| 7YJM 
   
  | | Cryo-EM structure of the monomeric atSPT-ORM1 complex |  | Descriptor: | Long chain base biosynthesis protein 2a, N-[(2S,3R,4E)-1,3-dihydroxyoctadec-4-en-2-yl]tetracosanamide, ORMDL family protein, ... |  | Authors: | Xie, T,  Liu, P,  Gong, X. |  | Deposit date: | 2022-07-20 |  | Release date: | 2023-04-05 |  | Last modified: | 2025-07-02 |  | Method: | ELECTRON MICROSCOPY (3.2 Å) |  | Cite: | Mechanism of sphingolipid homeostasis revealed by structural analysis of Arabidopsis SPT-ORM1 complex. Sci Adv, 9, 2023
 
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| 7YJK 
   
  | | Cryo-EM structure of the dimeric atSPT-ORM1 complex |  | Descriptor: | Long chain base biosynthesis protein 1, Long chain base biosynthesis protein 2a, N-[(2S,3R,4E)-1,3-dihydroxyoctadec-4-en-2-yl]tetracosanamide, ... |  | Authors: | Xie, T,  Liu, P,  Gong, X. |  | Deposit date: | 2022-07-20 |  | Release date: | 2023-04-05 |  | Last modified: | 2025-06-25 |  | Method: | ELECTRON MICROSCOPY (3.2 Å) |  | Cite: | Mechanism of sphingolipid homeostasis revealed by structural analysis of Arabidopsis SPT-ORM1 complex. Sci Adv, 9, 2023
 
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| 5EYR 
   
  | | Structure of Transcriptional Regulatory Repressor Protein - EthR from Mycobacterium Tuberculosis in complex with compound 5 at 1.57A resolution |  | Descriptor: | 3-[1-[4-(methylaminomethyl)phenyl]piperidin-4-yl]-1-pyrrolidin-1-yl-propan-1-one, EthR |  | Authors: | Surade, S,  Blaszczyk, M,  Nikiforov, P.O,  Abell, C,  Blundell, T.L. |  | Deposit date: | 2015-11-25 |  | Release date: | 2016-02-03 |  | Last modified: | 2024-01-10 |  | Method: | X-RAY DIFFRACTION (1.57 Å) |  | Cite: | A fragment merging approach towards the development of small molecule inhibitors of Mycobacterium tuberculosis EthR for use as ethionamide boosters. Org.Biomol.Chem., 14, 2016
 
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| 2OZR 
   
  | | MMP13 Catalytic Domain Complexed with 4-{[1-methyl-2,4-dioxo-6-(3-phenylprop-1-yn-1-yl)-1,4-dihydroquinazolin-3(2H)-yl]methyl}benzoic acid |  | Descriptor: | 4-{[1-METHYL-2,4-DIOXO-6-(3-PHENYLPROP-1-YN-1-YL)-1,4-DIHYDROQUINAZOLIN-3(2H)-YL]METHYL}BENZOIC ACID, ACETOHYDROXAMIC ACID, CALCIUM ION, ... |  | Authors: | Johnson, A.R,  Pavlovsky, A.G,  Ortwine, D.F,  Prior, F,  Man, C.-F,  Bornemeier, D.A,  Banotai, C.A,  Mueller, W.T,  McConnell, P,  Yan, C.H,  Baragi, V,  Lesch, C,  Roark, W.H,  Lie, J.J,  Fasquelle, V,  Wilson, M,  Robertson, D,  Datta, K,  Guzman, R,  Han, H.-K,  Dyer, R.D. |  | Deposit date: | 2007-02-27 |  | Release date: | 2007-07-24 |  | Last modified: | 2024-03-13 |  | Method: | X-RAY DIFFRACTION (2.3 Å) |  | Cite: | Discovery and characterization of a novel inhibitor of matrix metalloprotease-13 that reduces cartilage damage in vivo without joint fibroplasia side effects. J.Biol.Chem., 282, 2007
 
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| 1ZH0 
   
  | | Crystal Structure of L-3-(2-napthyl)alanine-tRNA synthetase in complex with L-3-(2-napthyl)alanine |  | Descriptor: | 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, BETA-(2-NAPHTHYL)-ALANINE, Tyrosyl-tRNA synthetase |  | Authors: | Turner, J.M,  Graziano, J,  Spraggon, G,  Schultz, P.G. |  | Deposit date: | 2005-04-22 |  | Release date: | 2006-04-04 |  | Last modified: | 2024-02-14 |  | Method: | X-RAY DIFFRACTION (1.9 Å) |  | Cite: | Structural plasticity of an aminoacyl-tRNA synthetase active site Proc.Natl.Acad.Sci.Usa, 103, 2006
 
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| 2P9H 
   
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| 5EXN 
   
  | | FACTOR XIA (C500S [C122S]) IN COMPLEX WITH THE INHIBITOR methyl ~{N}-[4-[2-[(1~{S})-1-[[(~{E})-3-[5-chloranyl-2-(1,2,3,4-tetrazol-1-yl)phenyl]prop-2-enoyl]amino]-2-phenyl-ethyl]pyridin-4-yl]phenyl]carbamate |  | Descriptor: | 2-acetamido-2-deoxy-beta-D-glucopyranose, Coagulation factor XIa light chain, methyl ~{N}-[4-[2-[(1~{S})-1-[[(~{E})-3-[5-chloranyl-2-(1,2,3,4-tetrazol-1-yl)phenyl]prop-2-enoyl]amino]-2-phenyl-ethyl]pyridin-4-yl]phenyl]carbamate |  | Authors: | Sheriff, S. |  | Deposit date: | 2015-11-23 |  | Release date: | 2016-04-13 |  | Last modified: | 2024-11-20 |  | Method: | X-RAY DIFFRACTION (1.49 Å) |  | Cite: | Orally bioavailable pyridine and pyrimidine-based Factor XIa inhibitors: Discovery of the methyl N-phenyl carbamate P2 prime group Bioorg.Med.Chem., 24, 2016
 
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| 1ZLR 
   
  | | Factor XI catalytic domain complexed with 2-guanidino-1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethyl nicotinate |  | Descriptor: | (1R)-2-{[AMINO(IMINO)METHYL]AMINO}-1-{4-[(4R)-4-(HYDROXYMETHYL)-1,3,2-DIOXABOROLAN-2-YL]PHENYL}ETHYL NICOTINATE, Coagulation factor XI, GLYCEROL, ... |  | Authors: | Lazarova, T.I,  Jin, L,  Rynkiewicz, M,  Gorga, J.C,  Bibbins, F,  Meyers, H.V,  Babine, R,  Strickler, J. |  | Deposit date: | 2005-05-09 |  | Release date: | 2006-05-09 |  | Last modified: | 2024-11-06 |  | Method: | X-RAY DIFFRACTION (2.5 Å) |  | Cite: | Synthesis and in vitro biological evaluation of aryl boronic acids as potential inhibitors of factor XIa. Bioorg.Med.Chem.Lett., 16, 2006
 
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| 7YIS 
   
  | | Crystal structure of N-terminal PH domain of ARAP3 protein in complex with inositol 1,3,4,5-tetrakisphosphate |  | Descriptor: | (2R)-3-{[(S)-{[(2S,3R,5S,6S)-2,6-DIHYDROXY-3,4,5-TRIS(PHOSPHONOOXY)CYCLOHEXYL]OXY}(HYDROXY)PHOSPHORYL]OXY}-2-(1-HYDROXY BUTOXY)PROPYL BUTYRATE, Arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 3 |  | Authors: | Zhang, Y.J,  Liu, Y.R,  Wu, B. |  | Deposit date: | 2022-07-18 |  | Release date: | 2023-05-03 |  | Last modified: | 2023-11-29 |  | Method: | X-RAY DIFFRACTION (3.3 Å) |  | Cite: | Structural Insights Uncover the Specific Phosphoinositide Recognition by the PH1 Domain of Arap3. Int J Mol Sci, 24, 2023
 
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| 1YVN 
   
  | | THE YEAST ACTIN VAL 159 ASN MUTANT COMPLEX WITH HUMAN GELSOLIN SEGMENT 1. |  | Descriptor: | ADENOSINE-5'-TRIPHOSPHATE, CALCIUM ION, MAGNESIUM ION, ... |  | Authors: | Vorobiev, S.M,  Belmont, L.D,  Drubin, D.G,  Almo, S.C. |  | Deposit date: | 1999-03-23 |  | Release date: | 2000-03-23 |  | Last modified: | 2023-08-23 |  | Method: | X-RAY DIFFRACTION (2.1 Å) |  | Cite: | Crystal structure of yeast actin V159N mutant To be Published
 
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| 1ZJB 
   
  | | Crystal structure of the trehalulose synthase MutB from Pseudomonas mesoacidophila MX-45 (monoclinic form) |  | Descriptor: | 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, CALCIUM ION, Trehalulose synthase |  | Authors: | Ravaud, S,  Robert, X,  Haser, R,  Aghajari, N. |  | Deposit date: | 2005-04-28 |  | Release date: | 2006-10-17 |  | Last modified: | 2023-08-23 |  | Method: | X-RAY DIFFRACTION (1.8 Å) |  | Cite: | Expression, purification, crystallization and preliminary X-ray crystallographic studies of the trehalulose synthase MutB from Pseudomonas mesoacidophila MX-45. Acta Crystallogr.,Sect.F, 61, 2005
 
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| 1ZKO 
   
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| 5F1J 
   
  | | Structure of Transcriptional Regulatory Repressor Protein - EthR from Mycobacterium Tuberculosis in complex with compound 1 at 1.63A resolution |  | Descriptor: | 3-cyclopentyl-1-pyrrolidin-1-yl-propan-1-one, HTH-type transcriptional regulator EthR |  | Authors: | Surade, S,  Blaszczyk, M,  Nikiforov, P.O,  Abell, C,  Blundell, T.L. |  | Deposit date: | 2015-11-30 |  | Release date: | 2016-02-03 |  | Last modified: | 2024-01-10 |  | Method: | X-RAY DIFFRACTION (1.631 Å) |  | Cite: | A fragment merging approach towards the development of small molecule inhibitors of Mycobacterium tuberculosis EthR for use as ethionamide boosters. Org.Biomol.Chem., 14, 2016
 
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| 7R5C 
   
  | | Structure of E.coli Class 2 L-asparaginase EcAIII, mutant RDM1-29 (G206C, R207S, D210L, S211V) |  | Descriptor: | 1,2-ETHANEDIOL, 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, Isoaspartyl peptidase, ... |  | Authors: | Barciszewski, J,  Imiolczyk, B,  Loch, J.I,  Jaskolski, M. |  | Deposit date: | 2022-02-10 |  | Release date: | 2022-07-13 |  | Last modified: | 2024-01-31 |  | Method: | X-RAY DIFFRACTION (2.2 Å) |  | Cite: | Structural and biophysical studies of new L-asparaginase variants: lessons from random mutagenesis of the prototypic Escherichia coli Ntn-amidohydrolase. Acta Crystallogr D Struct Biol, 78, 2022
 
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| 7RKL 
   
  | | Structure of Nicotinamide N-Methyltransferase (NNMT) in complex with II399 (P1 space group) |  | Descriptor: | 3-[3-(acetyl{[(1R,2R,3S,4R)-4-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-2,3-dihydroxycyclopentyl]methyl}amino)prop-1-yn-1-yl]benzamide, NNMT protein, SULFATE ION |  | Authors: | Yadav, R,  Noinaj, N,  Iyamu, I.D,  Huang, R. |  | Deposit date: | 2021-07-22 |  | Release date: | 2022-07-20 |  | Last modified: | 2023-10-18 |  | Method: | X-RAY DIFFRACTION (2.08 Å) |  | Cite: | Exploring Unconventional SAM Analogues To Build Cell-Potent Bisubstrate Inhibitors for Nicotinamide N-Methyltransferase. Angew.Chem.Int.Ed.Engl., 61, 2022
 
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| 9FXW 
   
  | | 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 (1.95 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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| 5EW0 
   
  | | Crystal structure of the metallo-beta-lactamase Sfh-I in complex with the bisthiazolidine inhibitor L-CS319 |  | Descriptor: | (3R,5R,7aS)-5-(sulfanylmethyl)tetrahydro[1,3]thiazolo[4,3-b][1,3]thiazole-3-carboxylic acid, Beta-lactamase, ZINC ION |  | Authors: | Hinchliffe, P,  Tooke, C.L,  Spencer, J. |  | Deposit date: | 2015-11-20 |  | Release date: | 2016-06-01 |  | Last modified: | 2024-01-10 |  | Method: | X-RAY DIFFRACTION (1.3 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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| 7YL5 
   
  | | Cell surface protein YwfG protein complexed with mannose |  | Descriptor: | CALCIUM ION, GRAM_POS_ANCHORING domain-containing protein, SULFATE ION, ... |  | Authors: | Tsuchiya, W,  Fujimoto, Z,  Suzuki, C. |  | Deposit date: | 2022-07-25 |  | Release date: | 2023-06-07 |  | Last modified: | 2023-11-29 |  | Method: | X-RAY DIFFRACTION (3 Å) |  | Cite: | Cell-surface protein YwfG of Lactococcus lactis binds to alpha-1,2-linked mannose. Plos One, 18, 2023
 
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| 4MXW 
   
  | | Structure of heterotrimeric lymphotoxin LTa1b2 bound to lymphotoxin beta receptor LTbR and anti-LTa Fab |  | Descriptor: | Lymphotoxin-alpha, Lymphotoxin-beta, Tumor necrosis factor receptor superfamily member 3, ... |  | Authors: | Sudhamsu, J,  Yin, J.P,  Hymowitz, S.G. |  | Deposit date: | 2013-09-26 |  | Release date: | 2013-11-13 |  | Last modified: | 2024-11-20 |  | Method: | X-RAY DIFFRACTION (3.6 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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| 7YL4 
   
  | | Cell surface protein YwfG protein (apo form) |  | Descriptor: | CALCIUM ION, GRAM_POS_ANCHORING domain-containing protein, SULFATE ION |  | Authors: | Tsuchiya, W,  Fujimoto, Z,  Suzuki, C. |  | Deposit date: | 2022-07-25 |  | Release date: | 2023-06-07 |  | Last modified: | 2023-11-29 |  | Method: | X-RAY DIFFRACTION (2.5 Å) |  | Cite: | Cell-surface protein YwfG of Lactococcus lactis binds to alpha-1,2-linked mannose. Plos One, 18, 2023
 
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| 7RJR 
   
  | | Crystal structure of human Bromodomain containing protein 4 (BRD4) in complex with BCLTF1 |  | Descriptor: | 1,2-ETHANEDIOL, Bcl-2-associated transcription factor 1, Bromodomain-containing protein 4, ... |  | Authors: | Fedorov, E,  Islam, K,  Ghosh, A. |  | Deposit date: | 2021-07-21 |  | Release date: | 2022-08-03 |  | Last modified: | 2024-10-09 |  | Method: | X-RAY DIFFRACTION (1.45 Å) |  | Cite: | Uncovering the Bromodomain Interactome using Site-Specific Azide-Acetyllysine Photochemistry, Proteomic Profiling and Structural Characterization To Be Published
 
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| 7RJK 
   
  | | Crystal structure of human Bromodomain containing protein 3 (BRD3) in complex with hnRNPK |  | Descriptor: | 1,2-ETHANEDIOL, Bromodomain-containing protein 3, GLYCEROL, ... |  | Authors: | Fedorov, E,  Islam, K,  Ghosh, A. |  | Deposit date: | 2021-07-21 |  | Release date: | 2022-08-03 |  | Last modified: | 2024-11-06 |  | Method: | X-RAY DIFFRACTION (1.85 Å) |  | Cite: | Uncovering the Bromodomain Interactome using Site-Specific Azide-Acetyllysine Photochemistry, Proteomic Profiling and Structural Characterization Biorxiv, 2021
 
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| 1ZI8 
   
  | | Crystal Structure Analysis of the dienelactone hydrolase mutant(E36D, C123S, A134S, S208G, A229V, K234R)- 1.4 A |  | Descriptor: | Carboxymethylenebutenolidase, GLYCEROL, SULFATE ION |  | Authors: | Kim, H.-K,  Liu, J.-W,  Carr, P.D,  Ollis, D.L. |  | Deposit date: | 2005-04-27 |  | Release date: | 2005-07-05 |  | Last modified: | 2023-10-25 |  | Method: | X-RAY DIFFRACTION (1.4 Å) |  | Cite: | Following directed evolution with crystallography: structural changes observed in changing the substrate specificity of dienelactone hydrolase. Acta Crystallogr.,Sect.D, 61, 2005
 
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| 7RJN 
   
  | | Crystal structure of human bromodomain containing protein 3 (BRD3) in complex with BCLTF1 |  | Descriptor: | 1,2-ETHANEDIOL, Bcl-2-associated transcription factor 1, Bromodomain-containing protein 3 |  | Authors: | Fedorov, E,  Islam, K,  Ghosh, A. |  | Deposit date: | 2021-07-21 |  | Release date: | 2022-08-03 |  | Last modified: | 2024-11-06 |  | Method: | X-RAY DIFFRACTION (1.95 Å) |  | Cite: | Uncovering the Bromodomain Interactome using Site-Specific Azide-Acetyllysine Photochemistry, Proteomic Profiling and Structural Characterization Biorxiv, 2021
 
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| 4N9E 
   
  | | Fragment-based Design of 3-Aminopyridine-derived Amides as Potent Inhibitors of Human Nicotinamide Phosphoribosyltransferase (NAMPT) |  | Descriptor: | 1,2-ETHANEDIOL, 1-[(1-benzoylpiperidin-4-yl)methyl]-N-(pyridin-3-yl)-1H-benzimidazole-5-carboxamide, 2,3-DIHYDROXY-1,4-DITHIOBUTANE, ... |  | Authors: | Dragovich, P.S,  Zhao, G,  Baumeister, T,  Bravo, B,  Giannetti, A.M,  Ho, Y,  Hua, R,  Li, G,  Liang, X,  O'Brien, T,  Skelton, N.J,  Wang, C,  Zhao, Q,  Oh, A,  Wang, W,  Wang, Y,  Xiao, Y,  Yuen, P,  Zak, M,  Zheng, X. |  | Deposit date: | 2013-10-20 |  | Release date: | 2014-02-19 |  | Last modified: | 2024-02-28 |  | Method: | X-RAY DIFFRACTION (1.72 Å) |  | Cite: | Fragment-based design of 3-aminopyridine-derived amides as potent inhibitors of human nicotinamide phosphoribosyltransferase (NAMPT). Bioorg.Med.Chem.Lett., 24, 2014
 
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