| 4MXV 
   
  | | Structure of Lymphotoxin alpha bound to anti-LTa Fab |  | Descriptor: | Lymphotoxin-alpha, anti-Lymphotoxin alpha antibody heavy chain, anti-Lymphotoxin alpha antibody light chain |  | Authors: | Yin, J.P,  Hymowitz, S.G. |  | Deposit date: | 2013-09-26 |  | Release date: | 2013-11-13 |  | Last modified: | 2024-10-09 |  | Method: | X-RAY DIFFRACTION (3.2 Å) |  | Cite: | Dimerization of LT beta R by LT alpha 1 beta 2 is necessary and sufficient for signal transduction. Proc.Natl.Acad.Sci.USA, 110, 2013
 
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| 7RWN 
   
  | | Crystal Structure of BPTF bromodomain in complex with 4-chloro-5-{4-[(dimethylamino)methyl]anilino}-2-methylpyridazin-3(2H)-one |  | Descriptor: | 1,2-ETHANEDIOL, 4-chloro-5-{4-[(dimethylamino)methyl]anilino}-2-methylpyridazin-3(2H)-one, Nucleosome-remodeling factor subunit BPTF |  | Authors: | Zahid, H,  Buchholz, C,  Johnson, J.A,  Shi, K,  Aihara, H,  Pomerantz, W.C.K. |  | Deposit date: | 2021-08-20 |  | Release date: | 2022-08-24 |  | Last modified: | 2023-10-18 |  | Method: | X-RAY DIFFRACTION (1.39 Å) |  | Cite: | New Design Rules for Developing Potent Cell-Active Inhibitors of the Nucleosome Remodeling Factor (NURF) via BPTF Bromodomain Inhibition. J.Med.Chem., 64, 2021
 
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| 3V50 
   
  | | Complex of SHV S130G mutant beta-lactamase complexed to SA2-13 |  | Descriptor: | (3R)-4-[(4-CARBOXYBUTANOYL)OXY]-N-[(1E)-3-OXOPROP-1-EN-1-YL]-3-SULFINO-D-VALINE, Beta-lactamase, CYCLOHEXYL-HEXYL-BETA-D-MALTOSIDE |  | Authors: | Wei, K,  van den Akker, F. |  | Deposit date: | 2011-12-15 |  | Release date: | 2012-08-08 |  | Last modified: | 2024-11-27 |  | Method: | X-RAY DIFFRACTION (1.45 Å) |  | Cite: | The importance of the trans-enamine intermediate as a beta-lactamase inhibition strategy  probed in inhibitor-resistant SHV beta-lactamase variants. Chemmedchem, 7, 2012
 
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| 7Y11 
   
  | | Crystal structure of AtSFH5-Sec14 in complex with egg PA |  | Descriptor: | (2R)-1-(hexadecanoyloxy)-3-(phosphonooxy)propan-2-yl (9Z)-octadec-9-enoate, CHLORIDE ION, NICKEL (II) ION, ... |  | Authors: | Lu, Y.Q,  Wang, X.Q,  Luo, Z.P,  Wu, J.W. |  | Deposit date: | 2022-06-06 |  | Release date: | 2023-04-19 |  | Last modified: | 2023-11-29 |  | Method: | X-RAY DIFFRACTION (1.95 Å) |  | Cite: | Arabidopsis Sec14 proteins (SFH5 and SFH7) mediate interorganelle transport of phosphatidic acid and regulate chloroplast development. Proc.Natl.Acad.Sci.USA, 120, 2023
 
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| 7RXU 
   
  | | Crystal structure of Cj1090c |  | Descriptor: | 1,2-ETHANEDIOL, GLYCEROL, Lipoprotein |  | Authors: | Kim, Y,  Yeo, H.J. |  | Deposit date: | 2021-08-23 |  | Release date: | 2022-08-31 |  | Last modified: | 2024-05-22 |  | Method: | X-RAY DIFFRACTION (2.4 Å) |  | Cite: | Crystal structure of Campylobacter jejuni lipoprotein Cj1090c. Proteins, 91, 2023
 
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| 1ZL7 
   
  | | Crystal structure of catalytically-active phospholipase A2 with bound calcium |  | Descriptor: | CALCIUM ION, GLYCEROL, hypotensive phospholipase A2 |  | Authors: | Murakami, M.T,  Cintra, A.C,  Gabdoulkhakov, A,  Genov, N,  Betzel, C,  Arni, R.K. |  | Deposit date: | 2005-05-05 |  | Release date: | 2006-04-25 |  | Last modified: | 2024-10-16 |  | Method: | X-RAY DIFFRACTION (1.6 Å) |  | Cite: | Insights into metal ion binding in phospholipases A(2): ultra high-resolution crystal structures of an acidic phospholipase A(2) in the Ca(2+) free and bound states. Biochimie, 88, 2006
 
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| 5F0L 
   
  | | Structure of retromer VPS26-VPS35 subunits bound to SNX3 and DMT1 |  | Descriptor: | 1,2-ETHANEDIOL, GLYCEROL, Natural resistance-associated macrophage protein 2, ... |  | Authors: | Lucas, M,  Gershlick, D,  Vidaurrazaga, A,  Rojas, A.L,  Bonifacino, J.S,  Hierro, A. |  | Deposit date: | 2015-11-27 |  | Release date: | 2016-12-07 |  | Last modified: | 2024-01-10 |  | Method: | X-RAY DIFFRACTION (3.2 Å) |  | Cite: | Structural Mechanism for Cargo Recognition by the Retromer Complex. Cell, 167, 2016
 
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| 4N4E 
   
  | | Thermolysin in complex with UBTLN58 |  | Descriptor: | CALCIUM ION, DIMETHYL SULFOXIDE, GLYCEROL, ... |  | Authors: | Krimmer, S.G,  Heine, A,  Klebe, G. |  | Deposit date: | 2013-10-08 |  | Release date: | 2014-04-02 |  | Last modified: | 2023-09-20 |  | Method: | X-RAY DIFFRACTION (1.13 Å) |  | Cite: | Methyl, Ethyl, Propyl, Butyl: Futile But Not for Water, as the Correlation of Structure and Thermodynamic Signature Shows in a Congeneric Series of Thermolysin Inhibitors. Chemmedchem, 4, 2014
 
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| 2OLE 
   
  | | Crystal Structure Of Human Dipeptidyl Peptidase IV (DPPIV) Complex With Cyclic Hydrazine Derivatives |  | Descriptor: | (2R)-4-(2-BENZOYL-1,2-DIAZEPAN-1-YL)-4-OXO-1-(2,4,5-TRIFLUOROPHENYL)BUTAN-2-AMINE, Dipeptidyl peptidase 4 |  | Authors: | Kim, S.S,  Ahn, J.H,  Lee, J.O. |  | Deposit date: | 2007-01-19 |  | Release date: | 2008-01-22 |  | Last modified: | 2024-11-06 |  | Method: | X-RAY DIFFRACTION (2.4 Å) |  | Cite: | Synthesis, biological evaluation and structural determination of beta-aminoacyl-containing cyclic hydrazine derivatives as dipeptidyl peptidase IV (DPP-IV) inhibitors Bioorg.Med.Chem.Lett., 17, 2007
 
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| 1YVF 
   
  | | Hepatitis C virus NS5B RNA-dependent RNA polymerase complex with inhibitor PHA-00729145 |  | Descriptor: | (2Z)-2-(BENZOYLAMINO)-3-[4-(2-BROMOPHENOXY)PHENYL]-2-PROPENOIC ACID, CHLORIDE ION, GLYCEROL, ... |  | Authors: | Pfefferkorn, J.A,  Greene, M.L,  Nugent, R.A,  Gross, R.J,  Mitchell, M.A,  Finzel, B.C,  Harris, M.S,  Wells, P.A,  Shelly, J.A,  Anstadt, R.A,  Kilkuskie, R.E,  Kopta, L.A,  Schwende, F.J. |  | Deposit date: | 2005-02-15 |  | Release date: | 2005-04-19 |  | Last modified: | 2024-02-14 |  | Method: | X-RAY DIFFRACTION (2.5 Å) |  | Cite: | Inhibitors of HCV NS5B polymerase. Part 1: Evaluation of the southern region of (2Z)-2-(benzoylamino)-3-(5-phenyl-2-furyl)acrylic acid. Bioorg.Med.Chem.Lett., 15, 2005
 
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| 9FXU 
   
  | | Crystal Structure of Autotaxin (ENPP2) with Type VI Inhibitor, a Novel Class of Inhibitors with Three-Point Lock Binding Mode |  | Descriptor: | CALCIUM ION, GLYCEROL, IODIDE ION, ... |  | Authors: | Borza, R,  Joosten, R.P,  Perrakis, A. |  | Deposit date: | 2024-07-02 |  | Release date: | 2025-04-23 |  | Last modified: | 2025-04-30 |  | Method: | X-RAY DIFFRACTION (2.25 Å) |  | Cite: | Design, Synthesis, and Biological Implications of Autotaxin inhibitors with a Three-Point lock binding mode. Bioorg.Med.Chem., 124, 2025
 
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| 4MTW 
   
  | | Thermolysin in complex with UBTLN36 |  | Descriptor: | CALCIUM ION, DIMETHYL SULFOXIDE, GLYCEROL, ... |  | Authors: | Krimmer, S.G,  Heine, A,  Klebe, G. |  | Deposit date: | 2013-09-20 |  | Release date: | 2014-04-02 |  | Last modified: | 2023-09-20 |  | Method: | X-RAY DIFFRACTION (1.32 Å) |  | Cite: | Methyl, Ethyl, Propyl, Butyl: Futile But Not for Water, as the Correlation of Structure and Thermodynamic Signature Shows in a Congeneric Series of Thermolysin Inhibitors. Chemmedchem, 4, 2014
 
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| 4MUD 
   
  |  | 
| 9FXY 
   
  | | Crystal Structure of Autotaxin (ENPP2) with Type IV Inhibitor |  | Descriptor: | 3-(3-((4-(4-fluorophenyl)thiazol-2-yl)(methyl)amino)-6-(1-(methylsulfonyl)piperidin-4-yl)imidazo[1,2-b]pyridazin-2-yl)propanenitrile, CALCIUM ION, GLYCEROL, ... |  | Authors: | Borza, R,  Joosten, R.P,  Perrakis, A. |  | Deposit date: | 2024-07-02 |  | Release date: | 2025-04-23 |  | Last modified: | 2025-04-30 |  | Method: | X-RAY DIFFRACTION (2 Å) |  | Cite: | Design, Synthesis, and Biological Implications of Autotaxin inhibitors with a Three-Point lock binding mode. Bioorg.Med.Chem., 124, 2025
 
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| 3UUE 
   
  | | Crystal structure of mono- and diacylglycerol lipase from Malassezia globosa |  | Descriptor: | CHLORIDE ION, GLYCEROL, LIP1, ... |  | Authors: | Xu, T,  Xu, J,  Hou, S,  Liu, J. |  | Deposit date: | 2011-11-28 |  | Release date: | 2012-04-25 |  | Last modified: | 2024-11-13 |  | Method: | X-RAY DIFFRACTION (1.45 Å) |  | Cite: | Crystal structure of a mono- and diacylglycerol lipase from Malassezia globosa reveals a novel lid conformation and insights into the substrate specificity. J.Struct.Biol., 178, 2012
 
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| 4MWP 
   
  | | Thermolysin in complex with UBTLN46 |  | Descriptor: | CALCIUM ION, DIMETHYL SULFOXIDE, GLYCEROL, ... |  | Authors: | Krimmer, S.G,  Heine, A,  Klebe, G. |  | Deposit date: | 2013-09-25 |  | Release date: | 2014-04-02 |  | Last modified: | 2023-09-20 |  | Method: | X-RAY DIFFRACTION (1.23 Å) |  | Cite: | Methyl, Ethyl, Propyl, Butyl: Futile But Not for Water, as the Correlation of Structure and Thermodynamic Signature Shows in a Congeneric Series of Thermolysin Inhibitors. Chemmedchem, 4, 2014
 
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| 2P8S 
   
  | | Human dipeptidyl peptidase IV/CD26 in complex with a cyclohexalamine inhibitor |  | Descriptor: | (1S,2R,5S)-5-[3-(TRIFLUOROMETHYL)-5,6-DIHYDRO[1,2,4]TRIAZOLO[4,3-A]PYRAZIN-7(8H)-YL]-2-(2,4,5-TRIFLUOROPHENYL)CYCLOHEXANAMINE, 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... |  | Authors: | Scapin, G,  Biftu, T. |  | Deposit date: | 2007-03-23 |  | Release date: | 2007-05-22 |  | Last modified: | 2024-10-16 |  | Method: | X-RAY DIFFRACTION (2.2 Å) |  | Cite: | Rational design of a novel, potent, and orally bioavailable cyclohexylamine DPP-4 inhibitor by application of molecular modeling and X-ray crystallography of sitagliptin Bioorg.Med.Chem.Lett., 17, 2007
 
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| 7XZN 
   
  |  | 
| 3MNN 
   
  | | A Ruthenium Antitumour Agent Forms Specific Histone Protein Adducts in the Nucleosome Core |  | Descriptor: | 1,3,5-triaza-7-phosphatricyclo[3.3.1.1~3,7~]decane, 1-methyl-4-(1-methylethyl)benzene, DNA (145-MER), ... |  | Authors: | Ong, M.S,  Davey, C.A. |  | Deposit date: | 2010-04-22 |  | Release date: | 2011-04-06 |  | Last modified: | 2023-11-01 |  | Method: | X-RAY DIFFRACTION (2.5 Å) |  | Cite: | A ruthenium antimetastasis agent forms specific histone protein adducts in the nucleosome core Chemistry, 17, 2011
 
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| 7XYJ 
   
  | | Structure of WSSV thymidylate synthase in complex with dUMP |  | Descriptor: | 2'-DEOXYURIDINE 5'-MONOPHOSPHATE, 2-[BIS-(2-HYDROXY-ETHYL)-AMINO]-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, PENTAETHYLENE GLYCOL, ... |  | Authors: | Ma, Q,  Liu, C,  Zang, K. |  | Deposit date: | 2022-06-01 |  | Release date: | 2023-06-07 |  | Last modified: | 2023-11-29 |  | Method: | X-RAY DIFFRACTION (2.275 Å) |  | Cite: | Structure of WSSV thymidylate synthase in complex with dUMP To Be Published
 
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| 5EVB 
   
  | | Crystal structure of the metallo-beta-lactamase L1 in complex with the bisthiazolidine inhibitor D-CS319 |  | Descriptor: | (3S,5S,7aR)-5-(sulfanylmethyl)tetrahydro[1,3]thiazolo[4,3-b][1,3]thiazole-3-carboxylic acid, Metallo-beta-lactamase L1, SULFATE ION, ... |  | Authors: | Hinchliffe, P,  Spencer, J. |  | Deposit date: | 2015-11-19 |  | Release date: | 2016-06-01 |  | Last modified: | 2024-11-13 |  | Method: | X-RAY DIFFRACTION (1.841 Å) |  | Cite: | Cross-class metallo-beta-lactamase inhibition by bisthiazolidines reveals multiple binding modes. Proc.Natl.Acad.Sci.USA, 113, 2016
 
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| 7RJQ 
   
  | | Crystal structure of human Bromodomain containing protein 4 (BRD4) in complex with ILF3 |  | Descriptor: | 1,2-ETHANEDIOL, Bromodomain-containing protein 4, CHLORIDE ION, ... |  | Authors: | Fedorov, E,  Islam, K,  Ghosh, A. |  | Deposit date: | 2021-07-21 |  | Release date: | 2022-08-03 |  | Last modified: | 2024-11-20 |  | Method: | X-RAY DIFFRACTION (1.72 Å) |  | Cite: | Uncovering the Bromodomain Interactome using Site-Specific Azide-Acetyllysine Photochemistry, Proteomic Profiling and Structural Characterization To Be Published
 
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| 3MJ5 
   
  | | Severe Acute Respiratory Syndrome-Coronavirus Papain-Like Protease Inhibitors: Design, Synthesis, Protein-Ligand X-ray Structure and Biological Evaluation |  | Descriptor: | N-(1,3-benzodioxol-5-ylmethyl)-1-[(1R)-1-naphthalen-1-ylethyl]piperidine-4-carboxamide, Replicase polyprotein 1a, ZINC ION |  | Authors: | Mesecar, A.D,  Ratia, K.M,  Pegan, S.D. |  | Deposit date: | 2010-04-12 |  | Release date: | 2010-06-30 |  | Last modified: | 2024-11-20 |  | Method: | X-RAY DIFFRACTION (2.63 Å) |  | Cite: | Severe acute respiratory syndrome coronavirus papain-like novel protease inhibitors: design, synthesis, protein-ligand X-ray structure and biological evaluation J.Med.Chem., 53, 2010
 
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| 5EVD 
   
  | | Crystal structure of the metallo-beta-lactamase L1 in complex with the bisthiazolidine inhibitor D-VC26 |  | Descriptor: | (3S,5S,7aR)-2,2-dimethyl-5-(sulfanylmethyl)tetrahydro[1,3]thiazolo[4,3-b][1,3]thiazole-3-carboxylic acid, Metallo-beta-lactamase L1, SULFATE ION, ... |  | Authors: | Hinchliffe, P,  Spencer, J. |  | Deposit date: | 2015-11-19 |  | Release date: | 2016-06-01 |  | Last modified: | 2024-11-20 |  | Method: | X-RAY DIFFRACTION (1.8 Å) |  | Cite: | Cross-class metallo-beta-lactamase inhibition by bisthiazolidines reveals multiple binding modes. Proc.Natl.Acad.Sci.USA, 113, 2016
 
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| 4N66 
   
  | | Thermolysin in complex with UBTLN37 |  | Descriptor: | CALCIUM ION, DIMETHYL SULFOXIDE, GLYCEROL, ... |  | Authors: | Krimmer, S.G,  Heine, A,  Klebe, G. |  | Deposit date: | 2013-10-11 |  | Release date: | 2014-04-02 |  | Last modified: | 2023-09-20 |  | Method: | X-RAY DIFFRACTION (1.44 Å) |  | Cite: | Methyl, Ethyl, Propyl, Butyl: Futile But Not for Water, as the Correlation of Structure and Thermodynamic Signature Shows in a Congeneric Series of Thermolysin Inhibitors. Chemmedchem, 4, 2014
 
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