 | 3POO | Human cAMP-dependent protein kinase in complex with an inhibitor | View ligand
View ligand
| H. Köster
|
 | 3PMY | Endothiapepsin in complex with a fragment | View ligand
| H. Köster
|
 | 3PMU | Endothiapepsin in complex with a fragment | View ligand
| H. Köster
|
 | 3PM4 | Endothiapepsin in complex with a fragment | View ligand
| H. Köster
|
 | 3PLL | Endothiapepsin in complex with a fragment | View ligand
| H. Köster
|
 | 3PLD | Endothiapepsin in complex with a fragment | View ligand
| H. Köster
|
 | 3PI0 | Endothiapepsin in complex with a fragment | View ligand
| H. Köster
|
 | 3P17 | Thrombin Inhibition by Pyridin Derivatives | View ligand
| A. Biela
|
 | 3PRS | Endothiapepsin in complex with ritonavir | View ligand
| H. Köster
|
 | 3PGI | Endothiapepsin in complex with a fragment | View ligand
| H. Köster
|
 | 3PCZ | Endothiapepsin in complex with benzamidine | View ligand
| H. Köster
|
 | 3PCW | Endothiapepsin in complex with a fragment | View ligand
| H. Köster
|
 | 3PBZ | Endothiapepsin in complex with a fragment | View ligand
| H. Köster
|
 | 3PBD | Endothiapepsin in complex with a fragment | View ligand
| H. Köster
|
 | 3PB5 | Endothiapepsin in complex with a fragment | View ligand
| H. Köster
|
 | 3P0M | Human cAMP-dependent protein kinase in complex with an inhibitor | View ligand
| H. Köster
|
 | 3OXT | Human cAMP-dependent protein kinase in complex with an inhibitor | View ligand
| H. Köster
|
 | 3OWP | Human cAMP-dependent protein kinase in complex with an inhibitor | View ligand
| H. Köster
|
 | 3OVV | Human cAMP-dependent protein kinase in complex with an inhibitor | View ligand
View ligand
| H. Köster
|
 | 3OOG | Human cAMP-dependent protein kinase in complex with a small fragment | View ligand
| H. Köster
|
 | 3P2V | Novel Benzothiazepine Inhibitor in Complex with human Aldose Reductase | View ligand
| C. Koch
|
 | 3ONC | Bond breakage and relocation of a covalently bound bromine of IDD594 in a complex with hAR T113A mutant after moderate radiation dose | View ligand
| C. Koch
|
 | 3ONB | Bond breakage and relocation of a covalently bound bromine of IDD594 in a complex with hAR T113A mutant after extensive radiation dose | View ligand
| C. Koch
|
 | 3NX8 | Human cAMP dependent protein kinase in complex with phenol | View ligand
| H. Köster
|
 | 3M2Z | Fragment tethered to Carbonic Anhydrase II H64C mutant | View ligand
| J. Schulze Wischeler
|
 | 3NN7 | Crystal structure of Thermolysin in complex with 2-bromoacetate | View ligand
| J. Behnen
|
 | 3N9W | Crystal structure of 2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase (IspD) in complex with 1,2-Propanediol | View ligand
View ligand
| J. Behnen
|
 | 3N4A | Crystal structure of D-Xylose Isomerase in complex with S-1,2-Propandiol | View ligand
| J. Behnen
|
 | 3N21 | Crystal structure of Thermolysin in complex with S-1,2-Propandiol | View ligand
| J. Behnen
|
 | 3M5T | Fragment tethered to Carbonic Anhydrase II H64C mutant | View ligand
| J. Schulze Wischeler
|
 | 3M5S | Carbonic Anhydrase II mutant H64C in complex with carbonate | View ligand
| J. Schulze Wischeler
|
 | 3M2Y | Carbonic Anhydrase II in complex with novel sulfonamide inhibitor | View ligand
| J. Schulze Wischeler
|
 | 3M2X | Carbonic Anhydrase II in complex with novel sulfonamide inhibitor | View ligand
| J. Schulze Wischeler
|
 | 3M1W | Carbonic Anhyrdase II mutant W5CH64C with closed disulfide bond in complex with sulfate | View ligand
| J. Schulze Wischeler
|
 | 3M1Q | Carbonic Anhydrase II mutant W5C-H64C with opened disulfide bond | | J. Schulze Wischeler
|
 | 3M14 | Carbonic Anhydrase II in complex with novel sulfonamide inhibitor | View ligand
| J. Schulze Wischeler
|
 | 3M04 | Carbonic Anhydrase II in complex with novel sulfonamide inhibitor | View ligand
| J. Schulze Wischeler
|
 | 3LZY | Crystal structure of Endothiapesin in complex with Xenon | View ligand
| J. Behnen
|
 | 3KNE | Carbonic Anhydrase II H64C mutant in complex with an in situ formed triazole | View ligand
| J. Schulze Wischeler
|
 | 3MSN | Crystal structure of Thermolysin in complex with N-methylurea | View ligand
| J. Behnen
|
 | 3MSF | Crystal structure of Thermolysin in complex with Urea | View ligand
| J. Behnen
|
 | 3MSA | Crystal structure of Thermolysin in complex with 3-Bromophenol | View ligand
| J. Behnen
|
 | 3MS3 | Crystal structure of Thermolysin in complex with Aniline | View ligand
| J. Behnen
|
 | 3MC5 | Human Aldose Reductase mutant T113V in complex with IDD393 crystallized in spacegroup P1 | View ligand
| C. Koch
|
 | 3MB9 | Human Aldose Reductase mutant T113A complexed with Zopolrestat | View ligand
| C. Koch
|
 | 3M64 | Human aldose reductase mutant T113V complexed with IDD393 | View ligand
| C. Koch
|
 | 3M3D | Crystal structure of Acetylcholinesterase in complex with Xenon | View ligand
| J. Behnen
|
 | 3M0I | Human Aldose Reductase mutant T113V in complex with Zopolrestat | View ligand
| C. Koch
|
 | 3LS7 | Crystal structure of Thermolysin in complex with Xenon | View ligand
| J. Behnen
|
 | 3LEN | Human Aldose Reductase mutant T113S complexed with Zopolrestat | View ligand
| C. Koch
|
 | 3M4H | Human Aldose Reductase mutant T113V complexed with IDD388 | View ligand
| C. Koch
|
 | 3LZ5 | Human aldose reductase mutant T113V complexed with IDD594 | View ligand
| C. Koch
|
 | 3LZ3 | Human aldose reductase mutant T113S complexed with IDD388 | View ligand
| C. Koch
|
 | 3LQL | Human Aldose Reductase mutant T113A complexed with IDD 594 | View ligand
| C. Koch
|
 | 3LQG | Human aldose reductase mutant T113A complexed with IDD388 | View ligand
| C. Koch
|
 | 3LEP | Human Aldose Reductase mutant T113C in complex with IDD388 | View ligand
| C. Koch
|
 | 3LD5 | Human aldose reductase mutant T113S complexed with IDD594 | View ligand
| C. Koch
|
 | 3LBO | Human aldose reductase mutant T113C complexed with IDD594 | View ligand
| C. Koch
|
 | 3M1K | Carbonic Anhydrase in complex with fragment | View ligand
| J. Schulze Wischeler
|
 | 3KIG | Mutant carbonic anhydrase II in complex with an azide and an alkyne | View ligand
View ligand
| J. Schulze Wischeler
|
 | 3LJO | Bovine trypsin in complex with UB-THR 11 | View ligand
| C. Gerlach
|
 | 3LJJ | Bovine trypsin in complex with UB-THR 10 | View ligand
| C. Gerlach
|
 | 3GFN | tRNA-guanine transglycosylase complexed with 2-{[2-(4-Morpholinyl)ethyl]amino}-1,7-dihydro-8H-imidazo[4,5-g]quinazolin-8-one | View ligand
| T. Ritschel
|
 | 3GEV | tRNA-guanine transglycosylase in complex with 2-[(2-Thienylmethyl)amino]-1,7-dihydro-8H-imidazo[4,5-g]quinazolin-8-one | View ligand
| T. Ritschel
|
 | 3FXS | Metal exchange in thermolysin | View ligand
| L. Englert
|
 | 3FXP | Thermolysin inhibition | View ligand
| L. Englert
|
 | 3FWD | Thermolysin inhibition | View ligand
| L. Englert
|
 | 3FVP | Thermolysin inhibition | View ligand
| L. Englert
|
 | 3FV4 | Thermolysin inhibition | View ligand
| L. Englert
|
 | 3FLF | Thermolysin inhibition | View ligand
| L. Englert
|
 | 3GE7 | tRNA-guanine transglycosylase in complex with 6-amino-4-{2-[(cyclopentylmethyl)amino]ethyl}-2-(methylamino)-1,7-dihydro-8H-imidazo[4,5-g]quinazolin-8-one | View ligand
| T. Ritschel
|
 | 3GC5 | tRNA-guanine transglycosylase in complex with 6-amino-4-(2-aminoethyl)-2-(methylamino)-1,7-dihydro-8H-imidazo[4,5-g]quinazolin-8-one | View ligand
| T. Ritschel
|
 | 3GC4 | tRNA-guanine transglycosylase in complex with inhibitor | View ligand
| T. Ritschel
|
 | 3FGD | Drugscore FP: Thermoylsin in complex with fragment. | View ligand
| L. Englert
|
 | 3FCQ | Thermolysin inhibition | View ligand
| H. Steuber
|
 | 3FBO | Metal exchange in Thermolysin | | L. Englert
|
 | 3FB0 | Metal exchange in thermolysin | | L. Englert
|
 | 3F2P | Thermolysin inhibition | View ligand
| L. Englert
|
 | 3F28 | Thermolysin inhibition | View ligand
| L. Englert
|
 | 3F68 | Thrombin Inhibition | View ligand
| B. Baum
|
 | 3EIM | Metal exchange in Thermolysin | | L. Englert
|
 | 3EOU | tRNA-guanine transglycosylase in complex with 6-amino-4-(2-hydroxyethyl)-2-(methylamino)-3,7-dihydro-8H-imidazo[4,5-g]quinazolin-8-one | View ligand
| T. Ritschel
|
 | 3EOS | tRNA-guanine transglycosylase in complex with 6-amino-4-{2-[(cyclohexylmethyl)amino]ethyl}-2-(methylamino)-1,7-dihydro-8H-imidazo[4,5-g]quinazolin-8-one | View ligand
| T. Ritschel
|
 | 3HFY | Mutant of tRNA-guanine transglycosylase (K52M) | | T. Ritschel
|
 | 3EQ0 | Thrombin Inhibitor | View ligand
| B. Baum
|
 | 2ZQ2 | Exploring trypsin S3 pocket | View ligand
| T. Brandt
|
 | 2ZQ1 | Exploring trypsin S3 pocket | View ligand
| T. Brandt
|
 | 3DUX | Understanding Thrombin Inhibition | View ligand
| B. Baum
|
 | 3DT0 | Understanding Thrombin Inhibition | View ligand
| B. Baum
|
 | 3DHK | Bisphenylic Thrombin Inhibitors | View ligand
| B. Baum
|
 | 3D49 | Thrombin Inhibition | View ligand
| B. Baum
|
 | 2ZO3 | Bisphenylic Thrombin Inhibitors | View ligand
| B. Baum
|
 | 2ZNK | Thrombin Inhibition | View ligand
| B. Baum
|
 | 3DN5 | Aldose Reductase in complex with novel biarylic inhibitor | View ligand
| H. Steuber
|
 | 3CKT | HIV-1 protease in complex with a dimethylallyl decorated pyrrolidine based inhibitor (orthorombic space group) | View ligand
| J. Böttcher
|
 | 2ZHW | Exploring thrombin S3 pocket | View ligand
| T. Brandt
|
 | 2ZHF | Exploring thrombin S3 pocket | View ligand
| T. Brandt
|
 | 2ZHE | Exploring thrombin S3 pocket | View ligand
| T. Brandt
|
 | 2ZHD | Exploring trypsin S3 pocket | View ligand
| T. Brandt
|
 | 3C2Z | tRNA-Guanine Transglycosylase (TGT) in complex with 6-Amino-2-[(thiophen-2-ylmethyl)-amino]-1,7-dihydro-imidazo[4,5-g]quinazolin-8-one | View ligand
| T. Ritschel
|
 | 3C2Y | tRNA-Guanine Transglycosylase (TGT) in complex with 6-Amino-2-methyl-1,7-dihydro-imidazo[4,5-g]quinazolin-8-one | View ligand
| T. Ritschel
|
 | 3C2N | tRNA-Guanine Transglycosylase (TGT) in complex with 6-Amino-2-(2-morpholin-4-yl-ethylamino)-1,7-dihydro-imidazo[4,5-g]quinazolin-8-one | View ligand
| T. Ritschel
|
 | 2ZGA | HIV-1 protease in complex with a dimethylallyl decorated pyrrolidine based inhibitor (hexagonal space group) | View ligand
| J. Böttcher
|
 | 2ZG0 | Exploring thrombin S3 pocket | View ligand
| T. Brandt
|
 | 2ZIQ | Thrombin Inhibition | View ligand
| B. Baum
|
 | 2ZI2 | Thrombin Inhibition | View ligand
| B. Baum
|
 | 2ZHQ | Thrombin Inhibition | View ligand
| B. Baum
|
 | 2ZFT | Exploring trypsin S3 pocket | View ligand
| T. Brandt
|
 | 2ZFS | Exploring trypsin S3 pocket | View ligand
| T. Brandt
|
 | 2ZFR | Exploring thrombin S3 pocket | View ligand
| T. Brandt
|
 | 2ZFQ | Exploring thrombin S3 pocket | View ligand
| T. Brandt
|
 | 3BLO | TGT mutant in complex with queuine | View ligand
| N. Tidten
|
 | 3BLL | TGT mutant in complex with Boc-preQ1 | View ligand
| N. Tidten
|
 | 3BLD | tRNA guanine transglycosylase V233G mutant preQ1 complex structure | View ligand
| N. Tidten
|
 | 3BL3 | tRNA guanine transglycosylase V233G mutant apo structure | | N. Tidten
|
 | 2ZGX | Thrombin Inhibition | View ligand
| B. Baum
|
 | 2ZGB | Thrombin Inhibition | View ligand
| B. Baum
|
 | 2ZFP | Thrombin Inibition | View ligand
| B. Baum
|
 | 2ZFF | Exploring Thrombin S1-pocket | View ligand
| B. Baum
|
 | 3BHE | HIV-1 protease in complex with a three armed pyrrolidine derivative | View ligand
| J. Böttcher
|
 | 3BAZ | Structure of hydroxyphenylpyruvate reductase from coleus blumei in complex with NADP+ | View ligand
| V. Janiak
|
 | 3BA1 | Structure of hydroxyphenylpyruvate reductase from coleus blumei | | V. Janiak
|
 | 2ZF0 | Exploring Thrombin S1 Pocket | View ligand
| B. Baum
|
 | 2ZDV | Exploring Thrombin S1 pocket | View ligand
| B. Baum
|
 | 2ZDA | Exploring Thrombin S1 pocket | View ligand
| B. Baum
|
 | 2ZC9 | Thrombin in complex with Inhibitor | View ligand
| B. Baum
|
 | 2ZDN | Exploring trypsin S3 pocket | View ligand
| T. Brandt
|
 | 2ZDM | Exploring trypsin S3 pocket | View ligand
| T. Brandt
|
 | 2ZDL | Exploring Trypsin S3 pocket | View ligand
| T. Brandt
|
 | 2ZDK | Exploring Trypsin S3 Pocket | View ligand
| T. Brandt
|
 | 3EGK | KNOBLE Inhibitor | View ligand
| B. Baum
|
 | 2R43 | I50V HIV-1 protease in complex with an amino decorated pyrrolidine-based inhibitor | View ligand
| J. Böttcher
|
 | 3BGC | HIV-1 protease in complex with a benzyl decorated oligoamine | View ligand
| J. Böttcher
|
 | 3BGB | HIV-1 protease in complex with a isobutyl decorated oligoamine | View ligand
| J. Böttcher
|
 | 3BC4 | I84V HIV-1 protease in complex with a pyrrolidine diester | View ligand
| J. Böttcher
|
 | 2R3W | I84V HIV-1 protease in complex with a amino decorated pyrrolidine-based inhibitor | View ligand
| J. Böttcher
|
 | 2R3T | I50V HIV-1 protease mutant in complex with a carbamoyl decorated pyrrolidine-based inhibitor | View ligand
| J. Böttcher
|
 | 2R38 | I84V HIV-1 protease mutant in complex with a carbamoyl decorated pyrrolidine-based inhibitor | View ligand
| J. Böttcher
|
 | 2Z7K | tRNA-Guanine transglycosylase (TGT) in complex with 2-Amino-lin-Benzoguanine | View ligand
| T. Ritschel
|
 | 2QAE | Crystal Structure Analysis of Trypanosoma cruzi Lipoamide dehydrogenase | View ligand
| C. Werner
|
 | 2QNQ | HIV-1 Protease in complex with a chloro decorated pyrrolidine-based inhibitor | View ligand
| J. Böttcher
|
 | 2QNP | HIV-1 Protease in complex with a iodo decorated pyrrolidine-based inhibitor | View ligand
| J. Böttcher
|
 | 2QNN | HIV-1 protease in complex with a multiple decorated pyrrolidine-based inhibitor | View ligand
| J. Böttcher
|
 | 2PWR | HIV-1 protease in complex with a carbamoyl decorated pyrrolidine-based inhibitor | View ligand
| J. Böttcher
|
 | 2PWC | HIV-1 protease in complex with a amino decorated pyrrolidine-based inhibitor | View ligand
| J. Böttcher
|
 | 2PQZ | HIV-1 Protease in complex with a pyrrolidine-based inhibitor | View ligand
| J. Böttcher
|
 | 2PDY | Human aldose reductase double mutant S302R-C303D complexed with fidarestat | View ligand
| H. Steuber
|
 | 2PDX | Human aldose reductase double mutant S302R-C303D complexed with zopolrestat | View ligand
| H. Steuber
|
 | 2PDW | Human aldose reductase mutant C303D complexed with fidarestat | View ligand
| H. Steuber
|
 | 2PDU | Human aldose reductase mutant C303D complexed with IDD393 | View ligand
| H. Steuber
|
 | 2PDQ | Human aldose reductase mutant C303D complexed with uracil-type inhibitor | View ligand
| H. Steuber
|
 | 2PDP | Human aldose reductase mutant S302R complexed with IDD 393 | View ligand
| H. Steuber
|
 | 2PDN | Human aldose reductase mutant S302R complexed with uracil-type inhibitor | View ligand
| H. Steuber
|
 | 2PDM | Human aldose reductase mutant S302R complexed with zopolrestat | View ligand
| H. Steuber
|
 | 2PDL | Human aldose reductase mutant L301M complexed with tolrestat | View ligand
| H. Steuber
|
 | 2PDK | Human aldose reductase mutant L301M complexed with sorbinil | View ligand
| H. Steuber
|
 | 2PDJ | Human aldose reductase mutant L300A complexed with IDD393 | View ligand
| H. Steuber
|
 | 2PDI | Human aldose reductase mutant L300A complexed with zopolrestat at 1.55 A | View ligand
| H. Steuber
|
 | 2PDH | Human aldose reductase mutant L300P complexed with uracil-type inhibitor at 1.45 A | View ligand
| H. Steuber
|
 | 2PDG | Human aldose reductase with uracil-type inhibitor at 1.42A | View ligand
| H. Steuber
|
 | 2PDF | Human aldose reductase mutant L300P complexed with zopolrestat | View ligand
| H. Steuber
|
 | 2PDC | Human aldose reductase mutant F121P complexed with IDD393 | View ligand
| H. Steuber
|
 | 2PDB | Human aldose reductase mutant F121P complexed with zopolrestat | View ligand
| H. Steuber
|
 | 2PD9 | Human aldose reductase mutant V47I complexed with fidarestat | View ligand
| H. Steuber
|
 | 2PD5 | Human aldose reductase mutant V47I complexed with zopolrestat | View ligand
| H. Steuber
|
 | 3BIV | Human thrombin in complex with UB-THR11 | View ligand
| C. Gerlach
|
 | 3BIU | Human thrombin in complex with UB-THR10 | View ligand
| C. Gerlach
|
 | 2NSO | tRNA-guanine-transglycosylase (TGT) mutant Y106F, C158V, A232S, V233G- APO-Structure | | N. Tidten
|
 | 2NQZ | tRNA-guanine transglycosylase (TGT) mutant in complex with 7-deaza-7-aminomethyl-guanine | View ligand
| N. Tidten
|
 | 2Z1X | tRNA guanine transglycosylase E235Q mutant in complex with preQ1 | View ligand
| N. Tidten
|
 | 2Z1W | tRNA guanine transglycosylase TGT E235Q mutant in complex with BDI (2-Butyl-5,6-dihydro-1H-imidazo[4,5-D]pyridazine-4,7-dione) | View ligand
| N. Tidten
|
 | 2Z1V | tRNA guanine transglycosylase E235Q mutant apo structure, pH 8.5 | | N. Tidten
|
 | 2PWV | tRNA guanine transglycosylase E235Q mutant in complex with preQ0 | View ligand
| N. Tidten
|
 | 2PWU | tRNA guanine transglycosylase in complex with guanine | View ligand
| N. Tidten
|
 | 2POT | tRNA guanine transglycosylase (TGT) E235Q mutant in complex with guanine | View ligand
| N. Tidten
|
 | 2OKO | Z. mobilis tRNA guanine transglycosylase E235Q mutant apo-structure at pH 5.5 | | N. Tidten
|
 | 2Q38 | Carbonic Anhydrase II in complex with Saccharin at 1.95 Angstrom | View ligand
| J. Schulze-Wischeler
|
 | 2QZR | tRNA-Guanine Transglycosylase(TGT) in Complex with 6-amino-2-[(1-naphthylmethyl)amino]-3,7-dihydro-8H-imidazo[4,5-g]quinazolin-8-one | View ligand
| T. Ritschel
|
 | 2Q1B | Carbonic Anhydrase II in Complex with Saccharin | View ligand
| K. Koehler
|
 | 2QII | Crystal Structure of tRNA-Guanine Transglycosylase (TGT) From Zymomonas mobilis Complexed With Archaeosine Precursor, Preq0 | View ligand
| N. Tidten
|
 | 2IKJ | Human aldose reductase complexed with nitro-substituted IDD-type inhibitor | View ligand
| H. Steuber
|
 | 2IKI | Human aldose reductase complexed with halogenated IDD-type inhibitor | View ligand
| H. Steuber
|
 | 2IKH | Human aldose reductase complexed with nitrofuryl-oxadiazol inhibitor at 1.55 A | View ligand
| H. Steuber
|
 | 2IKG | Aldose reductase complexed with nitrophenyl-oxadiazol type inhibitor at 1.43 A | View ligand
| H. Steuber
|
 | 2NVD | Human Aldose Reductase complexed with novel naphtho[1,2-d]isothiazole acetic acid derivative (2) | View ligand
| H. Steuber
|
 | 2NVC | Human Aldose Reductase complexed with novel naphtho[1,2-d]isothiazole acetic acid derivative (3) | View ligand
| H. Steuber
|
 | 2BBF | Crystal structure of tRNA-guanine transglycosylase (TGT) from Zymomonas mobilis in complex with 6-amino-3,7-dihydro-imidazo[4,5-g]quinazolin-8-one | View ligand
| B. Stengl
|
 | 2HVO | Human Aldose Reductase-zopolrestat complex obtained by cocrystallisation (10days_cocryst) | View ligand
| H. Steuber
|
 | 2HVN | Human Aldose Reductase-zopolrestat complex obtained by cocrystallisation after one day (1day_cocryst) | View ligand
| H. Steuber
|
 | 2HV5 | Human Aldose Reductase complexed with inhibitor zopolrestat after three days soaking (3days_soaked_3) | View ligand
| H. Steuber
|
 | 2FZD | Human aldose reductase complexed with tolrestat at 1.08 A resolution | View ligand
| H. Steuber
|
 | 2FZB | Human Aldose Reductase complexed with four tolrestat molecules at 1.5 A resolution. | View ligand
| H. Steuber
|
 | 2FZ9 | Human Aldose Reductase complexed with inhibitor zopolrestat after six days soaking. | View ligand
| H. Steuber
|
 | 2FZ8 | Human Aldose reductase complexed with inhibitor zopolrestat at 1.48 A(1 day soaking). | View ligand
| H. Steuber
|
 | 2DV0 | Human Aldose Reductase complexed with zopolrestat after 6 days soaking(6days_soaked_2) | View ligand
| H. Steuber
|
 | 2DUZ | Human Aldose Reductase complexed with inhibitor zopolrestat after 3 days soaking (3days_soaked_2) | View ligand
| H. Steuber
|
 | 2DUX | Crystal structure of human Aldose Reductase complexed with zopolrestat after 3 days soaking (3days_soaked_1) | View ligand
| H. Steuber
|
 | 1ZH9 | Carbonic anhydrase II in complex with N-4-Methyl-1-piperazinyl-N'-(p-sulfonamide)phenylthiourea as sulfonamide inhibitor | View ligand
| V. Honndorf
|
 | 1ZGF | Carbonic anhydrase II in complex with trichloromethiazide as sulfonamide inhibitor | View ligand
| V. Honndorf
|
 | 1ZGE | Carbonic anhydrase II in complex with p-Sulfonamido-o,o'-dichloroaniline as sulfonamide inhibitor | View ligand
| V. Honndorf
|
 | 1ZFQ | Carbonic anhydrase II in complex with ethoxzolamidphenole as sulfonamide inhibitor | View ligand
| V. Honndorf
|
 | 1ZFK | Carbonic anhydrase II in complex with N-4-sulfonamidphenyl-N'-4-methylbenzosulfonylurease as sulfonamide inhibitor | View ligand
| V. Honndorf
|
 | 1Z9Y | Carbonic anhydrase II in complex with furosemide as sulfonamide inhibitor | View ligand
| V. Honndorf
|
 | 1YY3 | Structure of S-Adenosylmethionine:tRNA Ribosyltransferase-Isomerase (QueA) | | C. Grimm
|
 | 1Z8A | Human Aldose Reductase complexed with novel Sulfonyl-pyridazinone Inhibitor | View ligand
| H. Steuber
|
 | 1Z89 | Human Aldose Reductase complexed with novel Sulfonyl-pyridazinone Inhibitor | View ligand
| H. Steuber
|
 | 1YPK | Thrombin Inhibitor Complex | View ligand
| J. Fokkens
|
 | 1YPJ | Thrombin Inhibitor Complex | View ligand
| J. Fokkens
|
 | 1YPG | Thrombin Inhibitor Complex | View ligand
| J. Fokkens
|
 | 1YPE | Thrombin Inhibitor Complex | View ligand
| J. Fokkens
|
 | 1YP9 | Trypsin Inhibitor Complex | View ligand
| J. Fokkens
|
 | 1Y5X | tRNA-guanine Transglycosylase (TGT) in complex with 6-Amino-4-[2-(4-methoxyphenyl)ethyl]-1,7-dihydro-8H-imidazo[4,5-g]quinazolin-8-one | View ligand
| B. Stengl
|
 | 1Y5W | tRNA-guanine Transglycosylase (TGT) in complex with 6-Amino-4-[2-(4-methylphenyl)ethyl]-1,7-dihydro-8H-imidazo[4,5-g]quinazolin-8-one | View ligand
| B. Stengl
|
 | 1Y5V | tRNA-Guanine Transglycosylase (TGT) in complex with 6-Amino-4-(2-phenylethyl)-1,7-dihydro-8H-imidazo[4,5-g]quinazolin-8-one | View ligand
| B. Stengl
|
 | 1Y5U | Dianhydrosugar-based benzamidine, factor Xa specific inhibitor in complex with bovine trypsin mutant | View ligand
| A. DiFenza
|
 | 1Y5B | Dianhydrosugar-based benzamidine, factor Xa specific inhibitor in complex with bovine trypsin mutant | View ligand
| A. DiFenza
|
 | 1Y5A | Dianhydrosugar-based benzamidine, factor Xa specific inhibitor in complex with bovine trypsin mutant | View ligand
| A. DiFenza
|
 | 1Y59 | Dianhydrosugar-based benzamidine, factor Xa specific inhibitor in complex with bovine trypsin mutant | View ligand
| A. DiFenza
|
 | 1Y3Y | Trypsin Inhibitor Complex | View ligand
| J. Fokkens
|
 | 1Y3X | Trypsin Inhibitor Complex | View ligand
| J. Fokkens
|
 | 1Y3W | Trypsin Inhibitor Complex | View ligand
| J. Fokkens
|
 | 1Y3V | Trypsin Inhibitor Complex | View ligand
| J. Fokkens
|
 | 1Y3U | Trypsin Inhibitor Complex | View ligand
| J. Fokkens
|
 | 2AGT | Aldose Reductase Mutant Leu 300 Pro complexed with Fidarestat | View ligand
| H. Steuber
|
 | 1YVM | E. coli Methionine Aminopeptidase in complex with thiabendazole | View ligand
| R. Schiffmann
|
 | 1XL5 | HIV-1 Protease in complex with amidhyroxysulfone | View ligand
| J. Boettcher
|
 | 1XL2 | HIV-1 Protease in complex with pyrrolidinmethanamine | View ligand
| J. Boettcher
|
 | 2BMA | The Crystal Structure of Plasmodium Falciparum Glutamate Dehydrogenase, a Putative Target for Novel Antimalarial Drugs | | C. Werner
|
 | 1S39 | Crystal Structure of TGT in Complex with 2-aminoquinazolin-4(3H)-one | View ligand
| R. Brenk
|
 | 1SNY | Carbonyl reductase Sniffer of D. melanogaster | | T. Sgraja
|
 | 1S38 | Crystal Structure of TGT in Complex with 2-Amino-8-Methylquinazolin-4(3H)-one | View ligand
| R. Brenk
|
 | 1V2W | Trypsin inhibitor in complex with bovine trypsin variant X(SSAI)bT.B4 | View ligand
| D. Rauh
|
 | 1V2V | Benzamidine in complex with bovine trypsin variant X(SSAI)bT.C1 | View ligand
| D. Rauh
|
 | 1V2U | Benzamidine in complex with bovine trypsin varinat X(SSAI)bT.D1 | View ligand
| D. Rauh
|
 | 1V2T | Trypsin inhibitor in complex with bovine trypsin variant X(SSFI.Glu)bT.B4 | View ligand
| D. Rauh
|
 | 1V2S | Benzamidine in complex with bovine trypsin variant X(SSFI.Glu)bT.D1 | View ligand
| D. Rauh
|
 | 1V2R | Trypsin inhibitor in complex with bovine trypsin variant X(SSRI)bT.B4 | View ligand
| D. Rauh
|
 | 1V2Q | Trypsin inhibitor in complex with bovine trypsin variant X(SSWI)bT.B4 | View ligand
| D. Rauh
|
 | 1V2P | Trypsin inhibitor in complex with bovine trypsin variant X(SSYI)bT.A4 | View ligand
| D. Rauh
|
 | 1V2O | Trypsin inhibitor in complex with bovine trypsin variant X(SSYI)bT.B4 | View ligand
| D. Rauh
|
 | 1V2N | Potent factor XA inhibitor in complex with bovine trypsin variant X(99/175/190)bT | View ligand
| D. Rauh
|
 | 1V2M | Benzamidine in complex with bovine trypsin variant X(triple.Glu)bT.A1 | View ligand
| D. Rauh
|
 | 1V2L | Benzamidine in complex with bovine trypsin variant X(triple.Glu)bT.D1 | View ligand
| D. Rauh
|
 | 1V2K | Factor XA specific Inhibitor in complex with bovine trypsin variant X(triple.Glu)bT.D2 | View ligand
| D. Rauh
|
 | 1V2J | Benzamidine in Complex with Bovine Trypsin Variant X(SSRI)bT.C1 | View ligand
| D. Rauh
|
 | 1R5Y | Crystal Structure of TGT in complex with 2,6-Diamino-3H-Quinazolin-4-one Crystallized at PH 5.5 | View ligand
| R. Brenk
|
 | 1Q66 | Crystal Structure of TGT in Complex with 2-Amino-6-aminomethyl-8-phenylsulfanylmethyl-3H-quinazolin-4-one crystallized at pH 5.5 | View ligand
| R. Brenk
|
 | 1Q65 | Crystal Structure of TGT in Complex with2,6-diamino-8-(2-dimethylaminoethylsulfanylmethyl)-3H-quinazolin-4-one crystallized at pH 5.5 | View ligand
| R. Brenk
|
 | 1Q63 | Crystal Structure of TGT in Complex with 2,6-Diamino-8-(1H-imidazol-2-ylsulfanylmethyl)-3H-quinazoline-4-one crystallized at pH 5.5 | View ligand
| R. Brenk
|
 | 1Q4W | Crystal Structure of TGT in Complex with 2,6-diamino-3H-quinazolin-4-one | View ligand
| R. Brenk
|
 | 1OQ5 | Carbonic Anhydrase II in Complex with Nanomolar Inhibitor | View ligand
| A. Weber
|
 | 1P0E | Crystal Structure of Zymomonas Mobilis tRNA-Guanine Transglycosylase (TGT) Cocrystallised with PreQ1 at pH 5.5 | View ligand
| R. Brenk
|
 | 1P0D | Crystal Structure of Zymomonas Mobilis tRNA-Guanine Transglycosylase (TGT) Crystallised at pH 5.5 | | R. Brenk
|
 | 1P0B | Crystal Structure of tRNA-Guanine Transglycosylase (TGT) From Zymomonas Mobilis Complexed With Archaeosine Precursor, Preq0 | View ligand
| R. Brenk
|
 | 1OZQ | Crystal Structure of the Mutated tRNA-Guanine Transglycosylase (TGT) Y106F Complexed with PreQ1 | View ligand
| R. Brenk
|
 | 1OZM | Y106F mutant of Z. mobilis TGT | | R. Brenk
|
 | 1PXG | Crystal structure of the mutated tRNA-guanine transglycosylase (TGT) D280E complexed with preQ1 | View ligand
| T. Sgraja
|
 | 1MUM | Structure of the 2-Methylisocitrate Lyase (PrpB) from Escherichia coli | | C. Grimm
|
 | 1N2V | Crystal Structure of TGT in complex with 2-Butyl-5,6-dihydro-1H-imidazo[4,5-d]pyridazine-4,7-dione | View ligand
| R. Brenk
|
 | 1KWR | Human Carbonic Anhydrase II complexed with Inhibitor 0134-36 | View ligand
| S. Grueneberg
|
 | 1KWQ | Human Carbonic Anhydrase II complexed with Inhibitor2000-07 | View ligand
| S. Grueneberg
|
 | 1J17 | Factor XA Specific Inhibitor in Complex with Rat Trypsin Mutant X99/175/190RT | View ligand
| M. Stubbs
|
 | 1J16 | Benzamidine in Complex with Rat Trypsin Mutant X99/175/190RT | View ligand
| M. Stubbs
|
 | 1J15 | Benzamidine in Complex with Rat Trypsin Mutant X99/175/190RT | View ligand
| M. Stubbs
|
 | 1J14 | Benzamidine in Complex with Rat Trypsin Mutant X99RT | View ligand
| M. Stubbs
|
 | 1K22 | Human Thrombin-Inhibitor Complex | View ligand
| M. Stubbs
|
 | 1K21 | Human Thrombin-Inhibitor Complex | View ligand
| M. Stubbs
|
 | 1K4H | Crystal Structure of tRNA-Guanine Transglycosylase (TGT) Complexed with 2,6-Diamino-8-propylsulfanylmethyl-3H-quinazoline-4-one | View ligand
| R. Brenk
|
 | 1K4G | Crystal Structure of tRNA-Guanine Transglycosylase (TGT) Complexed with 2,6-Diamino-8-(1H-imidazol-2-ylsulfanylmethyl)-3H-quinazoline-4-one | View ligand
| R. Brenk
|
 | 1K5H | 1-deoxy-D-xylulose-5-phosphate reductoisomerase | | K. Reuter
|
