PDB形式変換不可の PDB エントリー

6TIJ	Structure of A. niger Fdc WT in complex with indol-2-carboxylic acid 分子名称: 1H-indole-2-carboxylic acid, Ferulic acid decarboxylase 1, MANGANESE (II) ION, ... 著者 Leys, D. 登録日 2019-11-22 公開日 2020-06-24 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (1.12 Å) 主引用文献 Enzymatic C-H activation of aromatic compounds through CO 2 fixation. Nat.Chem.Biol., 16, 2020
6TIL	Structure of A. niger Fdc WT in complex with FMN and 2 naphthoic acid 分子名称: FLAVIN MONONUCLEOTIDE, Ferulic acid decarboxylase 1, MANGANESE (II) ION, ... 著者 Leys, D. 登録日 2019-11-22 公開日 2020-06-24 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (1.42 Å) 主引用文献 Enzymatic C-H activation of aromatic compounds through CO 2 fixation. Nat.Chem.Biol., 16, 2020
6TIN	Structure of A. niger Fdc WT in complex with FMN and indole 2 carboxylic acid 分子名称: 1H-indole-2-carboxylic acid, FLAVIN MONONUCLEOTIDE, Ferulic acid decarboxylase 1, ... 著者 Leys, D. 登録日 2019-11-22 公開日 2020-06-24 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (1.28 Å) 主引用文献 Enzymatic C-H activation of aromatic compounds through CO 2 fixation. Nat.Chem.Biol., 16, 2020
6TIO	Structure of A. niger Fdc Wt in complex with FMN and benzothiophene 2 carboxylic acid 分子名称: FLAVIN MONONUCLEOTIDE, Ferulic acid decarboxylase 1, MANGANESE (II) ION, ... 著者 Leys, D. 登録日 2019-11-22 公開日 2020-06-24 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (1.54 Å) 主引用文献 Enzymatic C-H activation of aromatic compounds through CO 2 fixation. Nat.Chem.Biol., 16, 2020
6TIX	Crystal structure of penicillin-binding protein 2 from Yersinia pestis in complex with mecillinam 分子名称: 2-[(1R)-1-{[(E)-azepan-1-ylmethylidene]amino}-2-oxoethyl]-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid, Peptidoglycan D,D-transpeptidase MrdA 著者 Pankov, G, Hunter, W.N, Dawson, A. 登録日 2019-11-22 公開日 2020-12-02 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (2.8 Å) 主引用文献 The structure of penicillin-binding protein 2 from Yersinia pestis in complex with mecillinam To Be Published
6TJJ	Structure of Cerezyme at pH 4.6 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, ACETATE ION, ... 著者 Rowland, R.J, Davies, G.J. 登録日 2019-11-26 公開日 2020-06-10 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (1.59 Å) 主引用文献 A baculoviral system for the production of human beta-glucocerebrosidase enables atomic resolution analysis. Acta Crystallogr D Struct Biol, 76, 2020
6TJK	Crystal Structure of Recombinant GBA in Complex with Bis-Tris Propane. 分子名称: 1,2-ETHANEDIOL, 2-[3-(2-HYDROXY-1,1-DIHYDROXYMETHYL-ETHYLAMINO)-PROPYLAMINO]-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... 著者 Rowland, R.J, Davies, G.J. 登録日 2019-11-26 公開日 2020-06-10 最終更新日 2024-02-07 実験手法 X-RAY DIFFRACTION (1.56 Å) 主引用文献 A baculoviral system for the production of human beta-glucocerebrosidase enables atomic resolution analysis. Acta Crystallogr D Struct Biol, 76, 2020
6TJQ	Crystal Structure of Recombinant GBA in Complex with 2-Deoxy-2-fluoro-beta-D-glucopyranoside 分子名称: (2~{R},3~{S},4~{S},5~{S})-5-fluoranyl-2-(hydroxymethyl)oxane-3,4-diol, 1,2-ETHANEDIOL, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... 著者 Rowland, R.J, Davies, G.J. 登録日 2019-11-26 公開日 2020-06-10 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (1.41 Å) 主引用文献 A baculoviral system for the production of human beta-glucocerebrosidase enables atomic resolution analysis. Acta Crystallogr D Struct Biol, 76, 2020
6TJS	GSTF1 from Alopecurus myosuroides 分子名称: Glutathione transferase 著者 Pohl, E, Eno, R.F.M, Freitag-Pohl, S. 登録日 2019-11-26 公開日 2021-05-12 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (1.53 Å) 主引用文献 GSTF1 from Alopecurus myosuroides To Be Published
6TJU	X-ray structure of C-terminal domain of human T-cell lymphotropic virus type 1 (HTLV-1) 分子名称: Pol protein 著者 Barski, M, Maertens, G.N. 登録日 2019-11-26 公開日 2020-10-21 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (1.8 Å) 主引用文献 Cryo-EM structure of the deltaretroviral intasome in complex with the PP2A regulatory subunit B56 gamma. Nat Commun, 11, 2020
6TK8	GSTF1 F122T variant from Alopecurus myosuroides 分子名称: Glutathione transferase, [(2~{S})-5-[[(2~{R})-1-(2-hydroxy-2-oxoethylamino)-1-oxidanylidene-3-sulfanyl-propan-2-yl]amino]-1-oxidanyl-1,5-bis(oxidanylidene)pentan-2-yl]azanium 著者 Pohl, E, Eno, R.F.M, Freitag-Pohl, S, Steel, P.G. 登録日 2019-11-28 公開日 2021-05-26 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (2.78 Å) 主引用文献 GSTF1 from Alopecurus myosuroides To Be Published
6TKA	Crystal structure of human O-GlcNAc transferase bound to substrate 7 and a peptide from HCF-1 pro-repeat 2 (11-26) 分子名称: 3-[2,2-bis(fluoranyl)-10,12-dimethyl-1,3-diaza-2$l^{4}-boratricyclo[7.3.0.0^{3,7}]dodeca-4,6,9,11-tetraen-4-yl]-~{N}-ethyl-propanamide, HCF-1 pro-repeat 2 (11-26), UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit, ... 著者 Meek, R.W, Davies, G.J. 登録日 2019-11-28 公開日 2020-03-04 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (1.91 Å) 主引用文献 A Direct Fluorescent Activity Assay for Glycosyltransferases Enables Convenient High-Throughput Screening: Application to O-GlcNAc Transferase. Angew.Chem.Int.Ed.Engl., 59, 2020
6TKB	ChiLob 7/4 H2 HC-C224S F(ab')2 分子名称: Chilob 7/4 H2 heavy chain C224S, Chilob 7/4 H2 kappa chain 著者 Orr, C.M, Fisher, H, Tews, I. 登録日 2019-11-28 公開日 2021-06-09 最終更新日 2024-01-31 実験手法 X-RAY DIFFRACTION (2 Å) 主引用文献 Hinge disulfides in human IgG2 CD40 antibodies modulate receptor signaling by regulation of conformation and flexibility. Sci Immunol, 7, 2022
6TKC	ChiLob 7/4 H2 HC-C225S F(ab')2 分子名称: Chilob 7/4 H2 heavy chain C225S, Chilob 7/4 H2 kappa chain 著者 Orr, C.M, Fisher, H, Tews, I. 登録日 2019-11-28 公開日 2021-06-09 最終更新日 2022-12-21 実験手法 X-RAY DIFFRACTION (2.3 Å) 主引用文献 Hinge disulfides in human IgG2 CD40 antibodies modulate receptor signaling by regulation of conformation and flexibility. Sci Immunol, 7, 2022
6TKD	ChiLob 7/4 H2 HC-C228S F(ab')2 分子名称: Chilob 7/4 H2 heavy chain C228S, Chilob 7/4 H2 kappa chain 著者 Orr, C.M, Fisher, H, Tews, I. 登録日 2019-11-28 公開日 2021-06-09 最終更新日 2024-01-31 実験手法 X-RAY DIFFRACTION (1.9 Å) 主引用文献 Hinge disulfides in human IgG2 CD40 antibodies modulate receptor signaling by regulation of conformation and flexibility. Sci Immunol, 7, 2022
6TKE	ChiLob 7/4 H2 HC-C224S Kappa LC-C214S F(ab')2 分子名称: ChiLob 7/4 H2 heavy chain C224S, ChiLob 7/4 H2 kappa chain C214S 著者 Orr, C.M, Fisher, H, Tews, I. 登録日 2019-11-28 公開日 2021-06-09 最終更新日 2024-01-31 実験手法 X-RAY DIFFRACTION (2.35 Å) 主引用文献 Hinge disulfides in human IgG2 CD40 antibodies modulate receptor signaling by regulation of conformation and flexibility. Sci Immunol, 7, 2022
6TKF	ChiLob 7/4 H2 HC-C225S KappaLC-C214S F(ab')2 分子名称: ChiLob 7/4 H2 Heavy chain C225S, ChiLob 7/4 H2 Kappa light chain C214S 著者 Orr, C.M, Fisher, H, Tews, I. 登録日 2019-11-28 公開日 2021-06-09 最終更新日 2024-01-31 実験手法 X-RAY DIFFRACTION (2.18 Å) 主引用文献 Hinge disulfides in human IgG2 CD40 antibodies modulate receptor signaling by regulation of conformation and flexibility. Sci Immunol, 7, 2022
6TKM	Tankyrase 2 in complex with an inhibitor (OM-1800) 分子名称: Tankyrase-2, ZINC ION, ~{N}-[3-[5-(5-ethoxypyridin-2-yl)-4-(2-fluorophenyl)-1,2,4-triazol-3-yl]cyclobutyl]-1,5-naphthyridine-4-carboxamide 著者 Sowa, S.T, Lehtio, L. 登録日 2019-11-28 公開日 2020-07-08 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (2.7 Å) 主引用文献 Preclinical Lead Optimization of a 1,2,4-Triazole Based Tankyrase Inhibitor. J.Med.Chem., 63, 2020
6TKN	Tankyrase 2 in complex with an inhibitor (OM-1000) 分子名称: Tankyrase-2, ZINC ION, ~{N}-[3-[4-(2-chlorophenyl)-5-pyrimidin-4-yl-1,2,4-triazol-3-yl]-1-bicyclo[1.1.1]pentanyl]pyridine-2-carboxamide 著者 Sowa, S.T, Lehtio, L. 登録日 2019-11-28 公開日 2020-07-08 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (2.5 Å) 主引用文献 Preclinical Lead Optimization of a 1,2,4-Triazole Based Tankyrase Inhibitor. J.Med.Chem., 63, 2020
6TKP	Tankyrase 2 in complex with an inhibitor (OM-1900) 分子名称: Tankyrase-2, ZINC ION, ~{N}-[3-[4-(2-chlorophenyl)-5-(5-ethoxypyridin-2-yl)-1,2,4-triazol-3-yl]cyclobutyl]-1,5-naphthyridine-4-carboxamide 著者 Sowa, S.T, Lehtio, L. 登録日 2019-11-28 公開日 2020-07-08 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (2.4 Å) 主引用文献 Preclinical Lead Optimization of a 1,2,4-Triazole Based Tankyrase Inhibitor. J.Med.Chem., 63, 2020
6TKQ	Tankyrase 2 in complex with an inhibitor (OM-2700) 分子名称: Tankyrase-2, ZINC ION, ~{N}-[3-[5-(5-ethoxypyridin-2-yl)-4-phenyl-1,2,4-triazol-3-yl]cyclobutyl]-1,5-naphthyridine-4-carboxamide 著者 Sowa, S.T, Lehtio, L. 登録日 2019-11-28 公開日 2020-07-08 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (2.5 Å) 主引用文献 Preclinical Lead Optimization of a 1,2,4-Triazole Based Tankyrase Inhibitor. J.Med.Chem., 63, 2020
6TKR	Tankyrase 2 in complex with an inhibitor (OM-1704) 分子名称: Tankyrase-2, ZINC ION, ~{N}-[3-[5-(5-ethoxypyridin-2-yl)-4-(2-fluorophenyl)-1,2,4-triazol-3-yl]cyclobutyl]-1,5-naphthyridine-2-carboxamide 著者 Sowa, S.T, Lehtio, L. 登録日 2019-11-28 公開日 2020-07-08 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (2.75 Å) 主引用文献 Preclinical Lead Optimization of a 1,2,4-Triazole Based Tankyrase Inhibitor. J.Med.Chem., 63, 2020
6TKS	Tankyrase 2 in complex with an inhibitor (OM-1720) 分子名称: Tankyrase-2, ZINC ION, ~{N}-[3-[5-(5-ethoxypyridin-2-yl)-4-(2-fluorophenyl)-1,2,4-triazol-3-yl]cyclobutyl]-1,6-naphthyridine-2-carboxamide 著者 Sowa, S.T, Lehtio, L. 登録日 2019-11-28 公開日 2020-07-08 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (2.5 Å) 主引用文献 Preclinical Lead Optimization of a 1,2,4-Triazole Based Tankyrase Inhibitor. J.Med.Chem., 63, 2020
6TKZ	Crystal structure of the DHR2 domain of DOCK10 in complex with CDC42 分子名称: Cell division control protein 42 homolog, Dedicator of cytokinesis protein 10, GLYCEROL, ... 著者 Barford, D. 登録日 2019-11-29 公開日 2020-01-22 最終更新日 2024-01-31 実験手法 X-RAY DIFFRACTION (2.64 Å) 主引用文献 Structural basis for CDC42 and RAC activation by the dual specificity GEF DOCK10 Biorxiv, 2022
6TLU	HUMAN CK2 KINASE ALPHA SUBUNIT IN COMPLEX WITH THE ATP-COMPETITIVE INHIBITOR 4,5-DIBROMOBENZOTRIAZOLE 分子名称: 6,7-bis(bromanyl)-1~{H}-benzotriazole, Casein kinase II subunit alpha, SODIUM ION 著者 Czapinska, H, Piasecka, A, Winiewska-Szajewska, M, Bochtler, M, Poznanski, J. 登録日 2019-12-03 公開日 2020-12-16 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (1.81 Å) 主引用文献 Halogen Atoms in the Protein-Ligand System. Structural and Thermodynamic Studies of the Binding of Bromobenzotriazoles by the Catalytic Subunit of Human Protein Kinase CK2. J.Phys.Chem.B, 125, 2021

<43444546474849505152535455565758>