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PDB: 46375 件

8TOP
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BU of 8top by Molmil
Cryo-EM structure of HIV-1 Env BG505 DS-SOSIP in complex with antibody GPZ6-b.01 targeting the fusion peptide
分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, HIV-1 BG505 DS-SOSIP glycoprotein gp41, ...
著者Zhou, T, Morano, N.C, Roark, R.S, Kwong, P.D.
登録日2023-08-03
公開日2024-08-07
実験手法ELECTRON MICROSCOPY (3.52 Å)
主引用文献Cryo-EM structure of HIV-1 Env BG505 DS-SOSIP in complex with antibody GPZ6-b.01 targeting the fusion peptide
To Be Published
3ONJ
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BU of 3onj by Molmil
Crystal structure of yeast Vti1p_Habc domain
分子名称: t-SNARE VTI1
著者Wang, J, Fang, P, Niu, L, Teng, M.
登録日2010-08-29
公開日2011-07-20
最終更新日2023-11-01
実験手法X-RAY DIFFRACTION (1.92 Å)
主引用文献Epsin N-terminal homology domains bind on opposite sides of two SNAREs
Proc.Natl.Acad.Sci.USA, 108, 2011
5MVC
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BU of 5mvc by Molmil
Crystal structure of potent human Dihydroorotate Dehydrogenase inhibitors based on hydroxylated azole scaffolds
分子名称: 4-oxidanyl-~{N}-[2,3,5,6-tetrakis(fluoranyl)-4-phenyl-phenyl]-1,2,5-thiadiazole-3-carboxamide, ACETATE ION, CHLORIDE ION, ...
著者Goyal, P, Andersson, M, Moritzer, A.C, Sainas, S, Pippione, A.C, Boschi, D, Al-Kadaraghi, S, Lolli, M, Friemann, R.
登録日2017-01-16
公開日2017-03-08
最終更新日2024-01-17
実験手法X-RAY DIFFRACTION (1.85 Å)
主引用文献Design, synthesis, biological evaluation and X-ray structural studies of potent human dihydroorotate dehydrogenase inhibitors based on hydroxylated azole scaffolds.
Eur J Med Chem, 129, 2017
2W4B
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BU of 2w4b by Molmil
Epstein-Barr virus alkaline nuclease D203S mutant
分子名称: ALKALINE EXONUCLEASE
著者Buisson, M, Geoui, T, Flot, D, Tarbouriech, N, Burmeister, W.P.
登録日2008-11-24
公開日2009-06-30
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (3.5 Å)
主引用文献A Bridge Crosses the Active Site Canyon of the Epstein-Barr Virus Nuclease with DNase and Rnase Activity.
J.Mol.Biol., 391, 2009
8TO7
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BU of 8to7 by Molmil
Cryo-EM structure of HERH-b*01 Fab in complex with HIV-1 Env trimer BG505.DS SOSIP
分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, HERH-b*01 heavy chain, ...
著者Roark, R.S, Hoyt, F, Hansen, B, Fischer, E, Shapiro, L.S, Kwong, P.D.
登録日2023-08-03
公開日2024-08-07
実験手法ELECTRON MICROSCOPY (3.39 Å)
主引用文献Broad and potent HIV-1 neutralization in fusion peptide-primed SHIV-boosted macaques
To Be Published
3P5N
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BU of 3p5n by Molmil
Structure and mechanism of the S component of a bacterial ECF transporter
分子名称: RIBOFLAVIN, Riboflavin uptake protein
著者Zhang, P, Wang, J, Shi, Y.
登録日2010-10-09
公開日2010-11-03
最終更新日2024-03-20
実験手法X-RAY DIFFRACTION (3.6 Å)
主引用文献Structure and mechanism of the S component of a bacterial ECF transporter
Nature, 468, 2010
8TO9
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BU of 8to9 by Molmil
Cryo-EM structure of TRNM-f*01 Fab in complex with HIV-1 Env trimer ConC SOSIP
分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, Envelope glycoprotein gp120, ...
著者Roark, R.S, Morano, N.C, Shapiro, L.S, Kwong, P.D.
登録日2023-08-03
公開日2024-08-07
実験手法ELECTRON MICROSCOPY (4.03 Å)
主引用文献Broad and potent HIV-1 neutralization in fusion peptide-primed SHIV-boosted macaques
To Be Published
2W1I
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BU of 2w1i by Molmil
Structure determination of Aurora Kinase in complex with inhibitor
分子名称: 4-[(2-{4-[(CYCLOPROPYLCARBAMOYL)AMINO]-1H-PYRAZOL-3-YL}-1H-BENZIMIDAZOL-6-YL)METHYL]MORPHOLIN-4-IUM, JAK2
著者Howard, S, Berdini, V, Boulstridge, J.A, Carr, M.G, Cross, D.M, Curry, J, Devine, L.A, Early, T.R, Fazal, L, Gill, A.L, Heathcote, M, Maman, S, Matthews, J.E, McMenamin, R.L, Navarro, E.F, O'Brien, M.A, O'Reilly, M, Rees, D.C, Reule, M, Tisi, D, Williams, G, Vinkovic, M, Wyatt, P.G.
登録日2008-10-17
公開日2009-01-27
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (2.6 Å)
主引用文献Fragment-Based Discovery of the Pyrazol-4-Yl Urea (at9283), a Multitargeted Kinase Inhibitor with Potent Aurora Kinase Activity.
J.Med.Chem., 52, 2009
7XLY
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BU of 7xly by Molmil
Crystal structure of FadA2 (Rv0243) from the fatty acid metabolic pathway of Mycobacterium tuberculosis
分子名称: Probable acetyl-CoA acyltransferase FadA2 (3-ketoacyl-CoA thiolase) (Beta-ketothiolase), SULFATE ION
著者Singh, R, Kundu, P, Singh, B.K, Bhattacharyya, S, Das, A.K.
登録日2022-04-23
公開日2023-04-26
最終更新日2023-08-30
実験手法X-RAY DIFFRACTION (2.9 Å)
主引用文献Crystal structure of FadA2 thiolase from Mycobacterium tuberculosis and prediction of its substrate specificity and membrane-anchoring properties.
Febs J., 290, 2023
2W7W
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BU of 2w7w by Molmil
The crystal structure of iron superoxide dismutase from Aliivibrio salmonicida.
分子名称: FE (III) ION, SUPEROXIDE DISMUTASE [FE]
著者Pedersen, H.L, Willassen, N.P, Leiros, I.
登録日2009-01-06
公開日2009-02-17
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (1.7 Å)
主引用文献The first structure of a cold-adapted superoxide dismutase (SOD): biochemical and structural characterization of iron SOD from Aliivibrio salmonicida.
Acta Crystallogr. Sect. F Struct. Biol. Cryst. Commun., 65, 2009
2WA7
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BU of 2wa7 by Molmil
Structure of the M202V mutant of human filamin b actin binding domain at 1.85 Angstrom resolution
分子名称: CACODYLATE ION, CARBONATE ION, FILAMIN-B
著者Sawyer, G.M, Clark, A.R, Robertson, S.P, Sutherland-Smith, A.J.
登録日2009-02-03
公開日2009-06-23
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (1.85 Å)
主引用文献Disease-Associated Substitutions in the Filamin B Actin Binding Domain Confer Enhanced Actin Binding Affinity in the Absence of Major Structural Disturbance: Insights from the Crystal Structures of Filamin B Actin Binding Domains.
J.Mol.Biol., 390, 2009
8TK4
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BU of 8tk4 by Molmil
HUMAN VH1-RELATED DUAL-SPECIFICITY PHOSPHATASE (VHR) complexed with phosphate
分子名称: Dual specificity protein phosphatase 3, PHOSPHATE ION
著者Aleshin, A.E, Wu, J, Lambert, L.J, Cosford, N.D.P, Tautz, L.
登録日2023-07-25
公開日2024-08-14
実験手法X-RAY DIFFRACTION (1.8 Å)
主引用文献HUMAN VH1-RELATED DUAL-SPECIFICITY PHOSPHATASE (VHR) complexed with phosphate
To Be Published
3P9C
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BU of 3p9c by Molmil
Crystal structure of perennial ryegrass LpOMT1 bound to SAH
分子名称: (2S,3S)-1,4-DIMERCAPTOBUTANE-2,3-DIOL, 1,2-ETHANEDIOL, ACETATE ION, ...
著者Louie, G.V, Noel, J.P, Bowman, M.E.
登録日2010-10-17
公開日2011-01-12
最終更新日2023-09-06
実験手法X-RAY DIFFRACTION (1.8 Å)
主引用文献Structure-Function Analyses of a Caffeic Acid O-Methyltransferase from Perennial Ryegrass Reveal the Molecular Basis for Substrate Preference.
Plant Cell, 22, 2010
8TOX
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BU of 8tox by Molmil
Cryo-EM structure of BG505 Env mutant A517E in complex with antibody ACS202 Fab
分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, Envelope glycoprotein gp120, ...
著者Wang, S, Kwong, P.D.
登録日2023-08-04
公開日2024-08-14
実験手法ELECTRON MICROSCOPY (2.3 Å)
主引用文献Cryo-EM structure of BG505 Env mutant A517E in complex with antibody ACS202 Fab
To Be Published
2WAS
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BU of 2was by Molmil
Structure of the fungal type I FAS PPT domain
分子名称: 3-OXOACYL-[ACYL-CARRIER-PROTEIN] SYNTHASE
著者Johansson, P, Mulincacci, B, Koestler, C, Grininger, M.
登録日2009-02-15
公開日2009-08-25
最終更新日2024-05-08
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献Multimeric Options for the Auto-Activation of the Saccharomyces Cerevisiae Fas Type I Megasynthase.
Structure, 17, 2009
8TGW
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BU of 8tgw by Molmil
Cryo-EM structure of 1059 SOSIP trimer purified via Galanthus nivalis lectin chromatography
分子名称: 1059 SOSIP Surface protein gp120, 1059 SOSIP Transmembrane protein gp41, 2-acetamido-2-deoxy-beta-D-glucopyranose, ...
著者Parsons, R.J, Pothula, K, Acharya, P.
登録日2023-07-13
公開日2024-08-28
最終更新日2024-10-09
実験手法ELECTRON MICROSCOPY (3.6 Å)
主引用文献Conformational flexibility of HIV-1 envelope glycoproteins modulates transmitted/founder sensitivity to broadly neutralizing antibodies.
Nat Commun, 15, 2024
2WFW
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BU of 2wfw by Molmil
Structure and activity of the N-terminal substrate recognition domains in proteasomal ATPases - The Arc domain structure
分子名称: ARC
著者Djuranovic, S, Hartmann, M.D, Habeck, M, Ursinus, A, Zwickl, P, Martin, J, Lupas, A.N, Zeth, K.
登録日2009-04-15
公開日2009-05-12
最終更新日2024-05-08
実験手法X-RAY DIFFRACTION (1.6 Å)
主引用文献Structure and Activity of the N-Terminal Substrate Recognition Domains in Proteasomal Atpases.
Mol.Cell, 34, 2009
3OHW
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BU of 3ohw by Molmil
X-Ray Structure of Phycobilisome LCM core-membrane linker polypeptide (fragment 721-860) from Synechocystis sp. PCC 6803, Northeast Structural Genomics Consortium Target SgR209E
分子名称: Phycobilisome LCM core-membrane linker polypeptide
著者Kuzin, A, Su, M, Lew, S, Vorobiev, S.M, Patel, P, Xiao, R, Ciccosanti, C, Lee, D, Everett, J.K, Nair, R, Acton, T.B, Rost, B, Montelione, G.T, Hunt, J.F, Tong, L, Northeast Structural Genomics Consortium (NESG)
登録日2010-08-18
公開日2010-09-01
最終更新日2024-10-16
実験手法X-RAY DIFFRACTION (2.7 Å)
主引用文献Northeast Structural Genomics Consortium Target SgR209E
To be Published
5JR8
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BU of 5jr8 by Molmil
Disposal of Iron by a Mutant form of Siderocalin NGAL
分子名称: GLYCEROL, Neutrophil gelatinase-associated lipocalin, PHOSPHATE ION
著者Rupert, P.B, Strong, R.K, Barasch, J, Hollman, M, Deng, R, Hod, E.A, Abergel, R, Allred, B, Xu, K, Darrah, S, Tekabe, Y, Perlstein, A, Bruck, E, Stauber, J, Corbin, K, Buchen, C, Slavkovich, V, Graziano, J, Spitalnik, S, Qiu, A.
登録日2016-05-05
公開日2016-09-28
最終更新日2023-09-27
実験手法X-RAY DIFFRACTION (2.65 Å)
主引用文献Disposal of iron by a mutant form of lipocalin 2.
Nat Commun, 7, 2016
8TGU
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BU of 8tgu by Molmil
Cryo-EM structure of BG505 SOSIP trimer purified via Galanthus nivalis lectin chromatography
分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, HIV-1 Envelope glycoprotein BG505 SOSIP, ...
著者Parsons, R.J, Pothula, K, Acharya, P.
登録日2023-07-13
公開日2024-08-28
最終更新日2024-09-04
実験手法ELECTRON MICROSCOPY (3.8 Å)
主引用文献Conformational flexibility of HIV-1 envelope glycoproteins modulates transmitted/founder sensitivity to broadly neutralizing antibodies.
Nat Commun, 15, 2024
6SZ8
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BU of 6sz8 by Molmil
Crystal structure of YTHDC1 with fragment 6 (DHU_DC1_034)
分子名称: 6-pyrrolidin-1-yl-5~{H}-pyrimidine-2,4-dione, SULFATE ION, YTH domain-containing protein 1
著者Bedi, R.K, Huang, D, Sledz, P, Caflisch, A.
登録日2019-10-02
公開日2020-03-04
最終更新日2024-01-24
実験手法X-RAY DIFFRACTION (1.47 Å)
主引用文献Selectively Disrupting m6A-Dependent Protein-RNA Interactions with Fragments.
Acs Chem.Biol., 15, 2020
2VQX
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BU of 2vqx by Molmil
Precursor of Protealysin, Metalloproteinase from Serratia proteamaculans.
分子名称: METALLOPROTEINASE, ZINC ION
著者Melik-Adamyan, W.R, Kuranova, I.P, Polyakov, K.M, Demidyuk, I.V, Gromova, T.Y, Kostrov, S.V.
登録日2008-03-20
公開日2009-05-26
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (1.821 Å)
主引用文献Crystal Structure of the Protealysin Precursor: Insights Into Propeptide Function.
J.Biol.Chem., 285, 2010
6SZN
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Crystal structure of YTHDC1 with fragment 8 (DHU_DC1_006)
分子名称: N-carbamoylbenzamide, SULFATE ION, YTH domain-containing protein 1
著者Bedi, R.K, Huang, D, Sledz, P, Caflisch, A.
登録日2019-10-02
公開日2020-03-04
最終更新日2024-01-24
実験手法X-RAY DIFFRACTION (1.47 Å)
主引用文献Selectively Disrupting m6A-Dependent Protein-RNA Interactions with Fragments.
Acs Chem.Biol., 15, 2020
6WVT
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BU of 6wvt by Molmil
Structural basis of alphaE-catenin - F-actin catch bond behavior
分子名称: ADENOSINE-5'-DIPHOSPHATE, Actin, alpha skeletal muscle, ...
著者Xu, X.P, Pokutta, S, Torres, M, Swift, M.F, Hanein, D, Volkmann, N, Weis, W.I.
登録日2020-05-06
公開日2020-10-07
実験手法ELECTRON MICROSCOPY (3.56 Å)
主引用文献Structural basis of alpha E-catenin-F-actin catch bond behavior.
Elife, 9, 2020
3OMU
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BU of 3omu by Molmil
Crystal Structure of the N-terminal domain of an HSP90 from Trypanosoma Brucei, Tb10.26.1080 in the presence of a thienopyrimidine derivative
分子名称: 2-amino-4-{2,4-dichloro-5-[2-(diethylamino)ethoxy]phenyl}-N-ethylthieno[2,3-d]pyrimidine-6-carboxamide, Heat shock protein 83
著者Wernimont, A.K, Hutchinson, A, Sullivan, H, Weadge, J, Cossar, D, Li, Y, Kozieradzki, I, Bochkarev, A, Arrowsmith, C.H, Edwards, A.M, Bountra, C, Weigelt, J, Wyatt, P.G, Fairlamb, A.H, MacKenzie, C, Ferguson, M.A.J, Hui, R, Pizarro, J.C, Hills, T, Structural Genomics Consortium (SGC)
登録日2010-08-27
公開日2010-10-27
最終更新日2024-10-16
実験手法X-RAY DIFFRACTION (2.15 Å)
主引用文献Exploring the Trypanosoma brucei Hsp83 potential as a target for structure guided drug design.
PLoS Negl Trop Dis, 7, 2013

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