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6INK
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BU of 6ink by Molmil
Crystal structure of PDE4D complexed with a novel inhibitor
分子名称: (1S)-1-[2-(1H-indol-3-yl)ethyl]-6,7-dimethoxy-3,4-dihydroisoquinoline-2(1H)-carbaldehyde, 1,2-ETHANEDIOL, MAGNESIUM ION, ...
著者Zhang, X.L, Su, H.X, Xu, Y.C.
登録日2018-10-25
公開日2019-10-23
最終更新日2024-03-27
実験手法X-RAY DIFFRACTION (1.7 Å)
主引用文献Structure-Aided Identification and Optimization of Tetrahydro-isoquinolines as Novel PDE4 Inhibitors Leading to Discovery of an Effective Antipsoriasis Agent.
J.Med.Chem., 62, 2019
8JB5
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BU of 8jb5 by Molmil
The cryo-EM structure of Paeniclostridium sordellii lethal toxin (TcsL)
分子名称: Cytotoxin-L, ZINC ION
著者Zhan, X, Tao, L.
登録日2023-05-08
公開日2023-12-13
最終更新日2023-12-20
実験手法ELECTRON MICROSCOPY (2.9 Å)
主引用文献Structural dynamics of CROPs control stability and toxicity of Paeniclostridium sordellii lethal toxin
Nat Commun, 2023
8X2I
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BU of 8x2i by Molmil
Cryo-EM structure of the TcsL at pH 5.0 in its open conformation
分子名称: Cytotoxin-L, ZINC ION
著者Zhan, X, Tao, L.
登録日2023-11-09
公開日2023-12-13
実験手法ELECTRON MICROSCOPY (2.5 Å)
主引用文献Structural dynamics of CROPs control stability and toxicity of Paeniclostridium sordellii lethal toxin
Nat Commun, 2023
8X2H
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BU of 8x2h by Molmil
Cryo-EM structure of the TcsL at pH 5.0 in its closed conformation
分子名称: Cytotoxin-L, ZINC ION
著者Zhan, X, Tao, L.
登録日2023-11-09
公開日2023-12-13
実験手法ELECTRON MICROSCOPY (2.9 Å)
主引用文献Structural dynamics of CROPs control stability and toxicity of Paeniclostridium sordellii lethal toxin
Nat Commun, 2023
9M3U
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BU of 9m3u by Molmil
Crystal structure of human pyruvate dehydrogenase kinase isoform 2 in complex with ATP competitive inhibitor 24
分子名称: 1,2-ETHANEDIOL, 2-cyano-N-[(3R)-1-[(3S)-3-ethyl-7-(ethylamino)-5-fluoranyl-2-oxidanylidene-1H-indol-3-yl]piperidin-3-yl]-2-azaspiro[3.3]heptane-6-carboxamide, GLYCEROL, ...
著者Xu, Z.H, Chen, S, Han, L.
登録日2025-03-03
公開日2025-06-25
実験手法X-RAY DIFFRACTION (1.92 Å)
主引用文献Discovery of ATP competitive PDHK1/2 dual inhibitors.
Bioorg.Med.Chem.Lett., 122, 2025
9M3R
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BU of 9m3r by Molmil
Crystal structure of human pyruvate dehydrogenase kinase isoform 1 in complex with ATP competitive inhibitor 29
分子名称: 1,2-ETHANEDIOL, 3-[4-[4-(ethylamino)-6-fluoranyl-2-oxidanylidene-3H-benzimidazol-1-yl]phenoxy]benzenesulfonyl fluoride, GLYCEROL, ...
著者Xu, Z.H, Chen, S.
登録日2025-03-03
公開日2025-06-25
実験手法X-RAY DIFFRACTION (2.14 Å)
主引用文献Discovery of ATP competitive PDHK1/2 dual inhibitors.
Bioorg.Med.Chem.Lett., 122, 2025
9M3T
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BU of 9m3t by Molmil
Crystal structure of human pyruvate dehydrogenase kinase isoform 2 in complex with ATP competitive inhibitor 22
分子名称: 2-chloranyl-4-[[(3R)-1-[(3S)-7-(ethylamino)-5-fluoranyl-3-methyl-2-oxidanylidene-1H-indol-3-yl]piperidin-3-yl]amino]benzoic acid, DIMETHYL SULFOXIDE, N-(2-AMINOETHYL)-2-{3-CHLORO-4-[(4-ISOPROPYLBENZYL)OXY]PHENYL} ACETAMIDE, ...
著者Xu, Z.H, Chen, S.
登録日2025-03-03
公開日2025-06-11
実験手法X-RAY DIFFRACTION (2.08 Å)
主引用文献Discovery of ATP competitive PDHK1/2 dual inhibitors.
Bioorg.Med.Chem.Lett., 122, 2025
9M3O
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BU of 9m3o by Molmil
Crystal structure of human pyruvate dehydrogenase kinase isoform 1 in complex with ATP competitive inhibitor 8
分子名称: 6-fluoranyl-8-(methylamino)-N-(pyrimidin-5-ylmethyl)-9H-pyrido[2,3-b]indole-3-carboxamide, GLYCEROL, POTASSIUM ION, ...
著者Xu, Z.H, Chen, S.
登録日2025-03-03
公開日2025-04-02
実験手法X-RAY DIFFRACTION (1.762 Å)
主引用文献Discovery of ATP competitive PDHK1/2 dual inhibitors.
Bioorg.Med.Chem.Lett., 122, 2025
9M3P
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BU of 9m3p by Molmil
Crystal structure of human pyruvate dehydrogenase kinase isoform 1 in complex with ATP competitive inhibitor 3
分子名称: GLYCEROL, N-[4-(2-chloro-5-methylpyrimidin-4-yl)phenyl]-N-(4-{[(difluoroacetyl)amino]methyl}benzyl)-2,4-dihydroxybenzamide, POTASSIUM ION, ...
著者Xu, Z.H, Chen, S.
登録日2025-03-03
公開日2025-04-02
実験手法X-RAY DIFFRACTION (2.01 Å)
主引用文献Discovery of ATP competitive PDHK1/2 dual inhibitors.
Bioorg.Med.Chem.Lett., 122, 2025
9LHJ
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BU of 9lhj by Molmil
UBE2N/UBE2V2 complexed with a covalent inhibitor
分子名称: Ubiquitin-conjugating enzyme E2 N, Ubiquitin-conjugating enzyme E2 variant 2
著者Li, S, Wu, X, Zhou, L, Lu, X.
登録日2025-01-12
公開日2025-05-14
最終更新日2025-06-25
実験手法X-RAY DIFFRACTION (1.68 Å)
主引用文献Proteome-Wide Data Guides the Discovery of Lysine-Targeting Covalent Inhibitors Using DNA-Encoded Chemical Libraries.
Angew.Chem.Int.Ed.Engl., 64, 2025
9LG2
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BU of 9lg2 by Molmil
Phosphoglycerate mutase 1 complexed with a covalent inhibitor
分子名称: CHLORIDE ION, Phosphoglycerate mutase 1
著者Li, S, Wu, X, Zhou, L, Lu, X.
登録日2025-01-09
公開日2025-05-14
最終更新日2025-06-25
実験手法X-RAY DIFFRACTION (2.02 Å)
主引用文献Proteome-Wide Data Guides the Discovery of Lysine-Targeting Covalent Inhibitors Using DNA-Encoded Chemical Libraries.
Angew.Chem.Int.Ed.Engl., 64, 2025
9LVG
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BU of 9lvg by Molmil
Crystal structure of the mouse RIP3 kinase domain in complexed with Robinetin
分子名称: 3,7-bis(oxidanyl)-2-[3,4,5-tris(oxidanyl)phenyl]chromen-4-one, Receptor-interacting serine/threonine-protein kinase 3
著者Xie, H, Su, H.X, Li, M.J, Xu, Y.C.
登録日2025-02-12
公開日2025-05-07
最終更新日2025-05-21
実験手法X-RAY DIFFRACTION (2.03 Å)
主引用文献Identification of RIPK3 as a target of flavonoids for anti-necroptosis in vitro.
Bioorg.Chem., 161, 2025
9LVH
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BU of 9lvh by Molmil
Crystal structure of the mouse RIP3 kinase domain in complexed with Tricetin
分子名称: 5,7-DIHYDROXY-2-(3,4,5-TRIHYDROXYPHENYL)-4H-CHROMEN-4-ONE, Receptor-interacting serine/threonine-protein kinase 3
著者Xie, H, Su, H.X, Li, M.J, Xu, Y.C.
登録日2025-02-12
公開日2025-05-07
最終更新日2025-05-21
実験手法X-RAY DIFFRACTION (2.38 Å)
主引用文献Identification of RIPK3 as a target of flavonoids for anti-necroptosis in vitro.
Bioorg.Chem., 161, 2025
8HRD
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BU of 8hrd by Molmil
Crystal structure of the receptor binding domain of SARS-CoV-2 Delta variant in complex with IMCAS74 Fab and W14 Fab
分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose, IMCAS74 Fab heavy chain, IMCAS74 Fab light chain, ...
著者Zhao, R.C, Wu, L.L, Han, P.
登録日2022-12-15
公開日2023-12-20
最終更新日2024-10-23
実験手法X-RAY DIFFRACTION (2.86 Å)
主引用文献Defining a de novo non-RBM antibody as RBD-8 and its synergistic rescue of immune-evaded antibodies to neutralize Omicron SARS-CoV-2.
Proc.Natl.Acad.Sci.USA, 120, 2023
9L3Z
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BU of 9l3z by Molmil
Cryo-EM structure of the inactive chemokine-like receptor 1 (CMKLR1)
分子名称: Chemerin-like receptor 1,Soluble cytochrome b562, LRH7-C2, The heavy chain of anti-BRIL Fab, ...
著者Zhu, Y, He, M, Wu, B, Zhao, Q.
登録日2024-12-19
公開日2025-03-12
最終更新日2025-06-11
実験手法ELECTRON MICROSCOPY (3.9 Å)
主引用文献Structural insights into the distinct ligand recognition and signaling of the chemerin receptors CMKLR1 and GPR1.
Protein Cell, 16, 2025
9L3W
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BU of 9l3w by Molmil
Cryo-EM structure of the chemokine-like receptor 1 in complex with chemerin and Gi1
分子名称: Chemerin-like receptor 1, Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2, Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, ...
著者Zhu, Y, He, M, Wu, B, Zhao, Q.
登録日2024-12-19
公開日2025-03-12
最終更新日2025-06-11
実験手法ELECTRON MICROSCOPY (3.5 Å)
主引用文献Structural insights into the distinct ligand recognition and signaling of the chemerin receptors CMKLR1 and GPR1.
Protein Cell, 16, 2025
9L3Y
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BU of 9l3y by Molmil
Cryo-EM structure of the G-protein coupled receptor 1 (GPR1) in complex with chemerin and Gi1
分子名称: Chemerin-like receptor 2, Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2, Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, ...
著者Zhu, Y, He, M, Wu, B, Zhao, Q.
登録日2024-12-19
公開日2025-03-12
最終更新日2025-06-11
実験手法ELECTRON MICROSCOPY (3.6 Å)
主引用文献Structural insights into the distinct ligand recognition and signaling of the chemerin receptors CMKLR1 and GPR1.
Protein Cell, 16, 2025
1UEF
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BU of 1uef by Molmil
Crystal Structure of Dok1 PTB Domain Complex
分子名称: 13-mer peptide from Proto-oncogene tyrosine-protein kinase receptor ret, Docking protein 1
著者Shi, N, Ye, S, Liu, Y, Zhou, W, Ding, Y, Lou, Z, Qiang, B, Yan, J, Rao, Z.
登録日2003-05-14
公開日2004-05-25
最終更新日2024-11-13
実験手法X-RAY DIFFRACTION (2.5 Å)
主引用文献Structural Basis for the Specific Recognition of RET by the Dok1 Phosphotyrosine Binding Domain
J.Biol.Chem., 279, 2004
6KV5
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BU of 6kv5 by Molmil
Structure of influenza D virus apo polymerase
分子名称: Polymerase 3, Polymerase PB2, RNA-directed RNA polymerase catalytic subunit
著者Peng, Q, Peng, R, Qi, J, Gao, G.F, Shi, Y.
登録日2019-09-03
公開日2019-10-02
最終更新日2024-03-27
実験手法ELECTRON MICROSCOPY (4.6 Å)
主引用文献Structural insight into RNA synthesis by influenza D polymerase.
Nat Microbiol, 4, 2019
5D8W
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BU of 5d8w by Molmil
Structrue of a lucidum protein
分子名称: Endoglucanase
著者Guo, R, Li, Q, Shang, N, Liu, G, Ko, T.P, Chen, C.C, Liu, W.
登録日2015-08-18
公開日2016-06-29
最終更新日2024-11-06
実験手法X-RAY DIFFRACTION (2.86 Å)
主引用文献Functional and structural analyses of a 1,4-beta-endoglucanase from Ganoderma lucidum.
Enzyme.Microb.Technol., 86, 2016
6KUJ
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BU of 6kuj by Molmil
Structure of influenza D virus polymerase bound to cRNA promoter in class 1
分子名称: 3'-cRNA promoter, 5'-cRNA promoter, Polymerase 3, ...
著者Peng, Q, Peng, R, Qi, J, Gao, G.F, Shi, Y.
登録日2019-09-02
公開日2019-10-02
最終更新日2025-07-02
実験手法ELECTRON MICROSCOPY (3.4 Å)
主引用文献Structure of influenza D virus polymerase bound to cRNA promoter in Mode A conformation
NAT NANOTECHNOL, 2019
4WIV
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BU of 4wiv by Molmil
Crystal Structure of the first bromodomain of human BRD4 in complex with a novel inhibitor UMB32 (N-TERT-BUTYL-2-[4-(3,5-DIMETHYL-1,2-OXAZOL-4-YL) PHENYL]IMIDAZO[1,2-A]PYRAZIN-3-AMINE)
分子名称: 1,2-ETHANEDIOL, Bromodomain-containing protein 4, GLYCEROL, ...
著者Xu, X, Blacklow, S.
登録日2014-09-26
公開日2014-10-29
最終更新日2023-09-27
実験手法X-RAY DIFFRACTION (1.56 Å)
主引用文献Biased multicomponent reactions to develop novel bromodomain inhibitors.
J.Med.Chem., 57, 2014
5DBF
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BU of 5dbf by Molmil
Crystal Structure of Iridoid Synthase from Cantharanthus roseus in complex with NADPH
分子名称: Iridoid synthase, NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE
著者Hu, Y.M, Liu, W.D, Zheng, Y.Y, Xu, Z.X, Ko, T.P, Chen, C.C, Guo, R.T.
登録日2015-08-21
公開日2015-11-04
最終更新日2023-11-08
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Structures of Iridoid Synthase from Cantharanthus roseus with Bound NAD(+) , NADPH, or NAD(+) /10-Oxogeranial: Reaction Mechanisms
Angew.Chem.Int.Ed.Engl., 54, 2015
5DBI
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BU of 5dbi by Molmil
Crystal Structure of Iridoid Synthase from Cantharanthus roseus in complex with NAD+ and 10-oxogeranial
分子名称: (2E,6E)-2,6-dimethylocta-2,6-dienedial, Iridoid synthase, NICOTINAMIDE-ADENINE-DINUCLEOTIDE
著者Hu, Y.M, Liu, W.D, Zheng, Y.Y, Xu, Z.X, Ko, T.P, Chen, C.C, Guo, R.T.
登録日2015-08-21
公開日2015-11-04
最終更新日2023-11-08
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献Structures of Iridoid Synthase from Cantharanthus roseus with Bound NAD(+) , NADPH, or NAD(+) /10-Oxogeranial: Reaction Mechanisms
Angew.Chem.Int.Ed.Engl., 54, 2015
6TI2
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BU of 6ti2 by Molmil
Structure of the Ustilago maydis chorismate mutase 1 in complex with KWL1-b from Zea mays
分子名称: Chromosome 16, whole genome shotgun sequence, Ripening-related protein 3
著者Altegoer, F, Bange, G.
登録日2019-11-21
公開日2020-05-06
最終更新日2024-10-23
実験手法X-RAY DIFFRACTION (2.75 Å)
主引用文献The two paralogous kiwellin proteins KWL1 and KWL1-b from maize are structurally related and have overlapping functions in plant defense.
J.Biol.Chem., 295, 2020

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件を2025-07-09に公開中

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