4W1W
 
 | Crystal structure of 7,8-diaminopelargonic acid synthase (BioA) from Mycobacterium tuberculosis, complexed with 7-(diethylamino)-3-(thiophene-2-carbonyl)-2H-chromen-2-one | Descriptor: | 1,2-ETHANEDIOL, 7-(diethylamino)-3-(thiophen-2-ylcarbonyl)-2H-chromen-2-one, Adenosylmethionine-8-amino-7-oxononanoate aminotransferase, ... | Authors: | Finzel, B.C, Ran, D. | Deposit date: | 2014-08-13 | Release date: | 2015-02-04 | Last modified: | 2023-12-27 | Method: | X-RAY DIFFRACTION (1.9 Å) | Cite: | Target-Based Identification of Whole-Cell Active Inhibitors of Biotin Biosynthesis in Mycobacterium tuberculosis. Chem.Biol., 22, 2015
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8RMZ
 
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8AK5
 
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8AKB
 
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8AKE
 
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5IYG
 
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5IYJ
 
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1D48
 
 | STRUCTURE OF THE PURE-SPERMINE FORM OF Z-DNA (MAGNESIUM FREE) AT 1 ANGSTROM RESOLUTION | Descriptor: | DNA (5'-D(*CP*GP*CP*GP*CP*G)-3'), SPERMINE | Authors: | Egli, M, Williams, L.D, Gao, Q, Rich, A. | Deposit date: | 1991-09-11 | Release date: | 1992-04-15 | Last modified: | 2024-02-07 | Method: | X-RAY DIFFRACTION (1 Å) | Cite: | Structure of the pure-spermine form of Z-DNA (magnesium free) at 1-A resolution. Biochemistry, 30, 1991
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1D64
 
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9MGY
 
 | Cryo-EM structure of Human NLRP3 complex with compound 1 | Descriptor: | (2M)-2-(6-{[(3R)-1-methylpiperidin-3-yl]amino}pyridazin-3-yl)-5-(trifluoromethyl)phenol, ADENOSINE-5'-TRIPHOSPHATE, NACHT, ... | Authors: | Mammoliti, O, Carbajo, R.J, Perez-Benito, L, Yu, X, Prieri, M.L.C, Bontempi, L, Embrechts, S, Paesmans, I, Bassi, M, Bhattacharya, A, Roman, S.C, Hoog, S.D, Demin, S, Gijsen, H.J.M, Hache, G, Jacobs, T, Jerhaoui, S, Leenaerts, J, Lutter, F.H, Matico, R, Oehlrich, D, Perrier, M, Ryabchuk, P, Schepens, W, Sharma, S, Somers, M, Suarez, J, Surkyn, M, Opdenbosch, N.V, Verhulst, T, Bottelbergs, A. | Deposit date: | 2024-12-11 | Release date: | 2025-02-26 | Last modified: | 2025-03-12 | Method: | ELECTRON MICROSCOPY (2.9 Å) | Cite: | Discovery of Potent and Brain-Penetrant Bicyclic NLRP3 Inhibitors with Peripheral and Central In Vivo Activity. J.Med.Chem., 68, 2025
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8HVQ
 
 | Crystal structure of haloacid dehalogenase-like hydrolase family enzyme from Staphylococcus lugdunensis | Descriptor: | 1,2-ETHANEDIOL, Cof-type HAD-IIB family hydrolase, DI(HYDROXYETHYL)ETHER, ... | Authors: | Kaur, H, Mahto, J.K, Kumar, P, Sharma, A.K. | Deposit date: | 2022-12-27 | Release date: | 2023-12-27 | Last modified: | 2024-05-29 | Method: | X-RAY DIFFRACTION (1.73 Å) | Cite: | Characterization of haloacid dehalogenase superfamily acid phosphatase from Staphylococcus lugdunensis. Arch.Biochem.Biophys., 753, 2024
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9QYZ
 
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7QXC
 
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9MQ5
 
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9MS1
 
 | Crystal structure of human CYP3A4 in complex with SJYHJ-111 | Descriptor: | Cytochrome P450 3A4, N'-(2-chlorophenyl)-N-[(3-hydroxyphenyl)methyl]-N-[(2P)-2-(1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl]urea, PROTOPORPHYRIN IX CONTAINING FE | Authors: | Jingheng, W, Nithianantham, S, Miller, D.J, Chen, T. | Deposit date: | 2025-01-09 | Release date: | 2025-04-16 | Last modified: | 2025-04-23 | Method: | X-RAY DIFFRACTION (3.4 Å) | Cite: | Decoding the selective chemical modulation of CYP3A4. Nat Commun, 16, 2025
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9MGN
 
 | Crystal structure of PRMT5:MEP50 in complex with MTA and compound 41 | Descriptor: | 1,2-ETHANEDIOL, 2-(cyclobutylamino)-N-[(2S)-2-hydroxy-3-{6-[(1H-pyrazol-4-yl)methoxy]-3,4-dihydroisoquinolin-2(1H)-yl}propyl]pyridine-4-carboxamide, 5'-DEOXY-5'-METHYLTHIOADENOSINE, ... | Authors: | Whittington, D.A. | Deposit date: | 2024-12-11 | Release date: | 2025-03-05 | Method: | X-RAY DIFFRACTION (2.82 Å) | Cite: | MTA-Cooperative PRMT5 Inhibitors: Mechanism Switching Through Structure-Based Design. J.Med.Chem., 68, 2025
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4R2P
 
 | Wilms Tumor Protein (WT1) zinc fingers in complex with hydroxymethylated DNA | Descriptor: | 1,2-ETHANEDIOL, DNA (5'-D(*AP*GP*CP*GP*TP*GP*GP*GP*(5HC)P*GP*T)-3'), DNA (5'-D(*TP*AP*(5HC)P*GP*CP*CP*CP*AP*CP*GP*C)-3'), ... | Authors: | Hashimoto, H, Olanrewaju, Y.O, Zheng, Y, Wilson, G.G, Zhang, X, Cheng, X. | Deposit date: | 2014-08-12 | Release date: | 2014-10-08 | Last modified: | 2023-09-20 | Method: | X-RAY DIFFRACTION (1.788 Å) | Cite: | Wilms tumor protein recognizes 5-carboxylcytosine within a specific DNA sequence. Genes Dev., 28, 2014
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9S48
 
 | Human SIRT2 in Complex with RW-80 | Descriptor: | 1,2-ETHANEDIOL, ACETATE ION, NAD-dependent protein deacetylase sirtuin-2, ... | Authors: | Wirawan, R, Frei, M, Heider, A, Papenkordt, N, Friedrich, F, Wein, T, Jung, M, Groll, M, Huber, E.M, Bracher, F. | Deposit date: | 2025-07-25 | Release date: | 2025-08-20 | Last modified: | 2025-09-24 | Method: | X-RAY DIFFRACTION (1.45 Å) | Cite: | Tailored SirReal-type inhibitors enhance SIRT2 inhibition through ligand stabilization and disruption of NAD + co-factor binding. Rsc Med Chem, 2025
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9MZZ
 
 | Crystal structure of RIPK1 with compound 36 | Descriptor: | (2S,5S)-4-(3,3-difluoro-2,2-dimethylpropanoyl)-2,3,4,5-tetrahydro-2,5-methanopyrido[3,4-f][1,4]oxazepine-9-carbonitrile, IODIDE ION, Receptor-interacting serine/threonine-protein kinase 1 | Authors: | Lesburg, C.A, Palte, R.L, Maskos, K, Thomsen, M, Lammens, A. | Deposit date: | 2025-01-23 | Release date: | 2025-05-28 | Method: | X-RAY DIFFRACTION (2.68 Å) | Cite: | The Discovery of Bridged Benzoazepine Amides as Selective Allosteric Modulators of RIPK1. Acs Med.Chem.Lett., 16, 2025
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9UUU
 
 | Cryo-EM structure of Na+-translocating NADH-ubiquinone oxidoreductase from Vibrio cholerae reduced by NADH | Descriptor: | 1,4-DIHYDRONICOTINAMIDE ADENINE DINUCLEOTIDE, CALCIUM ION, FE2/S2 (INORGANIC) CLUSTER, ... | Authors: | Ishikawa-Fukuda, M, Kishikawa, J, Kato, T, Murai, M. | Deposit date: | 2025-05-08 | Release date: | 2025-06-25 | Method: | ELECTRON MICROSCOPY (3.17 Å) | Cite: | The Na + -pumping mechanism driven by redox reactions in the NADH-quinone oxidoreductase from Vibrio cholerae relies on dynamic conformational changes. Biorxiv, 2025
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9MGQ
 
 | Crystal structure of PRMT5:MEP50 in complex with sinefungin and compound 47 | Descriptor: | 1,2-ETHANEDIOL, 2-(cyclobutylamino)-N-{(2R)-2-hydroxy-2-[(3S)-1,2,3,4-tetrahydroisoquinolin-3-yl]ethyl}pyridine-4-carboxamide, DI(HYDROXYETHYL)ETHER, ... | Authors: | Whittington, D.A. | Deposit date: | 2024-12-11 | Release date: | 2025-03-05 | Method: | X-RAY DIFFRACTION (1.85 Å) | Cite: | MTA-Cooperative PRMT5 Inhibitors: Mechanism Switching Through Structure-Based Design. J.Med.Chem., 68, 2025
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4RDS
 
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9M5S
 
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8ERH
 
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9NXI
 
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