Struktur Bibliothek der Arbeitsgruppe Prof. Dr. G. Klebe
Structures in gallery: 332
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2012 (43 structures)
| 3QP0 | HIV-1 protease (mutant Q7K L33I L63I) in complex with a novel inhibitor | Lindemann, Ina Dr. | ||
| 3QPJ | HIV-1 protease (mutant Q7K L33I L63I) in complex with a three-armed pyrrolidine-based inhibitor | Lindemann, Ina Dr. | ||
| 3QRM | HIV-1 protease (mutant Q7K L33I L63I) in complex with a three-armed pyrrolidine-based inhibitor | Lindemann, Ina Dr. | ||
| 3QRO | HIV-1 protease (mutant Q7K L33I L63I) in complex with a three-armed pyrrolidine-based inhibitor | Lindemann, Ina Dr. | ||
| 3QRS | HIV-1 protease (mutant Q7K L33I L63I) in complex with a three-armed pyrrolidine-based inhibitor | Lindemann, Ina Dr. | ||
| 3S3J | Transglutaminase 2 in complex with a novel inhibitor | Lindemann, Ina Dr. | ||
| 3S3P | Transglutaminase 2 in complex with a novel inhibitor | Lindemann, Ina Dr. | ||
| 3S3S | Transglutaminase 2 in complex with a novel inhibitor | Lindemann, Ina Dr. | ||
| 3QTO | Thrombin Inhibition by Pyridin Derivatives | Biela, Adam Dr. | ||
| 3QTV | Thrombin Inhibition by Pyridin Derivatives | Biela, Adam Dr. | ||
| 3QWC | Thrombin Inhibition by Pyridin Derivatives | Biela, Adam Dr. | ||
| 3QX5 | Thrombin Inhibition by Pyridin Derivatives | Biela, Adam Dr. | ||
| 3RLW | Human Thrombin in complex with MI328 | Biela, Adam Dr. | ||
| 3RLY | Human Thrombin in complex with MI329 | Biela, Adam Dr. | ||
| 3RM0 | Human Thrombin in complex with MI354 | Biela, Adam Dr. | ||
| 3RM2 | Human Thrombin in complex with MI003 | Biela, Adam Dr. | ||
| 3RML | Human Thrombin in complex with MI331 | Biela, Adam Dr. | ||
| 3RMM | Human Thrombin in complex with MI332 | Biela, Adam Dr. | ||
| 3RMN | Human Thrombin in complex with MI341 | Biela, Adam Dr. | ||
| 3RMO | Human Thrombin in complex with MI004 | Biela, Adam Dr. | ||
| 3SHA | Human Thrombin In Complex With UBTHR97 | Biela, Adam Dr. | ||
| 3SHC | Human Thrombin In Complex With UBTHR101 | Biela, Adam Dr. | ||
| 3SI3 | Human Thrombin In Complex With UBTHR103 | Biela, Adam Dr. | ||
| 3SI4 | Human Thrombin In Complex With UBTHR104 | Biela, Adam Dr. | ||
| 3SV2 | Human Thrombin In Complex With UBTHR105 | Biela, Adam Dr. | ||
| 3T5F | Human Thrombin In Complex With MI340 | Biela, Adam Dr. | ||
| 3T73 | Thermolysin In Complex With UBTLN22 | Biela, Adam Dr. | ||
| 3T74 | Thermolysin In Complex With UBTLN27 | Biela, Adam Dr. | ||
| 3T87 | Thermolysin In Complex With UBTLN28 | Biela, Adam Dr. | ||
| 3T8C | Thermolysin In Complex With UBTLN30 | Biela, Adam Dr. | ||
| 3T8D | Thermolysin In Complex With UBTLN31 | Biela, Adam Dr. | ||
| 3T8F | Thermolysin In Complex With UBTLN34 | Biela, Adam Dr. | ||
| 3T8G | Thermolysin In Complex With UBTLN26 | Biela, Adam Dr. | ||
| 3T8H | Thermolysin In Complex With UBTLN29 | Biela, Adam Dr. | ||
| 3Q6Y | Endothiapepsin in complex with a pyrrolidine based inhibitor | Köster, Helene Dr. | ||
| 3Q70 | Secreted aspartic protease in complex with ritonavir | Köster, Helene Dr. | ||
| 3T6I | Endothiapepsin in complex with an azepin derivative | Köster, Helene Dr. | ||
| 3T7P | Endothiapepsin in complex with a hydrazide derivative | Köster, Helene Dr. | ||
| 3T7Q | Endothiapepsin in complex with an inhibitor based on the Gewald reaction | Köster, Helene Dr. | ||
| 3T7X | Endothiapepsin in complex with an inhibitor based on the Gewald reaction | Köster, Helene Dr. | ||
| 3QBF | HIV-1 protease (mutant Q7K L33I L63I) in complex with a three-armed pyrrolidine-based inhibitor | Lindemann, Ina Dr. | ||
| 3QIH | HIV-1 protease (mutant Q7K L33I L63I) in complex with a novel inhibitor | Lindemann, Ina Dr. | ||
| 3QN8 | HIV-1 protease (mutant Q7K L33I L63I) in complex with a novel inhibitor | Lindemann, Ina Dr. |
2011 (54 structures)
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3NN7 | Crystal structure of Thermolysin in complex with 2-bromoacetate |
View ligand |
Behnen, Jürgen Dr. |
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3N9W | Crystal structure of 2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase (IspD) in complex with 1,2-Propanediol |
View ligand View ligand |
Behnen, Jürgen Dr. |
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3N4A | Crystal structure of D-Xylose Isomerase in complex with S-1,2-Propandiol |
View ligand |
Behnen, Jürgen Dr. |
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3N21 | Crystal structure of Thermolysin in complex with S-1,2-Propandiol |
View ligand |
Behnen, Jürgen Dr. |
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3LZY | Crystal structure of Endothiapesin in complex with Xenon |
View ligand |
Behnen, Jürgen Dr. |
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3MSN | Crystal structure of Thermolysin in complex with N-methylurea |
View ligand |
Behnen, Jürgen Dr. |
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3MSF | Crystal structure of Thermolysin in complex with Urea |
View ligand |
Behnen, Jürgen Dr. |
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3MSA | Crystal structure of Thermolysin in complex with 3-Bromophenol |
View ligand |
Behnen, Jürgen Dr. |
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3MS3 | Crystal structure of Thermolysin in complex with Aniline |
View ligand |
Behnen, Jürgen Dr. |
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3M3D | Crystal structure of Acetylcholinesterase in complex with Xenon |
View ligand |
Behnen, Jürgen Dr. |
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3LS7 | Crystal structure of Thermolysin in complex with Xenon |
View ligand |
Behnen, Jürgen Dr. |
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3M2Z | Fragment tethered to Carbonic Anhydrase II H64C mutant |
View ligand |
Schulze Wischeler, Johannes Dr. |
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3M5T | Fragment tethered to Carbonic Anhydrase II H64C mutant |
View ligand |
Schulze Wischeler, Johannes Dr. |
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3M5S | Carbonic Anhydrase II mutant H64C in complex with carbonate |
View ligand |
Schulze Wischeler, Johannes Dr. |
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3M2Y | Carbonic Anhydrase II in complex with novel sulfonamide inhibitor |
View ligand |
Schulze Wischeler, Johannes Dr. |
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3M2X | Carbonic Anhydrase II in complex with novel sulfonamide inhibitor |
View ligand |
Schulze Wischeler, Johannes Dr. |
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3M1W | Carbonic Anhyrdase II mutant W5CH64C with closed disulfide bond in complex with sulfate |
View ligand |
Schulze Wischeler, Johannes Dr. |
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3M1Q | Carbonic Anhydrase II mutant W5C-H64C with opened disulfide bond | Schulze Wischeler, Johannes Dr. | |
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3M14 | Carbonic Anhydrase II in complex with novel sulfonamide inhibitor |
View ligand |
Schulze Wischeler, Johannes Dr. |
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3M04 | Carbonic Anhydrase II in complex with novel sulfonamide inhibitor |
View ligand |
Schulze Wischeler, Johannes Dr. |
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3KNE | Carbonic Anhydrase II H64C mutant in complex with an in situ formed triazole |
View ligand |
Schulze Wischeler, Johannes Dr. |
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3P17 | Thrombin Inhibition by Pyridin Derivatives |
View ligand |
Biela, Adam Dr. |
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3P2V | Novel Benzothiazepine Inhibitor in Complex with human Aldose Reductase |
View ligand |
Koch, Cornelia Dr. |
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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 |
Koch, Cornelia Dr. |
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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 |
Koch, Cornelia Dr. |
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3MC5 | Human Aldose Reductase mutant T113V in complex with IDD393 crystallized in spacegroup P1 |
View ligand |
Koch, Cornelia Dr. |
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3MB9 | Human Aldose Reductase mutant T113A complexed with Zopolrestat |
View ligand |
Koch, Cornelia Dr. |
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3M64 | Human aldose reductase mutant T113V complexed with IDD393 |
View ligand |
Koch, Cornelia Dr. |
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3M0I | Human Aldose Reductase mutant T113V in complex with Zopolrestat |
View ligand |
Koch, Cornelia Dr. |
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3LEN | Human Aldose Reductase mutant T113S complexed with Zopolrestat |
View ligand |
Koch, Cornelia Dr. |
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3POO | Human cAMP-dependent protein kinase in complex with an inhibitor |
View ligand View ligand |
Köster, Helene Dr. |
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3PMY | Endothiapepsin in complex with a fragment |
View ligand |
Köster, Helene Dr. |
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3PMU | Endothiapepsin in complex with a fragment |
View ligand |
Köster, Helene Dr. |
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3PM4 | Endothiapepsin in complex with a fragment |
View ligand |
Köster, Helene Dr. |
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3PLL | Endothiapepsin in complex with a fragment |
View ligand |
Köster, Helene Dr. |
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3PLD | Endothiapepsin in complex with a fragment |
View ligand |
Köster, Helene Dr. |
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3PI0 | Endothiapepsin in complex with a fragment |
View ligand |
Köster, Helene Dr. |
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3PRS | Endothiapepsin in complex with ritonavir |
View ligand |
Köster, Helene Dr. |
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3PGI | Endothiapepsin in complex with a fragment |
View ligand |
Köster, Helene Dr. |
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3PCZ | Endothiapepsin in complex with benzamidine |
View ligand |
Köster, Helene Dr. |
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3PCW | Endothiapepsin in complex with a fragment |
View ligand |
Köster, Helene Dr. |
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3PBZ | Endothiapepsin in complex with a fragment |
View ligand |
Köster, Helene Dr. |
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3PBD | Endothiapepsin in complex with a fragment |
View ligand |
Köster, Helene Dr. |
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3PB5 | Endothiapepsin in complex with a fragment |
View ligand |
Köster, Helene Dr. |
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3P0M | Human cAMP-dependent protein kinase in complex with an inhibitor |
View ligand |
Köster, Helene Dr. |
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3OXT | Human cAMP-dependent protein kinase in complex with an inhibitor |
View ligand |
Köster, Helene Dr. |
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3OWP | Human cAMP-dependent protein kinase in complex with an inhibitor |
View ligand |
Köster, Helene Dr. |
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3OVV | Human cAMP-dependent protein kinase in complex with an inhibitor |
View ligand View ligand |
Köster, Helene Dr. |
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3OOG | Human cAMP-dependent protein kinase in complex with a small fragment |
View ligand |
Köster, Helene Dr. |
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3NX8 | Human cAMP dependent protein kinase in complex with phenol |
View ligand |
Köster, Helene Dr. |
| 3PSY | Endothiapepsin in complex with an inhibitor based on the Gewald reaction | Köster, Helene Dr. | ||
| 3PVK | Secreted aspartic protease 2 in complex with benzamidine | Köster, Helene Dr. | ||
| 3PWW | Endothiapepsin in complex with saquinavir | Köster, Helene Dr. | ||
| 3PSU | HIV-1 protease in complex with an isobutyl decorated oligoamine (symmetric binding mode) | Lindemann, Ina Dr. |
2010 (20 structures)
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3M1K | Carbonic Anhydrase in complex with fragment |
View ligand |
Schulze Wischeler, Johannes Dr. |
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3KIG | Mutant carbonic anhydrase II in complex with an azide and an alkyne |
View ligand View ligand |
Schulze Wischeler, Johannes Dr. |
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3FXS | Metal exchange in thermolysin |
View ligand |
Englert, Lisa Dr. |
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3FXP | Thermolysin inhibition |
View ligand |
Englert, Lisa Dr. |
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3FWD | Thermolysin inhibition |
View ligand |
Englert, Lisa Dr. |
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3FVP | Thermolysin inhibition |
View ligand |
Englert, Lisa Dr. |
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3FV4 | Thermolysin inhibition |
View ligand |
Englert, Lisa Dr. |
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3FLF | Thermolysin inhibition |
View ligand |
Englert, Lisa Dr. |
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3LJO | Bovine trypsin in complex with UB-THR 11 |
View ligand |
Wegscheid-Gerlach, Christof Dr. |
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3LJJ | Bovine trypsin in complex with UB-THR 10 |
View ligand |
Wegscheid-Gerlach, Christof Dr. |
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3M4H | Human Aldose Reductase mutant T113V complexed with IDD388 |
View ligand |
Koch, Cornelia Dr. |
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3LZ5 | Human aldose reductase mutant T113V complexed with IDD594 |
View ligand |
Koch, Cornelia Dr. |
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3LZ3 | Human aldose reductase mutant T113S complexed with IDD388 |
View ligand |
Koch, Cornelia Dr. |
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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 |
Ritschel, Tina Dr. |
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3LQL | Human Aldose Reductase mutant T113A complexed with IDD 594 |
View ligand |
Koch, Cornelia Dr. |
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3GEV | tRNA-guanine transglycosylase in complex with 2-[(2-Thienylmethyl)amino]-1,7-dihydro-8H-imidazo[4,5-g]quinazolin-8-one |
View ligand |
Ritschel, Tina Dr. |
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3LQG | Human aldose reductase mutant T113A complexed with IDD388 |
View ligand |
Koch, Cornelia Dr. |
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3LEP | Human Aldose Reductase mutant T113C in complex with IDD388 |
View ligand |
Koch, Cornelia Dr. |
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3LD5 | Human aldose reductase mutant T113S complexed with IDD594 |
View ligand |
Koch, Cornelia Dr. |
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3LBO | Human aldose reductase mutant T113C complexed with IDD594 |
View ligand |
Koch, Cornelia Dr. |
2009 (41 structures)
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3CKT | HIV-1 protease in complex with a dimethylallyl decorated pyrrolidine based inhibitor (orthorombic space group) |
View ligand |
Boettcher, Jark Dr. |
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2ZGA | HIV-1 protease in complex with a dimethylallyl decorated pyrrolidine based inhibitor (hexagonal space group) |
View ligand |
Boettcher, Jark Dr. |
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3FGD | Drugscore FP: Thermoylsin in complex with fragment. |
View ligand |
Englert, Lisa Dr. |
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3FBO | Metal exchange in Thermolysin | Englert, Lisa Dr. | |
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3FB0 | Metal exchange in thermolysin | Englert, Lisa Dr. | |
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3F2P | Thermolysin inhibition |
View ligand |
Englert, Lisa Dr. |
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3F28 | Thermolysin inhibition |
View ligand |
Englert, Lisa Dr. |
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3EIM | Metal exchange in Thermolysin | Englert, Lisa Dr. | |
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3F68 | Thrombin Inhibition |
View ligand |
Baum, Bernhard Dr. |
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3EQ0 | Thrombin Inhibitor |
View ligand |
Baum, Bernhard Dr. |
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3DUX | Understanding Thrombin Inhibition |
View ligand |
Baum, Bernhard Dr. |
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3DT0 | Understanding Thrombin Inhibition |
View ligand |
Baum, Bernhard Dr. |
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2ZQ2 | Exploring trypsin S3 pocket |
View ligand |
Brandt, Tobias |
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3DHK | Bisphenylic Thrombin Inhibitors |
View ligand |
Baum, Bernhard Dr. |
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2ZQ1 | Exploring trypsin S3 pocket |
View ligand |
Brandt, Tobias |
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3D49 | Thrombin Inhibition |
View ligand |
Baum, Bernhard Dr. |
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2ZHW | Exploring thrombin S3 pocket |
View ligand |
Brandt, Tobias |
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2ZO3 | Bisphenylic Thrombin Inhibitors |
View ligand |
Baum, Bernhard Dr. |
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2ZHF | Exploring thrombin S3 pocket |
View ligand |
Brandt, Tobias |
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2ZNK | Thrombin Inhibition |
View ligand |
Baum, Bernhard Dr. |
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2ZHE | Exploring thrombin S3 pocket |
View ligand |
Brandt, Tobias |
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2ZIQ | Thrombin Inhibition |
View ligand |
Baum, Bernhard Dr. |
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2ZHD | Exploring trypsin S3 pocket |
View ligand |
Brandt, Tobias |
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2ZI2 | Thrombin Inhibition |
View ligand |
Baum, Bernhard Dr. |
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2ZG0 | Exploring thrombin S3 pocket |
View ligand |
Brandt, Tobias |
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2ZHQ | Thrombin Inhibition |
View ligand |
Baum, Bernhard Dr. |
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2ZFT | Exploring trypsin S3 pocket |
View ligand |
Brandt, Tobias |
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2ZFS | Exploring trypsin S3 pocket |
View ligand |
Brandt, Tobias |
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2ZFR | Exploring thrombin S3 pocket |
View ligand |
Brandt, Tobias |
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2ZFQ | Exploring thrombin S3 pocket |
View ligand |
Brandt, Tobias |
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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 |
Ritschel, Tina Dr. |
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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 |
Ritschel, Tina Dr. |
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3GC4 | tRNA-guanine transglycosylase in complex with inhibitor |
View ligand |
Ritschel, Tina Dr. |
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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 |
Ritschel, Tina Dr. |
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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 |
Ritschel, Tina Dr. |
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3HFY | Mutant of tRNA-guanine transglycosylase (K52M) | Ritschel, Tina Dr. | |
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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 |
Ritschel, Tina Dr. |
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3C2Y | tRNA-Guanine Transglycosylase (TGT) in complex with 6-Amino-2-methyl-1,7-dihydro-imidazo[4,5-g]quinazolin-8-one |
View ligand |
Ritschel, Tina Dr. |
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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 |
Ritschel, Tina Dr. |
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3FCQ | Thermolysin inhibition |
View ligand |
Steuber, Holger Dr. |
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3DN5 | Aldose Reductase in complex with novel biarylic inhibitor |
View ligand |
Steuber, Holger Dr. |
2008 (54 structures)
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3BHE | HIV-1 protease in complex with a three armed pyrrolidine derivative |
View ligand |
Boettcher, Jark Dr. |
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2R43 | I50V HIV-1 protease in complex with an amino decorated pyrrolidine-based inhibitor |
View ligand |
Boettcher, Jark Dr. |
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3BGC | HIV-1 protease in complex with a benzyl decorated oligoamine |
View ligand |
Boettcher, Jark Dr. |
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3BGB | HIV-1 protease in complex with a isobutyl decorated oligoamine |
View ligand |
Boettcher, Jark Dr. |
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3BC4 | I84V HIV-1 protease in complex with a pyrrolidine diester |
View ligand |
Boettcher, Jark Dr. |
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2R3W | I84V HIV-1 protease in complex with a amino decorated pyrrolidine-based inhibitor |
View ligand |
Boettcher, Jark Dr. |
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2R3T | I50V HIV-1 protease mutant in complex with a carbamoyl decorated pyrrolidine-based inhibitor |
View ligand |
Boettcher, Jark Dr. |
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2R38 | I84V HIV-1 protease mutant in complex with a carbamoyl decorated pyrrolidine-based inhibitor |
View ligand |
Boettcher, Jark Dr. |
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2QNQ | HIV-1 Protease in complex with a chloro decorated pyrrolidine-based inhibitor |
View ligand |
Boettcher, Jark Dr. |
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2QNP | HIV-1 Protease in complex with a iodo decorated pyrrolidine-based inhibitor |
View ligand |
Boettcher, Jark Dr. |
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2QNN | HIV-1 protease in complex with a multiple decorated pyrrolidine-based inhibitor |
View ligand |
Boettcher, Jark Dr. |
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2PWR | HIV-1 protease in complex with a carbamoyl decorated pyrrolidine-based inhibitor |
View ligand |
Boettcher, Jark Dr. |
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2PWC | HIV-1 protease in complex with a amino decorated pyrrolidine-based inhibitor |
View ligand |
Boettcher, Jark Dr. |
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2PQZ | HIV-1 Protease in complex with a pyrrolidine-based inhibitor |
View ligand |
Boettcher, Jark Dr. |
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3BLO | TGT mutant in complex with queuine |
View ligand View ligand |
Tidten, Naomi Dr. |
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3BLL | TGT mutant in complex with Boc-preQ1 |
View ligand |
Tidten, Naomi Dr. |
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3BLD | tRNA guanine transglycosylase V233G mutant preQ1 complex structure |
View ligand |
Tidten, Naomi Dr. |
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3BL3 | tRNA guanine transglycosylase V233G mutant apo structure | Tidten, Naomi Dr. | |
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2ZGX | Thrombin Inhibition |
View ligand |
Baum, Bernhard Dr. |
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2ZGB | Thrombin Inhibition |
View ligand |
Baum, Bernhard Dr. |
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2ZFP | Thrombin Inibition |
View ligand |
Baum, Bernhard Dr. |
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2ZFF | Exploring Thrombin S1-pocket |
View ligand |
Baum, Bernhard Dr. |
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2ZF0 | Exploring Thrombin S1 Pocket |
View ligand |
Baum, Bernhard Dr. |
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2ZDV | Exploring Thrombin S1 pocket |
View ligand |
Baum, Bernhard Dr. |
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2ZDA | Exploring Thrombin S1 pocket |
View ligand |
Baum, Bernhard Dr. |
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2ZC9 | Thrombin in complex with Inhibitor |
View ligand |
Baum, Bernhard Dr. |
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3EGK | KNOBLE Inhibitor |
View ligand |
Baum, Bernhard Dr. |
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2ZDN | Exploring trypsin S3 pocket |
View ligand |
Brandt, Tobias |
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2ZDM | Exploring trypsin S3 pocket |
View ligand |
Brandt, Tobias |
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2ZDL | Exploring Trypsin S3 pocket |
View ligand |
Brandt, Tobias |
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2ZDK | Exploring Trypsin S3 Pocket |
View ligand |
Brandt, Tobias |
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2Z7K | tRNA-Guanine transglycosylase (TGT) in complex with 2-Amino-lin-Benzoguanine |
View ligand |
Ritschel, Tina Dr. |
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3BAZ | Structure of hydroxyphenylpyruvate reductase from coleus blumei in complex with NADP+ |
View ligand |
|
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3BA1 | Structure of hydroxyphenylpyruvate reductase from coleus blumei | ||
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2QAE | Crystal Structure Analysis of Trypanosoma cruzi Lipoamide dehydrogenase |
View ligand |
Werner, Christof Dr. |
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2PDY | Human aldose reductase double mutant S302R-C303D complexed with fidarestat |
View ligand |
Steuber, Holger Dr. |
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2PDX | Human aldose reductase double mutant S302R-C303D complexed with zopolrestat |
View ligand |
Steuber, Holger Dr. |
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2PDW | Human aldose reductase mutant C303D complexed with fidarestat |
View ligand |
Steuber, Holger Dr. |
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2PDU | Human aldose reductase mutant C303D complexed with IDD393 |
View ligand |
Steuber, Holger Dr. |
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2PDQ | Human aldose reductase mutant C303D complexed with uracil-type inhibitor |
View ligand |
Steuber, Holger Dr. |
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2PDP | Human aldose reductase mutant S302R complexed with IDD 393 |
View ligand |
Steuber, Holger Dr. |
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2PDN | Human aldose reductase mutant S302R complexed with uracil-type inhibitor |
View ligand |
Steuber, Holger Dr. |
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2PDM | Human aldose reductase mutant S302R complexed with zopolrestat |
View ligand |
Steuber, Holger Dr. |
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2PDL | Human aldose reductase mutant L301M complexed with tolrestat |
View ligand |
Steuber, Holger Dr. |
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2PDK | Human aldose reductase mutant L301M complexed with sorbinil |
View ligand |
Steuber, Holger Dr. |
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2PDJ | Human aldose reductase mutant L300A complexed with IDD393 |
View ligand |
Steuber, Holger Dr. |
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2PDI | Human aldose reductase mutant L300A complexed with zopolrestat at 1.55 A |
View ligand |
Steuber, Holger Dr. |
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2PDH | Human aldose reductase mutant L300P complexed with uracil-type inhibitor at 1.45 A |
View ligand |
Steuber, Holger Dr. |
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2PDG | Human aldose reductase with uracil-type inhibitor at 1.42A |
View ligand |
Steuber, Holger Dr. |
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2PDF | Human aldose reductase mutant L300P complexed with zopolrestat |
View ligand |
Steuber, Holger Dr. |
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2PDC | Human aldose reductase mutant F121P complexed with IDD393 |
View ligand |
Steuber, Holger Dr. |
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2PDB | Human aldose reductase mutant F121P complexed with zopolrestat |
View ligand |
Steuber, Holger Dr. |
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2PD9 | Human aldose reductase mutant V47I complexed with fidarestat |
View ligand |
Steuber, Holger Dr. |
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2PD5 | Human aldose reductase mutant V47I complexed with zopolrestat |
View ligand |
Steuber, Holger Dr. |
2007 (22 structures)
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2Q38 | Carbonic Anhydrase II in complex with Saccharin at 1.95 Angstrom |
View ligand |
Schulze Wischeler, Johannes Dr. |
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2Q1B | Carbonic Anhydrase II in Complex with Saccharin |
View ligand |
Köhler, Karen |
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2NSO | tRNA-guanine-transglycosylase (TGT) mutant Y106F, C158V, A232S, V233G- APO-Structure | Tidten, Naomi Dr. | |
![]() |
2NQZ | tRNA-guanine transglycosylase (TGT) mutant in complex with 7-deaza-7-aminomethyl-guanine |
View ligand |
Tidten, Naomi Dr. |
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2Z1X | tRNA guanine transglycosylase E235Q mutant in complex with preQ1 |
View ligand |
Tidten, Naomi Dr. |
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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 |
Tidten, Naomi Dr. |
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2Z1V | tRNA guanine transglycosylase E235Q mutant apo structure, pH 8.5 | Tidten, Naomi Dr. | |
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2PWV | tRNA guanine transglycosylase E235Q mutant in complex with preQ0 |
View ligand |
Tidten, Naomi Dr. |
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2PWU | tRNA guanine transglycosylase in complex with guanine |
View ligand |
Tidten, Naomi Dr. |
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2POT | tRNA guanine transglycosylase (TGT) E235Q mutant in complex with guanine |
View ligand |
Tidten, Naomi Dr. |
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2OKO | Z. mobilis tRNA guanine transglycosylase E235Q mutant apo-structure at pH 5.5 | Tidten, Naomi Dr. | |
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2QII | Crystal Structure of tRNA-Guanine Transglycosylase (TGT) From Zymomonas mobilis Complexed With Archaeosine Precursor, Preq0 |
View ligand |
Tidten, Naomi Dr. |
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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 |
Stengl, Bernhard Dr. |
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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 |
Ritschel, Tina Dr. |
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3BIV | Human thrombin in complex with UB-THR11 |
View ligand |
Wegscheid-Gerlach, Christof Dr. |
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3BIU | Human thrombin in complex with UB-THR10 |
View ligand |
Wegscheid-Gerlach, Christof Dr. |
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2IKJ | Human aldose reductase complexed with nitro-substituted IDD-type inhibitor |
View ligand |
Steuber, Holger Dr. |
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2IKI | Human aldose reductase complexed with halogenated IDD-type inhibitor |
View ligand |
Steuber, Holger Dr. |
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2IKH | Human aldose reductase complexed with nitrofuryl-oxadiazol inhibitor at 1.55 A |
View ligand |
Steuber, Holger Dr. |
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2IKG | Aldose reductase complexed with nitrophenyl-oxadiazol type inhibitor at 1.43 A |
View ligand |
Steuber, Holger Dr. |
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2NVD | Human Aldose Reductase complexed with novel naphtho[1,2-d]isothiazole acetic acid derivative (2) |
View ligand |
Steuber, Holger Dr. |
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2NVC | Human Aldose Reductase complexed with novel naphtho[1,2-d]isothiazole acetic acid derivative (3) |
View ligand |
Steuber, Holger Dr. |
2006 (24 structures)
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1YPK | Thrombin Inhibitor Complex |
View ligand |
Fokkens, Jasmine Dr. |
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1YPJ | Thrombin Inhibitor Complex |
View ligand |
Fokkens, Jasmine Dr. |
![]() |
1YPG | Thrombin Inhibitor Complex |
View ligand |
Fokkens, Jasmine Dr. |
![]() |
1YPE | Thrombin Inhibitor Complex |
View ligand |
Fokkens, Jasmine Dr. |
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1YP9 | Trypsin Inhibitor Complex |
View ligand |
Fokkens, Jasmine Dr. |
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1YY3 | Structure of S-Adenosylmethionine:tRNA Ribosyltransferase-Isomerase (QueA) | Grimm, Clemens Dr. | |
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1ZH9 | Carbonic anhydrase II in complex with N-4-Methyl-1-piperazinyl-N'-(p-sulfonamide)phenylthiourea as sulfonamide inhibitor |
View ligand |
Honndorf, Valerie |
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1ZGF | Carbonic anhydrase II in complex with trichloromethiazide as sulfonamide inhibitor |
View ligand |
Honndorf, Valerie |
![]() |
1ZGE | Carbonic anhydrase II in complex with p-Sulfonamido-o,o'-dichloroaniline as sulfonamide inhibitor |
View ligand |
Honndorf, Valerie |
![]() |
1ZFQ | Carbonic anhydrase II in complex with ethoxzolamidphenole as sulfonamide inhibitor |
View ligand |
Honndorf, Valerie |
![]() |
1ZFK | Carbonic anhydrase II in complex with N-4-sulfonamidphenyl-N'-4-methylbenzosulfonylurease as sulfonamide inhibitor |
View ligand |
Honndorf, Valerie |
![]() |
1Z9Y | Carbonic anhydrase II in complex with furosemide as sulfonamide inhibitor |
View ligand |
Honndorf, Valerie |
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2HVO | Human Aldose Reductase-zopolrestat complex obtained by cocrystallisation (10days_cocryst) |
View ligand |
Steuber, Holger Dr. |
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2HVN | Human Aldose Reductase-zopolrestat complex obtained by cocrystallisation after one day (1day_cocryst) |
View ligand |
Steuber, Holger Dr. |
![]() |
2HV5 | Human Aldose Reductase complexed with inhibitor zopolrestat after three days soaking (3days_soaked_3) |
View ligand |
Steuber, Holger Dr. |
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2FZD | Human aldose reductase complexed with tolrestat at 1.08 A resolution |
View ligand |
Steuber, Holger Dr. |
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2FZB | Human Aldose Reductase complexed with four tolrestat molecules at 1.5 A resolution. |
View ligand |
Steuber, Holger Dr. |
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2FZ9 | Human Aldose Reductase complexed with inhibitor zopolrestat after six days soaking. |
View ligand |
Steuber, Holger Dr. |
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2FZ8 | Human Aldose reductase complexed with inhibitor zopolrestat at 1.48 A(1 day soaking). |
View ligand |
Steuber, Holger Dr. |
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2DV0 | Human Aldose Reductase complexed with zopolrestat after 6 days soaking(6days_soaked_2) |
View ligand |
Steuber, Holger Dr. |
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2DUZ | Human Aldose Reductase complexed with inhibitor zopolrestat after 3 days soaking (3days_soaked_2) |
View ligand |
Steuber, Holger Dr. |
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2DUX | Crystal structure of human Aldose Reductase complexed with zopolrestat after 3 days soaking (3days_soaked_1) |
View ligand |
Steuber, Holger Dr. |
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1Z8A | Human Aldose Reductase complexed with novel Sulfonyl-pyridazinone Inhibitor |
View ligand |
Steuber, Holger Dr. |
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1Z89 | Human Aldose Reductase complexed with novel Sulfonyl-pyridazinone Inhibitor |
View ligand |
Steuber, Holger Dr. |
2005 (17 structures)
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1XL5 | HIV-1 Protease in complex with amidhyroxysulfone |
View ligand |
Boettcher, Jark Dr. |
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1XL2 | HIV-1 Protease in complex with pyrrolidinmethanamine |
View ligand |
Boettcher, Jark Dr. |
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1Y3Y | Trypsin Inhibitor Complex |
View ligand |
Fokkens, Jasmine Dr. |
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1Y3X | Trypsin Inhibitor Complex |
View ligand |
Fokkens, Jasmine Dr. |
![]() |
1Y3W | Trypsin Inhibitor Complex |
View ligand |
Fokkens, Jasmine Dr. |
![]() |
1Y3V | Trypsin Inhibitor Complex |
View ligand |
Fokkens, Jasmine Dr. |
![]() |
1Y3U | Trypsin Inhibitor Complex |
View ligand |
Fokkens, Jasmine Dr. |
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1Y5U | Dianhydrosugar-based benzamidine, factor Xa specific inhibitor in complex with bovine trypsin mutant |
View ligand |
Di Fenza, Armida Dr. |
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1Y5B | Dianhydrosugar-based benzamidine, factor Xa specific inhibitor in complex with bovine trypsin mutant |
View ligand |
Di Fenza, Armida Dr. |
![]() |
1Y5A | Dianhydrosugar-based benzamidine, factor Xa specific inhibitor in complex with bovine trypsin mutant |
View ligand |
Di Fenza, Armida Dr. |
![]() |
1Y59 | Dianhydrosugar-based benzamidine, factor Xa specific inhibitor in complex with bovine trypsin mutant |
View ligand |
Di Fenza, Armida Dr. |
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1YVM | E. coli Methionine Aminopeptidase in complex with thiabendazole |
View ligand |
|
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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 |
Stengl, Bernhard Dr. |
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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 |
Stengl, Bernhard Dr. |
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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 |
Stengl, Bernhard Dr. |
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2BMA | The Crystal Structure of Plasmodium Falciparum Glutamate Dehydrogenase, a Putative Target for Novel Antimalarial Drugs | Werner, Christof Dr. | |
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2AGT | Aldose Reductase Mutant Leu 300 Pro complexed with Fidarestat |
View ligand |
Steuber, Holger Dr. |
2004 (23 structures)
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1S39 | Crystal Structure of TGT in Complex with 2-aminoquinazolin-4(3H)-one |
View ligand |
Brenk, Ruth Dr. |
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1S38 | Crystal Structure of TGT in Complex with 2-Amino-8-Methylquinazolin-4(3H)-one |
View ligand |
Brenk, Ruth Dr. |
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1OQ5 | Carbonic Anhydrase II in Complex with Nanomolar Inhibitor |
View ligand |
Weber, Alexander Dr. |
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1R5Y | Crystal Structure of TGT in complex with 2,6-Diamino-3H-Quinazolin-4-one Crystallized at PH 5.5 |
View ligand |
Brenk, Ruth Dr. |
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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 |
Brenk, Ruth Dr. |
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1Q65 | Crystal Structure of TGT in Complex with2,6-diamino-8-(2-dimethylaminoethylsulfanylmethyl)-3H-quinazolin-4-one crystallized at pH 5.5 |
View ligand |
Brenk, Ruth Dr. |
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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 |
Brenk, Ruth Dr. |
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1Q4W | Crystal Structure of TGT in Complex with 2,6-diamino-3H-quinazolin-4-one |
View ligand |
Brenk, Ruth Dr. |
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1SNY | Carbonyl reductase Sniffer of D. melanogaster | Sgraja, Tanja Dr. | |
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1V2W | Trypsin inhibitor in complex with bovine trypsin variant X(SSAI)bT.B4 |
View ligand |
Rauh, Daniel Dr. |
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1V2V | Benzamidine in complex with bovine trypsin variant X(SSAI)bT.C1 |
View ligand |
Rauh, Daniel Dr. |
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1V2U | Benzamidine in complex with bovine trypsin varinat X(SSAI)bT.D1 |
View ligand |
Rauh, Daniel Dr. |
![]() |
1V2T | Trypsin inhibitor in complex with bovine trypsin variant X(SSFI.Glu)bT.B4 |
View ligand |
Rauh, Daniel Dr. |
![]() |
1V2S | Benzamidine in complex with bovine trypsin variant X(SSFI.Glu)bT.D1 |
View ligand |
Rauh, Daniel Dr. |
![]() |
1V2R | Trypsin inhibitor in complex with bovine trypsin variant X(SSRI)bT.B4 |
View ligand |
Rauh, Daniel Dr. |
![]() |
1V2Q | Trypsin inhibitor in complex with bovine trypsin variant X(SSWI)bT.B4 |
View ligand |
Rauh, Daniel Dr. |
![]() |
1V2P | Trypsin inhibitor in complex with bovine trypsin variant X(SSYI)bT.A4 |
View ligand |
Rauh, Daniel Dr. |
![]() |
1V2O | Trypsin inhibitor in complex with bovine trypsin variant X(SSYI)bT.B4 |
View ligand |
Rauh, Daniel Dr. |
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1V2N | Potent factor XA inhibitor in complex with bovine trypsin variant X(99/175/190)bT |
View ligand |
Rauh, Daniel Dr. |
![]() |
1V2M | Benzamidine in complex with bovine trypsin variant X(triple.Glu)bT.A1 |
View ligand |
Rauh, Daniel Dr. |
![]() |
1V2L | Benzamidine in complex with bovine trypsin variant X(triple.Glu)bT.D1 |
View ligand |
Rauh, Daniel Dr. |
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1V2K | Factor XA specific Inhibitor in complex with bovine trypsin variant X(triple.Glu)bT.D2 |
View ligand |
Rauh, Daniel Dr. |
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1V2J | Benzamidine in Complex with Bovine Trypsin Variant X(SSRI)bT.C1 |
View ligand |
Rauh, Daniel Dr. |
2003 (10 structures)
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1P0E | Crystal Structure of Zymomonas Mobilis tRNA-Guanine Transglycosylase (TGT) Cocrystallised with PreQ1 at pH 5.5 |
View ligand |
Brenk, Ruth Dr. |
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1P0D | Crystal Structure of Zymomonas Mobilis tRNA-Guanine Transglycosylase (TGT) Crystallised at pH 5.5 | Brenk, Ruth Dr. | |
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1P0B | Crystal Structure of tRNA-Guanine Transglycosylase (TGT) From Zymomonas Mobilis Complexed With Archaeosine Precursor, Preq0 |
View ligand |
Brenk, Ruth Dr. |
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1OZQ | Crystal Structure of the Mutated tRNA-Guanine Transglycosylase (TGT) Y106F Complexed with PreQ1 |
View ligand |
Brenk, Ruth Dr. |
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1OZM | Y106F mutant of Z. mobilis TGT | Brenk, Ruth Dr. | |
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1N2V | Crystal Structure of TGT in complex with 2-Butyl-5,6-dihydro-1H-imidazo[4,5-d]pyridazine-4,7-dione |
View ligand |
Brenk, Ruth Dr. |
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1KWR | Human Carbonic Anhydrase II complexed with Inhibitor 0134-36 |
View ligand |
Grüneberg, Sven Dr. |
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1KWQ | Human Carbonic Anhydrase II complexed with Inhibitor2000-07 |
View ligand |
Grüneberg, Sven Dr. |
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1MUM | Structure of the 2-Methylisocitrate Lyase (PrpB) from Escherichia coli | Grimm, Clemens Dr. | |
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1PXG | Crystal structure of the mutated tRNA-guanine transglycosylase (TGT) D280E complexed with preQ1 |
View ligand |
Sgraja, Tanja Dr. |
2002 (9 structures)
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1K5H | 1-deoxy-D-xylulose-5-phosphate reductoisomerase | Reuter, Klaus Prof. Dr. | |
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1J17 | Factor XA Specific Inhibitor in Complex with Rat Trypsin Mutant X99/175/190RT |
View ligand |
Stubbs, Milton Prof. Dr. |
![]() |
1J16 | Benzamidine in Complex with Rat Trypsin Mutant X99/175/190RT |
View ligand |
Stubbs, Milton Prof. Dr. |
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1J15 | Benzamidine in Complex with Rat Trypsin Mutant X99/175/190RT |
View ligand |
Stubbs, Milton Prof. Dr. |
![]() |
1J14 | Benzamidine in Complex with Rat Trypsin Mutant X99RT |
View ligand |
Stubbs, Milton Prof. Dr. |
![]() |
1K22 | Human Thrombin-Inhibitor Complex |
View ligand |
Stubbs, Milton Prof. Dr. |
![]() |
1K21 | Human Thrombin-Inhibitor Complex |
View ligand |
Stubbs, Milton Prof. Dr. |
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1K4H | Crystal Structure of tRNA-Guanine Transglycosylase (TGT) Complexed with 2,6-Diamino-8-propylsulfanylmethyl-3H-quinazoline-4-one |
View ligand |
Brenk, Ruth Dr. |
![]() |
1K4G | Crystal Structure of tRNA-Guanine Transglycosylase (TGT) Complexed with 2,6-Diamino-8-(1H-imidazol-2-ylsulfanylmethyl)-3H-quinazoline-4-one |
View ligand |
Brenk, Ruth Dr. |
2001 (9 structures)
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1K1P | Bovine Trypsin-Inhibitor Complex |
View ligand |
Stubbs, Milton Prof. Dr. |
![]() |
1K1O | Bovine Trypsin-Inhibitor Complex |
View ligand |
Stubbs, Milton Prof. Dr. |
![]() |
1K1N | Bovine Trypsin-Inhibitor Complex |
View ligand |
Stubbs, Milton Prof. Dr. |
![]() |
1K1M | Bovine Trypsin-Inhibitor Complex |
View ligand |
Stubbs, Milton Prof. Dr. |
![]() |
1K1L | Bovine Trypsin-Inhibitor Complex |
View ligand |
Stubbs, Milton Prof. Dr. |
![]() |
1K1J | Bovine Trypsin-Inhibitor Complex |
View ligand |
Stubbs, Milton Prof. Dr. |
![]() |
1K1I | Bovine Trypsin-Inhibitor Complex |
View ligand |
Stubbs, Milton Prof. Dr. |
![]() |
1FK8 | The Crystal Structure of the Binary Complex with NAD of 3-Alpha-Hydroxysteroid Dehydrogenase from Comamonas Testosteroni, a Member of the Short Chain Dehydrogenase/Reductase Family |
View ligand |
Grimm, Clemens Dr. |
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1FJH | The Crystal Structure of 3-Alpha-Hydroxysteroid Dehydrogenase from Comamonas Testosteroni, a Member of the Short Chain Dehydrogenase/Reductase Family | Grimm, Clemens Dr. |
2000 (6 structures)
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1QL9 | Factor XA Specific Inhibitor in Complex with Rat Trypsin Mutant X99RT |
View ligand |
Stubbs, Milton Prof. Dr. |
![]() |
1QL8 | Factor XA Specific Inhibitor in Complex with Bovine Trypsin |
View ligand |
Stubbs, Milton Prof. Dr. |
![]() |
1QL7 | Factor XA Specific Inhibitor in Complex with Bovine Trypsin |
View ligand |
Stubbs, Milton Prof. Dr. |
![]() |
1F3E | A New Target for Shigellosis: Rational Design and Crystallographic Studies of Inhibitors of tRNA-Guanine Transglycosylase |
View ligand |
Grädler, Ulrich Dr. |
![]() |
1ENU | A new target for shigellosis: Rational design and crystallographic studies of inhibitors of tRNA-guanine transglycosylase |
View ligand |
Grädler, Ulrich Dr. |
![]() |
1EFZ | Mutagenesis and Crystallographic Studies of Zymomonas Mobilis tRNA-Guanine Transglycosylase to Elucidate the Role of Serine 103 for Enzymatic Activity |
View ligand |
Grädler, Ulrich Dr. |
© Andreas Heine, Department of Pharmaceutical Chemistry, Marburg University.
This site was designed and is maintained by Andreas Heine (heinea@mailer.uni-marburg.de) and Timo Krotzky (krotzky@uni-marburg.de)
This site was designed and is maintained by Andreas Heine (heinea@mailer.uni-marburg.de) and Timo Krotzky (krotzky@uni-marburg.de)




























































































































































































































































































