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PDB: 84 件

1SAY
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L-ALANINE DEHYDROGENASE COMPLEXED WITH PYRUVATE
分子名称: L-ALANINE DEHYDROGENASE, PYRUVIC ACID
著者Baker, P.J, Sawa, Y, Shibata, H, Sedelnikova, S.E, Rice, D.W.
登録日1998-06-05
公開日1999-06-08
最終更新日2023-11-15
実験手法X-RAY DIFFRACTION (2.1 Å)
主引用文献Analysis of the structure and substrate binding of Phormidium lapideum alanine dehydrogenase.
Nat.Struct.Biol., 5, 1998
1PJB
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L-ALANINE DEHYDROGENASE
分子名称: L-ALANINE DEHYDROGENASE
著者Baker, P.J, Sawa, Y, Shibata, H, Sedelnikova, S.E, Rice, D.W.
登録日1998-06-05
公開日1999-06-08
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (2.1 Å)
主引用文献Analysis of the structure and substrate binding of Phormidium lapideum alanine dehydrogenase.
Nat.Struct.Biol., 5, 1998
8U8V
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Cryo-EM structure of Substrate ATP Bound in the Insertion Site (IS) of Human Mitochondrial Transcription Elongation Complex
分子名称: DIPHOSPHOMETHYLPHOSPHONIC ACID ADENOSYL ESTER, DNA-directed RNA polymerase, mitochondrial, ...
著者Herbine, K.H, Nayak, A.R, Temiakov, D.
登録日2023-09-18
公開日2024-09-04
実験手法ELECTRON MICROSCOPY (2.74 Å)
主引用文献Structural basis for substrate binding and selection by human mitochondrial RNA polymerase.
Nat Commun, 15, 2024
8U8U
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Cryo-EM Structure of Cognate Substrate ATP Bound in the Entry Site (ES) of Human Mitochondrial Transcription Elongation Complex
分子名称: DIPHOSPHOMETHYLPHOSPHONIC ACID ADENOSYL ESTER, DNA-directed RNA polymerase, mitochondrial, ...
著者Herbine, K.H, Nayak, A.R, Temiakov, D.
登録日2023-09-18
公開日2024-09-04
実験手法ELECTRON MICROSCOPY (2.9 Å)
主引用文献Structural basis for substrate binding and selection by human mitochondrial RNA polymerase.
Nat Commun, 15, 2024
4YHF
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Bruton's tyrosine kinase in complex with a t-butyl cyanoacrylamide inhibitor
分子名称: (2S)-2-({(3R)-3-[4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]piperidin-1-yl}carbonyl)-4,4-dimethylpentanenitrile, 1,2-ETHANEDIOL, CHLORIDE ION, ...
著者Paavilainen, V.O, McFarland, J.M, Taunton, J.
登録日2015-02-27
公開日2015-05-13
最終更新日2024-11-20
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献Prolonged and tunable residence time using reversible covalent kinase inhibitors.
Nat.Chem.Biol., 11, 2015
7KEF
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RNA polymerase II elongation complex with unnatural base dTPT3, rNaM in swing state
分子名称: (1S)-1,4-anhydro-1-(3-methoxynaphthalen-2-yl)-5-O-phosphono-D-ribitol, DNA-directed RNA polymerase II subunit RPB1, DNA-directed RNA polymerase II subunit RPB11, ...
著者Oh, J, Wang, D.
登録日2020-10-10
公開日2021-06-23
最終更新日2023-10-18
実験手法X-RAY DIFFRACTION (3.89 Å)
主引用文献Transcriptional processing of an unnatural base pair by eukaryotic RNA polymerase II.
Nat.Chem.Biol., 17, 2021
7KED
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RNA polymerase II elongation complex with unnatural base dTPT3
分子名称: DNA-directed RNA polymerase II subunit RPB1, DNA-directed RNA polymerase II subunit RPB11, DNA-directed RNA polymerase II subunit RPB2, ...
著者Oh, J, Wang, W, Wang, D.
登録日2020-10-10
公開日2021-06-23
最終更新日2023-10-18
実験手法X-RAY DIFFRACTION (3.6 Å)
主引用文献Transcriptional processing of an unnatural base pair by eukaryotic RNA polymerase II.
Nat.Chem.Biol., 17, 2021
7KEE
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RNA polymerase II elongation complex with unnatural base dTPT3, rNaMTP bound to E-site
分子名称: (1S)-1,4-anhydro-5-O-[(R)-hydroxy{[(S)-hydroxy(phosphonooxy)phosphoryl]oxy}phosphoryl]-1-(3-methoxynaphthalen-2-yl)-D-ribitol, DNA-directed RNA polymerase II subunit RPB1, DNA-directed RNA polymerase II subunit RPB11, ...
著者Oh, J, Wang, D.
登録日2020-10-10
公開日2021-06-23
最終更新日2023-10-18
実験手法X-RAY DIFFRACTION (3.45 Å)
主引用文献Transcriptional processing of an unnatural base pair by eukaryotic RNA polymerase II.
Nat.Chem.Biol., 17, 2021
7YNX
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Crystal structure of Pirh2 bound to poly-Ala peptide
分子名称: RING finger and CHY zinc finger domain-containing protein 1, SODIUM ION, SULFATE ION, ...
著者Dong, C, Yan, X, Li, Y.
登録日2022-08-01
公開日2023-04-26
最終更新日2024-05-29
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Recognition of an Ala-rich C-degron by the E3 ligase Pirh2.
Nat Commun, 14, 2023
9FX1
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CryoEM structure of RV-A89
分子名称: Capsid protein VP1, Capsid protein VP2, Capsid protein VP3, ...
著者Wald, J, Goessweiner-Mohr, N, Blaas, D, Marlovits, T.C.
登録日2024-07-01
公開日2024-12-18
実験手法ELECTRON MICROSCOPY (1.76 Å)
主引用文献DMSO might impact ligand binding, capsid stability, and RNA interaction in viral preparations.
Sci Rep, 14, 2024
9FX9
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CryoEM structure of RV-A89
分子名称: Capsid protein VP1, Capsid protein VP2, Capsid protein VP3
著者Wald, J, Goessweiner-Mohr, N, Blaas, D, Marlovits, T.C.
登録日2024-07-02
公開日2024-12-18
実験手法ELECTRON MICROSCOPY (1.96 Å)
主引用文献DMSO might impact ligand binding, capsid stability, and RNA interaction in viral preparations.
Sci Rep, 14, 2024
2MXN
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NMR Structure of the mature form of Trypanosoma brucei 1CGrx1
分子名称: Mono-cysteine glutaredoxin
著者Sturlese, M, Bertarello, A, Manta, B, Lelli, M, Mammi, S, Comini, M, Bellanda, M.
登録日2015-01-08
公開日2016-01-27
最終更新日2024-05-01
実験手法SOLUTION NMR
主引用文献The lineage-specific, intrinsically disordered N-terminal extension of monothiol glutaredoxin 1 from trypanosomes contains a regulatory region.
Sci Rep, 8, 2018
4OZH
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S16 protein complex
分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose, CALCIUM ION, Gliadin-alpha2 peptide, ...
著者Petersen, J, Reid, H.H, Rossjohn, J.
登録日2014-02-16
公開日2014-04-16
最終更新日2024-10-23
実験手法X-RAY DIFFRACTION (2.8 Å)
主引用文献T-cell receptor recognition of HLA-DQ2-gliadin complexes associated with celiac disease.
Nat.Struct.Mol.Biol., 21, 2014
4OZF
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JR5.1 protein complex
分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose, HLA class II histocompatibility antigen, DQ alpha 1 chain, ...
著者Petersen, J, Reid, H.H, Rossjohn, J.
登録日2014-02-15
公開日2014-04-16
最終更新日2024-11-20
実験手法X-RAY DIFFRACTION (2.7 Å)
主引用文献T-cell receptor recognition of HLA-DQ2-gliadin complexes associated with celiac disease.
Nat.Struct.Mol.Biol., 21, 2014
4OZI
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S2 protein complex
分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose, CALCIUM ION, HLA class II histocompatibility antigen, ...
著者Petersen, J, Reid, H.H, Rossjohn, J.
登録日2014-02-16
公開日2014-04-16
最終更新日2024-11-06
実験手法X-RAY DIFFRACTION (3.2 Å)
主引用文献T-cell receptor recognition of HLA-DQ2-gliadin complexes associated with celiac disease.
Nat.Struct.Mol.Biol., 21, 2014
4OZG
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D2 protein complex
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, CALCIUM ION, ...
著者Petersen, J, Reid, H.H, Rossjohn, J.
登録日2014-02-16
公開日2014-04-16
最終更新日2024-10-09
実験手法X-RAY DIFFRACTION (3 Å)
主引用文献T-cell receptor recognition of HLA-DQ2-gliadin complexes associated with celiac disease.
Nat.Struct.Mol.Biol., 21, 2014
8UW2
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Structure of AKT1(E17K) with compound 3 (zinc-free)
分子名称: 1,2-ETHANEDIOL, 4-{2-[({4-[(2P)-2-(2-aminopyridin-3-yl)-5-phenyl-3H-imidazo[4,5-b]pyridin-3-yl]phenyl}methyl)amino]ethyl}-2-hydroxybenzaldehyde, NB41, ...
著者Craven, G.B, Taunton, J.
登録日2023-11-05
公開日2024-09-04
最終更新日2025-01-08
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献Mutant-selective AKT inhibition through lysine targeting and neo-zinc chelation.
Nature, 637, 2025
8UW9
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Structure of AKT1(E17K) with compound 4
分子名称: 1,2-ETHANEDIOL, CHLORIDE ION, N-({4-[(2P)-2-(2-aminopyridin-3-yl)-5-phenyl-3H-imidazo[4,5-b]pyridin-3-yl]phenyl}methyl)-2-(2-fluoro-4-formyl-3-hydroxyphenyl)acetamide, ...
著者Craven, G.B, Taunton, J.
登録日2023-11-06
公開日2024-09-04
最終更新日2025-01-08
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献Mutant-selective AKT inhibition through lysine targeting and neo-zinc chelation.
Nature, 637, 2025
8UVY
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Structure of AKT1(E17K) with compound 3
分子名称: 1,2-ETHANEDIOL, 4-{2-[({4-[(2P)-2-(2-aminopyridin-3-yl)-5-phenyl-3H-imidazo[4,5-b]pyridin-3-yl]phenyl}methyl)amino]ethyl}-2-hydroxybenzaldehyde, NB41, ...
著者Craven, G.B, Taunton, J.
登録日2023-11-05
公開日2024-09-04
最終更新日2025-01-08
実験手法X-RAY DIFFRACTION (2.11 Å)
主引用文献Mutant-selective AKT inhibition through lysine targeting and neo-zinc chelation.
Nature, 637, 2025
8UW7
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Structure of AKT1(WT) with compound 3
分子名称: 1,2-ETHANEDIOL, 4-{2-[({4-[(2P)-2-(2-aminopyridin-3-yl)-5-phenyl-3H-imidazo[4,5-b]pyridin-3-yl]phenyl}methyl)amino]ethyl}-2-hydroxybenzaldehyde, NB41, ...
著者Craven, G.B, Taunton, J.
登録日2023-11-06
公開日2024-09-04
最終更新日2025-01-08
実験手法X-RAY DIFFRACTION (1.972 Å)
主引用文献Mutant-selective AKT inhibition through lysine targeting and neo-zinc chelation.
Nature, 637, 2025
7RA8
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SARS-CoV-2 S glycoprotein in complex with S2X259 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, Heavy chain Fab S2X259 Fab variable domain, ...
著者Veesler, D, Tortorici, M.A, Seattle Structural Genomics Center for Infectious Disease (SSGCID)
登録日2021-06-30
公開日2021-08-04
最終更新日2024-10-23
実験手法ELECTRON MICROSCOPY (3.1 Å)
主引用文献Broad sarbecovirus neutralization by a human monoclonal antibody.
Nature, 597, 2021
7RAL
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SARS-CoV-2 S bound to S2X259 Fab (local refinement of the RBD/S2X259 variable domains)
分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose, S2X259 Fab heavy chain, S2X259 Fab light chain, ...
著者Veesler, D, Tortorici, M.A, Seattle Structural Genomics Center for Infectious Disease (SSGCID)
登録日2021-07-01
公開日2021-08-04
最終更新日2025-03-19
実験手法ELECTRON MICROSCOPY (3.7 Å)
主引用文献Broad sarbecovirus neutralization by a human monoclonal antibody.
Nature, 597, 2021
7QHO
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Cytochrome bcc-aa3 supercomplex (respiratory supercomplex III2/IV2) from Corynebacterium glutamicum (as isolated)
分子名称: (2R)-2-(hexadecanoyloxy)-3-{[(S)-hydroxy{[(1R,2R,3R,4R,5R,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxy}phosphoryl]oxy}propyl (9S)-9-methyloctadecanoate, 1,2-DIACYL-GLYCEROL-3-SN-PHOSPHATE, 1,2-Distearoyl-sn-glycerophosphoethanolamine, ...
著者Kao, W.-C, Hunte, C.
登録日2021-12-13
公開日2022-05-18
最終更新日2024-10-23
実験手法ELECTRON MICROSCOPY (3.1 Å)
主引用文献Structural basis for safe and efficient energy conversion in a respiratory supercomplex
Nature Communications, 13, 2022
7QHM
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Cytochrome bcc-aa3 supercomplex (respiratory supercomplex III2/IV2) from Corynebacterium glutamicum (stigmatellin and azide bound)
分子名称: (2R)-2-(hexadecanoyloxy)-3-{[(S)-hydroxy{[(1R,2R,3R,4R,5R,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxy}phosphoryl]oxy}propyl (9S)-9-methyloctadecanoate, 1,2-Distearoyl-sn-glycerophosphoethanolamine, AZIDE ION, ...
著者Kao, W.-C, Hunte, C.
登録日2021-12-13
公開日2022-05-18
最終更新日2024-10-09
実験手法ELECTRON MICROSCOPY (2.8 Å)
主引用文献Structural basis for safe and efficient energy conversion in a respiratory supercomplex.
Nat Commun, 13, 2022
9C1W
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Structure of AKT2 with compound 3
分子名称: 1,2-ETHANEDIOL, 4-{2-[({4-[(2P)-2-(2-aminopyridin-3-yl)-5-phenyl-3H-imidazo[4,5-b]pyridin-3-yl]phenyl}methyl)amino]ethyl}-2-hydroxybenzaldehyde, RAC-beta serine/threonine-protein kinase
著者Craven, G.B, Ma, X, Taunton, J.
登録日2024-05-29
公開日2024-09-04
最終更新日2025-01-08
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Mutant-selective AKT inhibition through lysine targeting and neo-zinc chelation.
Nature, 637, 2025

 

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