION (1.33 Å)
主引用文献Cyclin-free CDK2 in complex with Cpd17
To Be Published
1UUZ
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IVY:A NEW FAMILY OF PROTEIN
分子名称: INHIBITOR OF VERTEBRATE LYSOZYME, LYSOZYME C
著者Abergel, C, Lembo, F, Byrne, D, Maza, C, Claverie, J.M.
登録日2004-01-12
公開日2004-01-14
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (1.8 Å)
主引用文献Structure and Evolution of the Ivy Protein Family, Unexpected Lysozyme Inhibitors in Gram-Negative Bacteria.
Proc.Natl.Acad.Sci.USA, 104, 2007
2PLV
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STRUCTURAL FACTORS THAT CONTROL CONFORMATIONAL TRANSITIONS AND SEROTYPE SPECIFICITY IN TYPE 3 POLIOVIRUS
分子名称: HUMAN POLIOVIRUS TYPE 1 (SUBUNIT VP1), HUMAN POLIOVIRUS TYPE 1 (SUBUNIT VP2), HUMAN POLIOVIRUS TYPE 1 (SUBUNIT VP3), ...
著者Filman, D.J, Hogle, J.M.
登録日1989-10-17
公開日1989-10-17
最終更新日2023-04-19
実験手法X-RAY DIFFRACTION (2.88 Å)
主引用文献Structural factors that control conformational transitions and serotype specificity in type 3 poliovirus
EMBO J., 8, 1989
1XQ7
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Cyclophilin from Trypanosoma cruzi bound to cyclosporin A
分子名称: CYCLOSPORIN A, PEPTIDYL-PROLYL CIS-TRANS ISOMERASE
著者Caruthers, J.M, Hol, W.G.J, Structural Genomics of Pathogenic Protozoa Consortium (SGPP)
登録日2004-10-11
公開日2004-12-21
最終更新日2023-11-15
実験手法X-RAY DIFFRACTION (2.07 Å)
主引用文献Cyclophilin from Trypanosoma Cruzi Bound to Cyclosporin A
To be Published
1XUJ
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TRYPSIN-KETO-BABIM-ZN+2, PH 8.2
分子名称: BIS(5-AMIDINO-BENZIMIDAZOLYL)METHANONE ZINC, CALCIUM ION, SULFATE ION, ...
著者Katz, B.A, Clark, J.M, Finer-Moore, J.S, Jenkins, T.E, Johnson, C.R, Rose, M.J, Luong, C, Moore, W.R, Stroud, R.M.
登録日1997-10-10
公開日1998-11-11
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (1.92 Å)
主引用文献Design of potent selective zinc-mediated serine protease inhibitors.
Nature, 391, 1998
1XIP
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Crystal Structure of the N-terminal Domain of Nup159
分子名称: Nucleoporin NUP159
著者Weirich, C.S, Erzberger, J.P, Berger, J.M, Weis, K.
登録日2004-09-21
公開日2004-12-14
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (2.5 Å)
主引用文献The N-Terminal Domain of Nup159 Forms a beta-Propeller that Functions in mRNA Export by Tethering the Helicase Dbp5 to the Nuclear Pore
Mol.Cell, 16, 2004
1XUH
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TRYPSIN-KETO-BABIM-CO+2, PH 8.2
分子名称: BIS(5-AMIDINO-2-BENZIMIDAZOLYL)METHANONE, CALCIUM ION, COBALT (II) ION, ...
著者Katz, B.A, Clark, J.M, Finer-Moore, J.S, Jenkins, T.E, Johnson, C.R, Rose, M.J, Luong, C, Moore, W.R, Stroud, R.M.
登録日1997-10-10
公開日1998-11-11
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献Design of potent selective zinc-mediated serine protease inhibitors.
Nature, 391, 1998
1YH5
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Solution NMR Structure of Protein yggU from Escherichia coli. Northeast Structural Genomics Consortium Target ER14.
分子名称: ORF, HYPOTHETICAL PROTEIN
著者Aramini, J.M, Xiao, R, Huang, Y.J, Acton, T.B, Wu, M.J, Mills, J.L, Tejero, R.T, Szyperski, T, Montelione, G.T, Northeast Structural Genomics Consortium (NESG)
登録日2005-01-06
公開日2005-02-01
最終更新日2024-05-01
実験手法SOLUTION NMR
主引用文献Solution Structure of the Hypothetical Protein Yggu from E. Coli. Northeast Structural Genomics Consortium Target Er14.
To be Published
1Y50
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X-ray crystal structure of Bacillus stearothermophilus Histidine phosphocarrier protein (Hpr) F29W mutant domain_swapped dimer
分子名称: Phosphocarrier protein HPr, SULFATE ION
著者Sridharan, S, Razvi, A, Scholtz, J.M, Sacchettini, J.C.
登録日2004-12-01
公開日2005-02-22
最終更新日2024-04-03
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献The HPr proteins from the thermophile Bacillus stearothermophilus can form domain-swapped dimers.
J.Mol.Biol., 346, 2005
1Y5R
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The crystal structure of murine 11b-hydroxysteroid dehydrogenase complexed with corticosterone
分子名称: CORTICOSTERONE, Corticosteroid 11-beta-dehydrogenase, isozyme 1, ...
著者Zhang, J, Osslund, T.D, Plant, M.H, Clogston, C.L, Nybo, R.E, Xiong, F, Delaney, J.M, Jordan, S.
登録日2004-12-02
公開日2005-05-17
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (3 Å)
主引用文献Crystal Structure of Murine 11-Hydroxysteroid Dehydrogenase 1: An Important Therapeutic Target for Diabetes
Biochemistry, 44, 2005
8P9T
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Crystal structure of the metallo-beta-lactamase VIM1 with 2483
分子名称: 7-[(1~{S})-1-(4-azanylbutanoyloxy)ethyl]-3-[3-chloranyl-4-(methylsulfonylmethyl)phenyl]-1~{H}-indole-2-carboxylic acid, Beta-lactamase VIM-1, ZINC ION
著者Calvopina, K, Brem, J, Farley, A.J.M, Allen, M.D, Schofield, C.J.
登録日2023-06-06
公開日2024-06-26
実験手法X-RAY DIFFRACTION (1.2 Å)
主引用文献Crystal structure of the metallo-beta-lactamase VIM1 with 2483
To Be Published

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