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更新された PDB エントリー
9C6Q
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Structure of V. cholerae monomeric DdmD bound with ssDNA
分子名称: Helicase/UvrB N-terminal domain-containing protein, ssDNA
著者Shen, Z.F, Yang, X.Y, Fu, T.M.
登録日2024-06-08
公開日2024-08-21
最終更新日2024-10-02
実験手法ELECTRON MICROSCOPY (3.18 Å)
主引用文献DdmDE eliminates plasmid invasion by DNA-guided DNA targeting.
Cell, 187, 2024
9C6V
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Crystal Structure of a single chain trimer composed of HLA-B*39:06 Y84C variant, beta-2microglobulin, and NRVMLPKAA peptide from NLRP2 (1 molecule/asymmetric unit)
分子名称: 1,2-ETHANEDIOL, CHLORIDE ION, GLYCEROL, ...
著者Sharma, R, Amdare, N.P, Celikgil, A, Garforth, S.J, DiLorenzo, T.P, Almo, S.C, Ghosh, A.
登録日2024-06-09
公開日2024-09-04
最終更新日2024-10-02
実験手法X-RAY DIFFRACTION (1.7 Å)
主引用文献Structural and biochemical analysis of highly similar HLA-B allotypes differentially associated with type 1 diabetes.
J.Biol.Chem., 300, 2024
9C6W
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Crystal Structure of a single chain trimer composed of HLA-B*39:06 Y84C variant, beta-2microglobulin, and NRVMLPKAA peptide from NLRP2 (2 molecules/asymmetric unit)
分子名称: 1,2-ETHANEDIOL, 3,6,9,12,15-PENTAOXAHEPTADECANE, CHLORIDE ION, ...
著者Sharma, R, Amdare, N.P, Celikgil, A, Garforth, S.J, DiLorenzo, T.P, Almo, S.C, Ghosh, A.
登録日2024-06-09
公開日2024-09-04
最終更新日2024-10-02
実験手法X-RAY DIFFRACTION (1.7 Å)
主引用文献Structural and biochemical analysis of highly similar HLA-B allotypes differentially associated with type 1 diabetes.
J.Biol.Chem., 300, 2024
9C6X
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Crystal Structure of a single chain trimer composed of HLA-B*39:01 Y84C variant, beta-2microglobulin, and NRVMLPKAA peptide from NLRP2
分子名称: 1,2-ETHANEDIOL, 1-ETHOXY-2-(2-ETHOXYETHOXY)ETHANE, NACHT, ...
著者Sharma, R, Amdare, N.P, Celikgil, A, Garforth, S.J, DiLorenzo, T.P, Almo, S.C, Ghosh, A.
登録日2024-06-09
公開日2024-09-04
最終更新日2024-10-02
実験手法X-RAY DIFFRACTION (1.7 Å)
主引用文献Structural and biochemical analysis of highly similar HLA-B allotypes differentially associated with type 1 diabetes.
J.Biol.Chem., 300, 2024
9C9V
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HBV capsid with compound 3i
分子名称: Capsid protein, N'-(3-chloro-4-fluorophenyl)-N-(2-methylpropyl)-N-[(1R)-1-(1-oxo-1,2-dihydroisoquinolin-4-yl)ethyl]urea
著者Olland, A.M, Suto, R.K, Fontano, E, Colussi, T.
登録日2024-06-16
公開日2024-09-25
最終更新日2024-10-02
実験手法X-RAY DIFFRACTION (2.63 Å)
主引用文献Rational Design, Synthesis, and Structure-Activity Relationship of a Novel Isoquinolinone-Based Series of HBV Capsid Assembly Modulators Leading to the Identification of Clinical Candidate AB-836.
J.Med.Chem., 67, 2024
9CD5
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FGFR1 Kinase Domain Soak with Inhibitor TYRA-300
分子名称: (3P)-5-[(1R)-1-(3,5-dichloropyridin-4-yl)ethoxy]-3-{6-[6-(methanesulfonyl)-2,6-diazaspiro[3.3]heptan-2-yl]pyridin-3-yl}-1H-indazole, 1,2-ETHANEDIOL, Fibroblast growth factor receptor 1, ...
著者Hoffman, I.H, Nelson, K.J, Rideout, M.C, Frye, C, Bensen, D.C, Hudkins, R.L.
登録日2024-06-24
公開日2024-09-25
最終更新日2024-10-02
実験手法X-RAY DIFFRACTION (2.939 Å)
主引用文献Discovery of TYRA-300: First Oral Selective FGFR3 Inhibitor for the Treatment of Urothelial Cancers and Achondroplasia.
J.Med.Chem., 67, 2024
9CD7
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FGFR3 Kinase Domain with Inhibitor TYRA-300
分子名称: (3P)-5-[(1R)-1-(3,5-dichloropyridin-4-yl)ethoxy]-3-{6-[6-(methanesulfonyl)-2,6-diazaspiro[3.3]heptan-2-yl]pyridin-3-yl}-1H-indazole, Fibroblast growth factor receptor 3, GLYCEROL, ...
著者Hoffman, I.H, Nelson, K.J, Rideout, M.C, Nix, J.C, Frye, C, Bensen, D.C, Hudkins, R.L.
登録日2024-06-24
公開日2024-09-25
最終更新日2024-10-02
実験手法X-RAY DIFFRACTION (2.53 Å)
主引用文献Discovery of TYRA-300: First Oral Selective FGFR3 Inhibitor for the Treatment of Urothelial Cancers and Achondroplasia.
J.Med.Chem., 67, 2024
9CE4
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Structure of CHK1 10-pt. mutant complex with LRRK2 indazole inhibitor compound 6
分子名称: (1S,4r)-4-[(1P)-5-chloro-1-(1-methyl-1H-pyrazol-4-yl)-1H-indazol-6-yl]-1-(oxetan-3-yl)piperidin-1-ium, 1,2-ETHANEDIOL, Serine/threonine-protein kinase Chk1
著者Palte, R.L, Zebisch, M, Henry, C, Barker, J.J.
登録日2024-06-26
公開日2024-09-18
最終更新日2024-10-02
実験手法X-RAY DIFFRACTION (1.31 Å)
主引用文献Discovery and Optimization of N-Heteroaryl Indazole LRRK2 Inhibitors.
J.Med.Chem., 67, 2024
9CER
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Guillardia theta Fanzor (GtFz) State 1
分子名称: Maltose/maltodextrin-binding periplasmic protein,Guillardia theta Fanzor1, RNA (142-MER), ZINC ION
著者Xu, P, Saito, M, Zhang, F.
登録日2024-06-27
公開日2024-09-11
最終更新日2024-10-02
実験手法ELECTRON MICROSCOPY (4.7 Å)
主引用文献Structural insights into the diversity and DNA cleavage mechanism of Fanzor.
Cell, 187, 2024
9CES
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Guillardia theta Fanzor (GtFz) State 2
分子名称: DNA (5'-D(P*AP*TP*GP*AP*CP*TP*TP*CP*TP*CP*TP*TP*AP*AP*AP*GP*GP*CP*CP*CP*CP*GP*GP*G)-3'), DNA (5'-D(P*CP*CP*CP*GP*GP*GP*GP*CP*CP*TP*TP*TP*AP*AP*G)-3'), Maltose/maltodextrin-binding periplasmic protein,Guillardia theta Fanzor1, ...
著者Xu, P, Saito, M, Zhang, F.
登録日2024-06-27
公開日2024-09-11
最終更新日2024-10-02
実験手法ELECTRON MICROSCOPY (3.28 Å)
主引用文献Structural insights into the diversity and DNA cleavage mechanism of Fanzor.
Cell, 187, 2024
9CET
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Guillardia theta Fanzor (GtFz) State 3
分子名称: DNA (28-MER), DNA (5'-D(P*AP*TP*GP*AP*CP*TP*TP*CP*TP*CP*TP*TP*AP*AP*AP*GP*GP*CP*CP*CP*CP*GP*GP*G)-3'), Maltose/maltodextrin-binding periplasmic protein,Guillardia theta Fanzor1, ...
著者Xu, P, Saito, M, Zhang, F.
登録日2024-06-27
公開日2024-09-11
最終更新日2024-10-02
実験手法ELECTRON MICROSCOPY (3 Å)
主引用文献Structural insights into the diversity and DNA cleavage mechanism of Fanzor.
Cell, 187, 2024
9CEU
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Spizellomyces punctatus Fanzor (SpuFz) State 1
分子名称: DNA (5'-D(P*CP*CP*TP*AP*TP*AP*GP*AP*TP*AP*TP*GP*CP*CP*CP*GP*GP*GP*TP*AP*CP*CP*G)-3'), DNA (5'-D(P*CP*GP*GP*TP*AP*CP*CP*CP*GP*GP*GP*CP*AP*TP*A)-3'), Maltose/maltodextrin-binding periplasmic protein,Spizellomyces punctatus Fanzor 1, ...
著者Xu, P, Saito, M, Zhang, F.
登録日2024-06-27
公開日2024-09-11
最終更新日2024-10-02
実験手法ELECTRON MICROSCOPY (3.29 Å)
主引用文献Structural insights into the diversity and DNA cleavage mechanism of Fanzor.
Cell, 187, 2024
9CEV
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Spizellomyces punctatus Fanzor (SpuFz) State 2
分子名称: DNA (35-MER), DNA (5'-D(P*CP*GP*GP*TP*AP*CP*CP*CP*GP*GP*GP*CP*AP*TP*A)-3'), MAGNESIUM ION, ...
著者Xu, P, Saito, M, Zhang, F.
登録日2024-06-27
公開日2024-09-11
最終更新日2024-10-02
実験手法ELECTRON MICROSCOPY (3.26 Å)
主引用文献Structural insights into the diversity and DNA cleavage mechanism of Fanzor.
Cell, 187, 2024
9CEW
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Spizellomyces punctatus Fanzor (SpuFz) State 3
分子名称: DNA (29-MER), DNA (5'-D(P*AP*AP*AP*AP*AP*AP*AP*AP*AP*AP*AP*AP*AP*AP*AP*AP*AP*AP*AP*AP*AP*AP*A)-3'), DNA (5'-D(P*CP*GP*GP*TP*AP*CP*CP*CP*GP*GP*GP*CP*AP*TP*A)-3'), ...
著者Xu, P, Saito, M, Zhang, F.
登録日2024-06-27
公開日2024-09-11
最終更新日2024-10-02
実験手法ELECTRON MICROSCOPY (2.88 Å)
主引用文献Structural insights into the diversity and DNA cleavage mechanism of Fanzor.
Cell, 187, 2024
9CEX
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Spizellomyces punctatus Fanzor (SpuFz) State 4
分子名称: DNA (29-MER), DNA (5'-D(*(MG)*(MG)P*AP*AP*AP*AP*AP*AP*AP*AP*AP*AP*AP*AP*AP*AP*AP*A)-3'), DNA (5'-D(P*CP*GP*GP*TP*AP*CP*CP*CP*GP*GP*GP*CP*AP*TP*A)-3'), ...
著者Xu, P, Saito, M, Zhang, F.
登録日2024-06-27
公開日2024-09-11
最終更新日2024-10-02
実験手法ELECTRON MICROSCOPY (3.27 Å)
主引用文献Structural insights into the diversity and DNA cleavage mechanism of Fanzor.
Cell, 187, 2024
9CEY
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Spizellomyces punctatus Fanzor (SpuFz) State 5
分子名称: DNA (26-MER), DNA (36-MER), MAGNESIUM ION, ...
著者Xu, P, Saito, M, Zhang, F.
登録日2024-06-27
公開日2024-09-11
最終更新日2024-10-02
実験手法ELECTRON MICROSCOPY (3.22 Å)
主引用文献Structural insights into the diversity and DNA cleavage mechanism of Fanzor.
Cell, 187, 2024
9CEZ
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Spizellomyces punctatus Fanzor (SpuFz) State 6
分子名称: DNA (27-MER), DNA (5'-D(P*TP*AP*CP*CP*CP*GP*GP*GP*CP*AP*TP*A)-3'), MAGNESIUM ION, ...
著者Xu, P, Saito, M, Zhang, F.
登録日2024-06-27
公開日2024-09-11
最終更新日2024-10-02
実験手法ELECTRON MICROSCOPY (3.41 Å)
主引用文献Structural insights into the diversity and DNA cleavage mechanism of Fanzor.
Cell, 187, 2024
9CF0
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Parasitella parasitica Fanzor (PpFz) State 1
分子名称: DNA non-target strand, DNA target strand, Maltose/maltodextrin-binding periplasmic protein,Parasitella parasitica Fanzor 1, ...
著者Xu, P, Saito, M, Zhang, F.
登録日2024-06-27
公開日2024-09-11
最終更新日2024-10-02
実験手法ELECTRON MICROSCOPY (3.47 Å)
主引用文献Structural insights into the diversity and DNA cleavage mechanism of Fanzor.
Cell, 187, 2024
9CF1
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Parasitella parasitica Fanzor (PpFz) State 2
分子名称: DNA non-target strand, DNA target strand, Maltose/maltodextrin-binding periplasmic protein,Parasitella parasitica Fanzor 1, ...
著者Xu, P, Saito, M, Zhang, F.
登録日2024-06-27
公開日2024-09-11
最終更新日2024-10-02
実験手法ELECTRON MICROSCOPY (3.52 Å)
主引用文献Structural insights into the diversity and DNA cleavage mechanism of Fanzor.
Cell, 187, 2024
9CF2
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Parasitella parasitica Fanzor (PpFz) State 3
分子名称: DNA non-target strand, DNA substrate model, DNA target strand, ...
著者Xu, P, Saito, M, Zhang, F.
登録日2024-06-27
公開日2024-09-11
最終更新日2024-10-02
実験手法ELECTRON MICROSCOPY (3.15 Å)
主引用文献Structural insights into the diversity and DNA cleavage mechanism of Fanzor.
Cell, 187, 2024
9CF3
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Parasitella parasitica Fanzor (PpFz) State 4
分子名称: DNA non-target strand, DNA target strand, MAGNESIUM ION, ...
著者Xu, P, Saito, M, Zhang, F.
登録日2024-06-27
公開日2024-09-11
最終更新日2024-10-02
実験手法ELECTRON MICROSCOPY (3.2 Å)
主引用文献Structural insights into the diversity and DNA cleavage mechanism of Fanzor.
Cell, 187, 2024
9CGX
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Alzheimer's Disease Seeded 0N3R Tau Fibrils
分子名称: Isoform Fetal-tau of Microtubule-associated protein tau
著者Duan, P, Dregni, A.J, Xu, H, Changolkar, L, Lee, V.M.-Y, Hong, M.
登録日2024-07-01
公開日2024-09-11
最終更新日2024-10-02
実験手法ELECTRON MICROSCOPY (2.97 Å)
主引用文献Alzheimer's disease seeded tau forms paired helical filaments yet lacks seeding potential.
J.Biol.Chem., 300, 2024
9CGZ
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Alzheimer's Disease Seeded Mixed 0N4R and 0N3R Tau Fibrils
分子名称: Isoform Fetal-tau of Microtubule-associated protein tau
著者Duan, P, Dregni, A.J, Xu, H, Changolkar, L, Lee, V.M.-Y, Hong, M.
登録日2024-07-01
公開日2024-09-11
最終更新日2024-10-02
実験手法ELECTRON MICROSCOPY (2.69 Å)
主引用文献Alzheimer's disease seeded tau forms paired helical filaments yet lacks seeding potential.
J.Biol.Chem., 300, 2024
9CSG
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Human Serum Albumin Bound to Cerastecin Compound 5e
分子名称: 2-(4-butylbenzene-1-sulfonamido)-5-(4-{3-carboxy-4-[4-(2-methoxyethyl)benzene-1-sulfonamido]anilino}-4-oxobutanamido)benzoic acid, Albumin, MYRISTIC ACID
著者Hruza, A, Klein, D.J, Ishchenko, A.
登録日2024-07-23
公開日2024-09-04
最終更新日2024-10-02
実験手法X-RAY DIFFRACTION (1.914 Å)
主引用文献Cerastecin Inhibition of the Lipooligosaccharide Transporter MsbA to Combat Acinetobacter baumannii : From Screening Impurity to In Vivo Efficacy.
J.Med.Chem., 67, 2024
9CSI
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A. baumannii MsbA Bound to Cerastecin Compound 5
分子名称: 3,3'-[(1,4-dioxobutane-1,4-diyl)bis(azanediyl)]bis[(4-butylbenzene-1-sulfonamido)benzoic acid], Lipid A export ATP-binding/permease protein MsbA, MAGNESIUM ION, ...
著者Klein, D.J, Ishchenko, A, Soisson, S, Cheng, R, Hennig, M.
登録日2024-07-23
公開日2024-09-04
最終更新日2024-10-02
実験手法X-RAY DIFFRACTION (2.8 Å)
主引用文献Cerastecin Inhibition of the Lipooligosaccharide Transporter MsbA to Combat Acinetobacter baumannii : From Screening Impurity to In Vivo Efficacy.
J.Med.Chem., 67, 2024

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件を2024-10-02に公開中

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