7PCN
 
 | BurG (holo) in complex with gonyenediol (14), trigonic acid (6) and DMS: Biosynthesis of cyclopropanol rings in bacterial toxins | 分子名称: | (2R)-2-oxidanyl-2-(1-oxidanylcyclopropyl)ethanoic acid, (METHYLSULFANYL)METHANE, 1,4-DIHYDRONICOTINAMIDE ADENINE DINUCLEOTIDE, ... | 著者 | Trottmann, F, Ishida, K, Ishida, M, Kries, H, Groll, M, Hertweck, C. | 登録日 | 2021-08-03 | 公開日 | 2022-08-10 | 最終更新日 | 2024-01-31 | 実験手法 | X-RAY DIFFRACTION (1.6 Å) | 主引用文献 | Pathogenic bacteria remodel central metabolic enzyme to build a cyclopropanol warhead. Nat.Chem., 14, 2022
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8ONC
 
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4XBC
 
 | 1.60 A resolution structure of Norovirus 3CL protease complex with a covalently bound dipeptidyl inhibitor (1R,2S)-2-({N-[(benzyloxy)carbonyl]-3-cyclohexyl-L-alanyl}amino)-1-hydroxy-3-[(3S)-2-oxopyrrolidin-3-yl]propane-1-sulfonic acid (Hexagonal Form) | 分子名称: | (1R,2S)-2-({N-[(benzyloxy)carbonyl]-3-cyclohexyl-L-alanyl}amino)-1-hydroxy-3-[(3S)-2-oxopyrrolidin-3-yl]propane-1-sulfonic acid, 3C-LIKE PROTEASE, TETRAETHYLENE GLYCOL | 著者 | Lovell, S, Battaile, K.P, Mehzabeen, N, Kankanamalage, A.C.G, Kim, Y, Weerawarna, P.M, Uy, R.A.Z, Damalanka, V.C, Mandadapu, S.R, Alliston, K.R, Groutas, W.C, Chang, K.-O. | 登録日 | 2014-12-16 | 公開日 | 2015-03-25 | 最終更新日 | 2024-10-23 | 実験手法 | X-RAY DIFFRACTION (1.6 Å) | 主引用文献 | Structure-Guided Design and Optimization of Dipeptidyl Inhibitors of Norovirus 3CL Protease. Structure-Activity Relationships and Biochemical, X-ray Crystallographic, Cell-Based, and In Vivo Studies. J.Med.Chem., 58, 2015
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6OBP
 
 | Reconstituted PP1 holoenzyme | 分子名称: | CHLORIDE ION, MANGANESE (II) ION, PHOSPHATE ION, ... | 著者 | Choy, M.S, Moon, T.M, Bray, J.A, Archuleta, T.L, Shi, W, Peti, W, Page, R. | 登録日 | 2019-03-21 | 公開日 | 2019-09-18 | 最終更新日 | 2023-10-11 | 実験手法 | X-RAY DIFFRACTION (2.7 Å) | 主引用文献 | SDS22 selectively recognizes and traps metal-deficient inactive PP1. Proc.Natl.Acad.Sci.USA, 116, 2019
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5E99
 
 | Bovine Fab fragment F08_B11 | 分子名称: | Fab F08_B11 heavy chain, Fab F08_B11 light chain | 著者 | Stanfield, R.L, Wilson, I.A. | 登録日 | 2015-10-14 | 公開日 | 2016-08-24 | 最終更新日 | 2024-10-16 | 実験手法 | X-RAY DIFFRACTION (2.06 Å) | 主引用文献 | Conservation and diversity in the ultralong third heavy-chain complementarity-determining region of bovine antibodies. Sci Immunol, 1, 2016
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8W4S
 
 | Crystal structure of PDE5A in complex with CVT-313 | 分子名称: | 2,2'-{[6-{[(4-methoxyphenyl)methyl]amino}-9-(propan-2-yl)-9H-purin-2-yl]azanediyl}di(ethan-1-ol), MAGNESIUM ION, ZINC ION, ... | 著者 | Liu, J.Y, Li, M.J, Xu, Y.C. | 登録日 | 2023-08-24 | 公開日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (1.848 Å) | 主引用文献 | Drug repurposing and structure-based discovery of new PDE4 and PDE5 inhibitors. Eur.J.Med.Chem., 262, 2023
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5XJ6
 
 | Crystal structure of PlsY (YgiH), an integral membrane glycerol 3-phosphate acyltransferase - the glycerol 3-phosphate form | 分子名称: | (2R)-2,3-dihydroxypropyl (9Z)-octadec-9-enoate, Glycerol-3-phosphate acyltransferase, PHOSPHATE ION, ... | 著者 | Li, Z, Tang, Y, Li, D. | 登録日 | 2017-04-30 | 公開日 | 2017-12-06 | 最終更新日 | 2024-11-06 | 実験手法 | X-RAY DIFFRACTION (2.37 Å) | 主引用文献 | Structural insights into the committed step of bacterial phospholipid biosynthesis. Nat Commun, 8, 2017
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8VCW
 
 | X-Ray Crystal Structure of the biotin synthase from B. obeum | 分子名称: | 2-[BIS-(2-HYDROXY-ETHYL)-AMINO]-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, 6-(5-METHYL-2-OXO-IMIDAZOLIDIN-4-YL)-HEXANOIC ACID, Biotin synthase, ... | 著者 | Lachowicz, J.C, Grove, T.L. | 登録日 | 2023-12-14 | 公開日 | 2024-01-24 | 最終更新日 | 2024-02-07 | 実験手法 | X-RAY DIFFRACTION (1.35 Å) | 主引用文献 | Discovery of a Biotin Synthase That Utilizes an Auxiliary 4Fe-5S Cluster for Sulfur Insertion. J.Am.Chem.Soc., 146, 2024
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8U9F
 
 | Crystal structure of Bacteroides thetaiotamicron BT1285 in complex with NaI | 分子名称: | 1,2-ETHANEDIOL, Endo-beta-N-acetylglucosaminidase, IODIDE ION, ... | 著者 | Sastre, D.E, Navarro, M.V.A.S, Sundberg, E.J. | 登録日 | 2023-09-19 | 公開日 | 2024-05-29 | 最終更新日 | 2024-12-25 | 実験手法 | X-RAY DIFFRACTION (1.08 Å) | 主引用文献 | Human gut microbes express functionally distinct endoglycosidases to metabolize the same N-glycan substrate. Nat Commun, 15, 2024
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6R3P
 
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8UAS
 
 | Rhodococcus ruber Alcohol Dehydrogenase NADH Biomimetic Complex - Compound 1a | 分子名称: | 1-[3-[~{tert}-butyl(dimethyl)silyl]oxypropyl]pyridine-3-carboxamide, CITRIC ACID, ISOPROPYL ALCOHOL, ... | 著者 | Wilson, L.A, Guddat, L.W, Schenk, G, Scott, C. | 登録日 | 2023-09-22 | 公開日 | 2024-07-03 | 実験手法 | X-RAY DIFFRACTION (2.2 Å) | 主引用文献 | Structural Characterization of Enzymatic Interactions with Functional Nicotinamide Cofactor Biomimetics Catalysts, 14, 2024
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4XDZ
 
 | Holo structure of ketol-acid reductoisomerase from Ignisphaera aggregans | 分子名称: | 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID, GLYCEROL, Ketol-acid reductoisomerase, ... | 著者 | Cahn, J.K.B, Brinkmann-Chen, S, Arnold, F.H. | 登録日 | 2014-12-20 | 公開日 | 2015-04-22 | 最終更新日 | 2023-09-27 | 実験手法 | X-RAY DIFFRACTION (1.15 Å) | 主引用文献 | Cofactor specificity motifs and the induced fit mechanism in class I ketol-acid reductoisomerases. Biochem.J., 468, 2015
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8TV3
 
 | Fab 221-5 in complex with OspA | 分子名称: | 1,2-ETHANEDIOL, CHLORIDE ION, Heavy chain of human monoclonal Fab 221-5, ... | 著者 | Rudolph, M.J, Mantis, N. | 登録日 | 2023-08-17 | 公開日 | 2024-08-28 | 最終更新日 | 2024-10-09 | 実験手法 | X-RAY DIFFRACTION (2.312 Å) | 主引用文献 | Fab 221-5 in complex with OspA To Be Published
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6OBC
 
 | Ricin A chain bound to camelid | 分子名称: | 1,2-ETHANEDIOL, CHLORIDE ION, Ricin A chain, ... | 著者 | Rudolph, M.J. | 登録日 | 2019-03-20 | 公開日 | 2020-04-01 | 最終更新日 | 2024-10-30 | 実験手法 | X-RAY DIFFRACTION (1.762 Å) | 主引用文献 | Intracellular Neutralization of Ricin Toxin by Single-domain Antibodies Targeting the Active Site. J.Mol.Biol., 432, 2020
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8IT9
 
 | Co-crystal structure of FTO bound to 22 | 分子名称: | 2-OXOGLUTARIC ACID, 2-[(2,6-diethyl-4-pyridin-4-yl-phenyl)amino]-6-(1,4-oxazepan-4-ylmethyl)benzoic acid, Alpha-ketoglutarate-dependent dioxygenase FTO | 著者 | Yang, C.-G, Gan, J.H. | 登録日 | 2023-03-22 | 公開日 | 2024-02-14 | 実験手法 | X-RAY DIFFRACTION (2.14 Å) | 主引用文献 | Rational Design of RNA Demethylase FTO Inhibitors with Enhanced Antileukemia Drug-Like Properties. J.Med.Chem., 66, 2023
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9MS4
 
 | Crystal structure of an expansin (Xa_EXLX1) from Xanthomonas sacchari | 分子名称: | 1,2-ETHANEDIOL, 2-hydroxy-3,5-dinitrobenzoic acid, Expansin (Peptidoglycan-binding protein) | 著者 | Smith, C.A, Buchko, G.W, Momeni, M.H, Master, E.R. | 登録日 | 2025-01-09 | 公開日 | 2025-05-21 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Insights into the action of phylogenetically diverse microbial expansins To Be Published
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8G9V
 
 | Crystal structures of 17-beta-hydroxysteroid dehydrogenase 13 | 分子名称: | 17-beta-hydroxysteroid dehydrogenase 13, 4-{[2,5-dimethyl-3-(4-methylbenzene-1-sulfonyl)benzene-1-sulfonyl]amino}benzoic acid, NICOTINAMIDE-ADENINE-DINUCLEOTIDE, ... | 著者 | Liu, S. | 登録日 | 2023-02-22 | 公開日 | 2023-08-09 | 最終更新日 | 2023-09-06 | 実験手法 | X-RAY DIFFRACTION (2.645 Å) | 主引用文献 | Structural basis of lipid-droplet localization of 17-beta-hydroxysteroid dehydrogenase 13. Nat Commun, 14, 2023
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7QE9
 
 | Human cationic trypsin (TRY1) complexed with serine protease inhibitor Kazal type 1 N34S (SPINK1 N34S) | 分子名称: | SULFATE ION, Serine protease inhibitor Kazal-type 1, Trypsin-1 | 著者 | Nagel, F, Palm, G.J, Delcea, M, Lammers, M. | 登録日 | 2021-12-01 | 公開日 | 2022-03-30 | 最終更新日 | 2024-10-16 | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | 主引用文献 | Structural and Biophysical Insights into SPINK1 Bound to Human Cationic Trypsin. Int J Mol Sci, 23, 2022
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8P19
 
 | USP28 USP domain apo | 分子名称: | 1,2-ETHANEDIOL, CHLORIDE ION, Ubiquitin carboxyl-terminal hydrolase 28 | 著者 | Sauer, F, Karal Nair, R, Kisker, C. | 登録日 | 2023-05-11 | 公開日 | 2024-05-22 | 最終更新日 | 2024-12-04 | 実験手法 | X-RAY DIFFRACTION (2.45 Å) | 主引用文献 | Structural basis for the bi-specificity of USP25 and USP28 inhibitors. Embo Rep., 25, 2024
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8CJC
 
 | F515A variant of the CODH/ACS complex of C. hydrogenoformans | 分子名称: | (4S)-2-METHYL-2,4-PENTANEDIOL, ACETATE ION, CO-methylating acetyl-CoA synthase, ... | 著者 | Ruickoldt, J, Jeoung, J, Lennartz, F, Dobbek, H. | 登録日 | 2023-02-13 | 公開日 | 2024-02-21 | 最終更新日 | 2024-07-31 | 実験手法 | X-RAY DIFFRACTION (2.22 Å) | 主引用文献 | Coupling CO 2 Reduction and Acetyl-CoA Formation: The Role of a CO Capturing Tunnel in Enzymatic Catalysis. Angew.Chem.Int.Ed.Engl., 63, 2024
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5NQP
 
 | Structure of a fHbp(V1.4):PorA(P1.16) chimera. Fusion at fHbp position 151. | 分子名称: | 1,2-ETHANEDIOL, CHLORIDE ION, Factor H binding protein variant B16_001,Major outer membrane protein P.IA,Factor H binding protein variant B16_001, ... | 著者 | Johnson, S, Hollingshead, S, Lea, S.M, Tang, C.M. | 登録日 | 2017-04-20 | 公開日 | 2018-02-28 | 最終更新日 | 2025-10-01 | 実験手法 | X-RAY DIFFRACTION (2.86 Å) | 主引用文献 | Structure-based design of chimeric antigens for multivalent protein vaccines. Nat Commun, 9, 2018
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7RM2
 
 | Room temperature X-ray structure of SARS-CoV-2 main protease (Mpro) in complex with Mcule-CSR-494190-S1 | 分子名称: | 3C-like proteinase, 6-[4-(3,5-dichloro-4-methylphenyl)piperazine-1-carbonyl]pyrimidine-2,4(1H,3H)-dione | 著者 | Kovalevsky, A, Kneller, D.W, Coates, L. | 登録日 | 2021-07-26 | 公開日 | 2021-11-10 | 最終更新日 | 2023-10-18 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Structural, Electronic, and Electrostatic Determinants for Inhibitor Binding to Subsites S1 and S2 in SARS-CoV-2 Main Protease. J.Med.Chem., 64, 2021
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7RME
 
 | Room temperature X-ray structure of SARS-CoV-2 main protease (Mpro) in complex with HL-3-52 | 分子名称: | 3C-like proteinase, 6-{4-[4-chloro-3-(trifluoromethyl)phenyl]piperazine-1-carbonyl}pyrimidine-2,4(1H,3H)-dione | 著者 | Kovalevsky, A, Kneller, D.W, Coates, L. | 登録日 | 2021-07-27 | 公開日 | 2021-11-10 | 最終更新日 | 2023-10-18 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Structural, Electronic, and Electrostatic Determinants for Inhibitor Binding to Subsites S1 and S2 in SARS-CoV-2 Main Protease. J.Med.Chem., 64, 2021
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7AL6
 
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4XRZ
 
 | Human Cytochrome P450 2D6 BACE1 Inhibitor 6 Complex | 分子名称: | (4aR,6R,8aS)-8a-(2,4-difluorophenyl)-6-(1H-pyrazol-4-yl)-4,4a,5,6,8,8a-hexahydropyrano[3,4-d][1,3]thiazin-2-amine, Cytochrome P450 2D6, GLYCEROL, ... | 著者 | Johnson, E.F, Fan, Y. | 登録日 | 2015-01-21 | 公開日 | 2015-05-20 | 最終更新日 | 2023-09-27 | 実験手法 | X-RAY DIFFRACTION (2.4 Å) | 主引用文献 | Utilizing Structures of CYP2D6 and BACE1 Complexes To Reduce Risk of Drug-Drug Interactions with a Novel Series of Centrally Efficacious BACE1 Inhibitors. J.Med.Chem., 58, 2015
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