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1I46
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The solution structure of the mutant stem loop C 5'GUA3' triloop of brome mosaic virus (+) strand RNA
分子名称: 5'-R(*GP*GP*UP*GP*CP*GP*UP*AP*GP*CP*AP*CP*C)-3'
著者Kim, C.-H, Tinoco Jr, I.
登録日2001-02-20
公開日2001-04-21
最終更新日2024-05-01
実験手法SOLUTION NMR
主引用文献Structural and thermodynamic studies on mutant RNA motifs that impair the specificity between a viral replicase and its promoter
J.Mol.Biol., 307, 2001
1I4C
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THE SOLUTION STRUCTURE OF THE MINOR FAMILY OF THE MUTANT STEM LOOP C 5'UUA3' TRILOOP OF BROME MOSAIC VIRUS (+) STRAND RNA
分子名称: RNA (5'-R(*GP*GP*UP*GP*CP*UP*UP*AP*GP*CP*AP*CP*C)-3')
著者Tinoco Jr, I, Kim, C.-H.
登録日2001-02-20
公開日2001-04-21
最終更新日2024-05-22
実験手法SOLUTION NMR
主引用文献Structural and thermodynamic studies on mutant RNA motifs that impair the specificity between a viral replicase and its promoter.
J.Mol.Biol., 307, 2001
1I4B
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The solution structure of the major family of the mutant stem loop C 5'UUA3' triloop of brome mosaic virus (+) strand RNA
分子名称: 5'-R(*GP*GP*UP*GP*CP*UP*UP*AP*GP*CP*AP*CP*C)-3'
著者Tinoco Jr, I, Kim, C.-H.
登録日2001-02-20
公開日2001-04-21
最終更新日2024-05-22
実験手法SOLUTION NMR
主引用文献Structural and thermodynamic studies on mutant RNA motifs that impair the specificity between a viral replicase and its promoter
J.Mol.Biol., 307, 2001
6VLC
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Crystal structure of UDP-GlcNAc 2-epimerase from Neisseria meningitidis bound to UDP-GlcNAc
分子名称: UDP-N-acetylglucosamine 2-epimerase, URIDINE-DIPHOSPHATE-N-ACETYLGLUCOSAMINE
著者Fisher, A.J, Hurlburt, N.K.
登録日2020-01-23
公開日2020-11-11
最終更新日2023-10-11
実験手法X-RAY DIFFRACTION (2.15 Å)
主引用文献Structural characterization of a nonhydrolyzing UDP-GlcNAc 2-epimerase from Neisseria meningitidis serogroup A.
Acta Crystallogr.,Sect.F, 76, 2020
3IT0
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Crystal Structure Francisella tularensis histidine acid phosphatase complexed with phosphate
分子名称: 2-(2-METHOXYETHOXY)ETHANOL, Acid phosphatase, PENTAETHYLENE GLYCOL, ...
著者Singh, H, Felts, R.L, Reilly, T.J, Tanner, J.J.
登録日2009-08-27
公開日2009-11-10
最終更新日2023-09-06
実験手法X-RAY DIFFRACTION (1.692 Å)
主引用文献Crystal Structures of the histidine acid phosphatase from Francisella tularensis provide insight into substrate recognition.
J.Mol.Biol., 394, 2009
3IT2
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Crystal structure of ligand-free Francisella tularensis histidine acid phosphatase
分子名称: ACETATE ION, Acid phosphatase
著者Singh, H, Felts, R.L, Reilly, T.J, Tanner, J.J.
登録日2009-08-27
公開日2009-11-10
最終更新日2023-09-06
実験手法X-RAY DIFFRACTION (1.838 Å)
主引用文献Crystal Structures of the histidine acid phosphatase from Francisella tularensis provide insight into substrate recognition.
J.Mol.Biol., 394, 2009
3IT3
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Crystal Structure Francisella tularensis histidine acid phosphatase D261A mutant complexed with substrate 3'-AMP
分子名称: Acid phosphatase, [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] dihydrogen phosphate
著者Singh, H, Felts, R.L, Reilly, T.J, Tanner, J.J.
登録日2009-08-27
公開日2009-11-10
最終更新日2023-09-06
実験手法X-RAY DIFFRACTION (1.5 Å)
主引用文献Crystal Structures of the histidine acid phosphatase from Francisella tularensis provide insight into substrate recognition.
J.Mol.Biol., 394, 2009
3IT1
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Crystal Structure Francisella tularensis histidine acid phosphatase complexed with L(+)-tartrate
分子名称: 2-(2-METHOXYETHOXY)ETHANOL, ACETATE ION, Acid phosphatase, ...
著者Singh, H, Felts, R.L, Reilly, T.J, Tanner, J.J.
登録日2009-08-27
公開日2009-11-10
最終更新日2024-02-21
実験手法X-RAY DIFFRACTION (1.691 Å)
主引用文献Crystal Structures of the histidine acid phosphatase from Francisella tularensis provide insight into substrate recognition.
J.Mol.Biol., 394, 2009
4WVE
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Crystal structure of the Staphylococcus aureus SasG G52-E2-G53 module
分子名称: CHLORIDE ION, Surface protein G
著者Whelan, F, Potts, J.R.
登録日2014-11-05
公開日2015-06-03
最終更新日2024-01-10
実験手法X-RAY DIFFRACTION (1.6 Å)
主引用文献Cooperative folding of intrinsically disordered domains drives assembly of a strong elongated protein.
Nat Commun, 6, 2015
5J5Q
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AMP-PNP-stabilized ATPase domain of topoisomerase IV from Streptococcus pneumoniae, complex type II
分子名称: DNA (5'-D(*GP*CP*AP*TP*AP*TP*AP*TP*AP*TP*AP*TP*GP*C)-3'), DNA topoisomerase 4 subunit B, MAGNESIUM ION, ...
著者Laponogov, I, Pan, X.-S, Skamrova, G, Umrekar, T, Fisher, L.M, Sanderson, M.R.
登録日2016-04-03
公開日2017-07-26
最終更新日2024-01-10
実験手法X-RAY DIFFRACTION (2.83 Å)
主引用文献Trapping of the transport-segment DNA by the ATPase domains of a type II topoisomerase.
Nat Commun, 9, 2018
3C3B
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Crystal Structure of human phosphoglycerate kinase bound to D-CDP
分子名称: CYTIDINE-5'-DIPHOSPHATE, PHOSPHATE ION, Phosphoglycerate kinase 1
著者Arold, S.T, Gondeau, C, Lionne, C, Chaloin, L.
登録日2008-01-28
公開日2008-07-01
最終更新日2023-11-01
実験手法X-RAY DIFFRACTION (1.8 Å)
主引用文献Molecular basis for the lack of enantioselectivity of human 3-phosphoglycerate kinase
Nucleic Acids Res., 36, 2008
3C3A
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Crystal Structure of human phosphoglycerate kinase bound to 3-phosphoglycerate and L-ADP
分子名称: 3-PHOSPHOGLYCERIC ACID, ADENOSINE-5'-DIPHOSPHATE, MAGNESIUM ION, ...
著者Arold, S.T, Gondeau, C, Lionne, C, Chaloin, L.
登録日2008-01-28
公開日2008-07-01
最終更新日2023-11-01
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Molecular basis for the lack of enantioselectivity of human 3-phosphoglycerate kinase
Nucleic Acids Res., 36, 2008
3BQD
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Doubling the Size of the Glucocorticoid Receptor Ligand Binding Pocket by Deacylcortivazol
分子名称: 1-[(1R,2R,3aS,3bS,10aR,10bS,11S,12aS)-1,11-dihydroxy-2,5,10a,12a-tetramethyl-7-phenyl-1,2,3,3a,3b,7,10,10a,10b,11,12,12a-dodecahydrocyclopenta[5,6]naphtho[1,2-f]indazol-1-yl]-2-hydroxyethanone, Glucocorticoid receptor, Nuclear receptor coactivator 1
著者Xu, H.E.
登録日2007-12-20
公開日2008-01-15
最終更新日2023-08-30
実験手法X-RAY DIFFRACTION (2.5 Å)
主引用文献Doubling the size of the glucocorticoid receptor ligand binding pocket by deacylcortivazol.
Mol.Cell.Biol., 28, 2008
7KZL
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Cyclopentane peptide nucleic acid in complex with DNA
分子名称: 1,2-ETHANEDIOL, DNA (5'-D(*TP*AP*TP*CP*AP*CP*AP*TP*C)-3'), IODIDE ION, ...
著者Botos, I, Appella, D.H.
登録日2020-12-10
公開日2020-12-23
最終更新日2024-04-03
実験手法X-RAY DIFFRACTION (1.3 Å)
主引用文献Conformational constraints of cyclopentane peptide nucleic acids facilitate tunable binding to DNA.
Nucleic Acids Res., 49, 2021
1E3M
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The crystal structure of E. coli MutS binding to DNA with a G:T mismatch
分子名称: 5'-D(*AP*GP*CP*TP*GP*CP*CP*AP*GP*GP*CP*AP*CP*CP*AP* GP*TP*GP*TP*CP*AP*GP*CP*GP*TP*CP*CP*TP*AP*T)-3', 5'-D(*AP*TP*AP*GP*GP*AP*CP*GP*CP*TP*GP*AP*CP*AP*CP* TP*GP*GP*TP*GP*CP*TP*TP*GP*GP*CP*AP*GP*CP*T)-3', ADENOSINE-5'-DIPHOSPHATE, ...
著者Lamers, M.H, Perrakis, A, Enzlin, J.H, Winterwerp, H.H.K, De Wind, N, Sixma, T.K.
登録日2000-06-19
公開日2000-11-01
最終更新日2017-07-05
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献The Crystal Structure of DNA Mismatch Repair Protein Muts Binding to a G X T Mismatch
Nature, 407, 2000
1D2N
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D2 DOMAIN OF N-ETHYLMALEIMIDE-SENSITIVE FUSION PROTEIN
分子名称: GLYCEROL, MAGNESIUM ION, N-ETHYLMALEIMIDE-SENSITIVE FUSION PROTEIN, ...
著者Lenzen, C.U, Steinmann, D, Whiteheart, S.W, Weis, W.I.
登録日1998-06-30
公開日1998-10-14
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (1.75 Å)
主引用文献Crystal structure of the hexamerization domain of N-ethylmaleimide-sensitive fusion protein.
Cell(Cambridge,Mass.), 94, 1998
1G63
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PEPTIDYL-CYSTEINE DECARBOXYLASE EPID
分子名称: EPIDERMIN MODIFYING ENZYME EPID, FLAVIN MONONUCLEOTIDE
著者Blaesse, M, Kupke, T, Huber, R, Steinbac, S.
登録日2000-11-03
公開日2001-05-03
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (2.5 Å)
主引用文献Crystal structure of the peptidyl-cysteine decarboxylase EpiD complexed with a pentapeptide substrate.
EMBO J., 19, 2000
1G5Q
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EPID H67N COMPLEXED WITH SUBSTRATE PEPTIDE DSYTC
分子名称: 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, EPIDERMIN MODIFYING ENZYME EPID, FLAVIN MONONUCLEOTIDE, ...
著者Blaesse, M, Kupke, T, Huber, R, Steinbacher, S.
登録日2000-11-02
公開日2001-05-02
最終更新日2024-04-03
実験手法X-RAY DIFFRACTION (2.57 Å)
主引用文献Crystal structure of the peptidyl-cysteine decarboxylase EpiD complexed with a pentapeptide substrate.
EMBO J., 19, 2000
8IJK
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human KCNQ2-CaM-Ebio1 complex in the presence of PIP2
分子名称: Calmodulin-1, N-(1,2-dihydroacenaphthylen-5-yl)-4-fluoranyl-benzamide, Potassium voltage-gated channel subfamily KQT member 2
著者Ma, D, Guo, J.
登録日2023-02-27
公開日2024-01-17
最終更新日2024-07-10
実験手法ELECTRON MICROSCOPY (3.4 Å)
主引用文献A small-molecule activation mechanism that directly opens the KCNQ2 channel.
Nat.Chem.Biol., 20, 2024
1B4Y
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STRUCTURE AND MECHANISM OF FORMATION OF THE H-Y5 ISOMER OF AN INTRAMOLECULAR DNA TRIPLE HELIX.
分子名称: DNA (H-Y5 TRIPLE HELIX)
著者Van Dongen, M.J.P, Doreleijers, J.F, Van Der Marel, G.A, Van Boom, J.H, Hilbers, C.W, Wijmenga, S.S.
登録日1998-12-30
公開日1999-09-13
最終更新日2023-12-27
実験手法SOLUTION NMR
主引用文献Structure and mechanism of formation of the H-y5 isomer of an intramolecular DNA triple helix.
Nat.Struct.Biol., 6, 1999
1B4I
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Control of K+ Channel Gating by protein phosphorylation: structural switches of the inactivation gate, NMR, 22 structures
分子名称: POTASSIUM CHANNEL
著者Antz, C, Bauer, T, Kalbacher, H, Frank, R, Covarrubias, M, Kalbitzer, H.R, Ruppersberg, J.P, Baukrowitz, T, Fakler, B.
登録日1998-12-22
公開日1999-04-27
最終更新日2022-03-23
実験手法SOLUTION NMR
主引用文献Control of K+ channel gating by protein phosphorylation: structural switches of the inactivation gate.
Nat.Struct.Biol., 6, 1999
8JV7
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Cryo-EM structure of the panda P2X7 receptor in complex with PPADS
分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose, 4-[(E)-[4-methanoyl-6-methyl-5-oxidanyl-3-(phosphonooxymethyl)pyridin-2-yl]diazenyl]benzene-1,3-disulfonic acid, P2X purinoceptor
著者Sheng, D, Hattori, M.
登録日2023-06-27
公開日2023-11-29
最終更新日2024-05-15
実験手法ELECTRON MICROSCOPY (3.6 Å)
主引用文献Structural insights into the orthosteric inhibition of P2X receptors by non-ATP analog antagonists.
Elife, 12, 2024
8JV8
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Cryo-EM structure of the panda P2X7 receptor in complex with PPNDS
分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose, 3-[(E)-{4-formyl-5-hydroxy-6-methyl-3-[(phosphonooxy)methyl]pyridin-2-yl}diazenyl]-7-nitronaphthalene-1,5-disulfonic acid, P2X purinoceptor
著者Sheng, D, Hattori, M.
登録日2023-06-27
公開日2023-11-29
最終更新日2024-05-15
実験手法ELECTRON MICROSCOPY (3.34 Å)
主引用文献Structural insights into the orthosteric inhibition of P2X receptors by non-ATP analog antagonists.
Elife, 12, 2024
1B4G
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CONTROL OF K+ CHANNEL GATING BY PROTEIN PHOSPHORYLATION: STRUCTURAL SWITCHES OF THE INACTIVATION GATE, NMR, 22 STRUCTURES
分子名称: POTASSIUM CHANNEL
著者Antz, C, Bauer, T, Kalbacher, H, Frank, R, Covarrubias, M, Kalbitzer, H.R, Ruppersberg, J.P, Baukrowitz, T, Fakler, B.
登録日1998-12-22
公開日1999-04-27
最終更新日2022-02-16
実験手法SOLUTION NMR
主引用文献Control of K+ channel gating by protein phosphorylation: structural switches of the inactivation gate.
Nat.Struct.Biol., 6, 1999
7VJT
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Crystal Structure of Mtb Pks13-TE in complex with inhibitor coumestan derivative 8
分子名称: 3,8-bis(oxidanyl)-7-(piperidin-1-ylmethyl)-[1]benzofuro[3,2-c]chromen-6-one, Polyketide synthase Pks13 (Termination polyketide synthase)
著者Zhang, W, Wang, S.S, Yu, L.F.
登録日2021-09-28
公開日2022-09-28
最終更新日2023-11-29
実験手法X-RAY DIFFRACTION (1.94 Å)
主引用文献Structure-Based Optimization of Coumestan Derivatives as Polyketide Synthase 13-Thioesterase(Pks13-TE) Inhibitors with Improved hERG Profiles for Mycobacterium tuberculosis Treatment.
J.Med.Chem., 65, 2022

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件を2024-08-07に公開中

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