Search Count: 16
 |
Structure Of P. Aeruginosa Lpxc With Compound 8: (2Rs)-4-(5-(2-Fluoro-4-Methoxyphenyl)-2-Oxooxazol-3(2H)-Yl)-N-Hydroxy-2-Methyl-2-(Methylsulfonyl)Butanamide
Organism: Pseudomonas aeruginosa lesb58
Method: X-RAY DIFFRACTION Resolution:1.75 Å Release Date: 2019-12-18 Classification: HYDROLASE Ligands: ZN, H2N, GOL |
Organism: Pseudomonas aeruginosa lesb58
Method: X-RAY DIFFRACTION
Release Date: 2019-12-18
Ligands: ZN, H2N, GOL
 |
Structure Of P. Aeruginosa Lpxc With Compound 10: (2Rs)-4-(5-(2-Fluoro-4-Methoxyphenyl)-1-Oxoisoindolin-2-Yl)-N-Hydroxy-2-Methyl-2-(Methylsulfonyl)Butanamide
Organism: Pseudomonas aeruginosa (strain lesb58)
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2019-12-18 Classification: HYDROLASE Ligands: ZN, UNY, UNZ |
Organism: Pseudomonas aeruginosa (strain lesb58)
Method: X-RAY DIFFRACTION
Release Date: 2019-12-18
Ligands: ZN, UNY, UNZ
 |
Structure Of P. Aeruginosa Lpxc With Compound 12: (2R)-4-(6-(2-Fluoro-4-Methoxyphenyl)-3-Oxo-1H-Pyrrolo[1,2-C]Imidazol-2(3H)-Yl)-N-Hydroxy-2-Methyl-2-(Methylsulfonyl)Butanamide
Organism: Pseudomonas aeruginosa lesb58
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2019-12-18 Classification: HYDROLASE Ligands: ZN, H2H, EDO |
Organism: Pseudomonas aeruginosa lesb58
Method: X-RAY DIFFRACTION
Release Date: 2019-12-18
Ligands: ZN, H2H, EDO
 |
Structure Of P. Aeruginosa Lpxc With Compound 17A: (2R)-N-Hydroxy-2-Methyl-2-(Methylsulfonyl)-4(6((4(Morpholinomethyl)Phenyl)Ethynyl)-3-Oxo-1H-Pyrrolo[1,2-C]Imidazol-2(3H)Yl)Butanamide
Organism: Pseudomonas aeruginosa lesb58
Method: X-RAY DIFFRACTION Resolution:1.94 Å Release Date: 2019-12-18 Classification: HYDROLASE Ligands: ZN, H2Z |
Organism: Pseudomonas aeruginosa lesb58
Method: X-RAY DIFFRACTION
Release Date: 2019-12-18
Ligands: ZN, H2Z
 |
Structure Of P. Aeruginosa Lpxc With Compound 18D: (2R)-N-Hydroxy-4-(6-((1-(Hydroxymethyl)Cyclopropyl)Buta-1,3-Diyn-1-Yl)-3-Oxo-1H-Pyrrolo[1,2-C]Imidazol-2(3H)-Yl)-2-Methyl-2-(Methylsulfonyl)Butanamide
Organism: Pseudomonas aeruginosa lesb58
Method: X-RAY DIFFRACTION Resolution:2.25 Å Release Date: 2019-12-18 Classification: HYDROLASE Ligands: ZN, H2Q |
Organism: Pseudomonas aeruginosa lesb58
Method: X-RAY DIFFRACTION
Release Date: 2019-12-18
Ligands: ZN, H2Q
 |
E. Coli Dna Gyrase B 24 Kda Atpase Domain In Complex With 1-Ethyl-3-[8-Methyl-5-(2-Methyl-Pyridin-4-Yl)-Isoquinolin-3-Yl]-Urea
Organism: Escherichia coli o157:h7
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2017-04-26 Classification: ISOMERASE Ligands: O54 |
Organism: Escherichia coli o157:h7
Method: X-RAY DIFFRACTION
Release Date: 2017-04-26
Ligands: O54
 |
E. Coli Dna Gyrase B 24 Kda Atpase Domain In Complex With [3-(3-Ethyl-Ureido)-5-(Pyridin-4-Yl)-Isoquinolin-8-Yl-Methyl]-Carbamic Acid Prop-2-Ynyl Ester
Organism: Escherichia coli o157:h7
Method: X-RAY DIFFRACTION Resolution:1.81 Å Release Date: 2017-04-26 Classification: ISOMERASE Ligands: 9JG, PO4 |
Organism: Escherichia coli o157:h7
Method: X-RAY DIFFRACTION
Release Date: 2017-04-26
Ligands: 9JG, PO4
 |
E. Coli Dna Gyrase B 24 Kda Atpase Domain In Complex With 1-Ethyl-3-[5-Pyridin-4-Yl-8-(Pyridin-3-Ylamino)-Isoquinolin-3-Yl]-Urea
Organism: Escherichia coli o157:h7
Method: X-RAY DIFFRACTION Resolution:2.05 Å Release Date: 2017-04-26 Classification: ISOMERASE Ligands: G3Z |
Organism: Escherichia coli o157:h7
Method: X-RAY DIFFRACTION
Release Date: 2017-04-26
Ligands: G3Z
 |
Dna Ligase A In Complex With Inhibitor
Organism: Streptococcus pneumoniae
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2012-10-10 Classification: LIGASE/LIGASE INHIBITOR Ligands: SO4, 0XT, NMN |
Organism: Streptococcus pneumoniae
Method: X-RAY DIFFRACTION
Release Date: 2012-10-10
Ligands: SO4, 0XT, NMN
 |
Dna Ligase A In Complex With Inhibitor
Organism: Escherichia coli, Synthetic construct
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2012-10-10 Classification: LIGASE/LIGASE INHIBITOR/DNA Ligands: ZN, SO4, 0XS |
Organism: Escherichia coli, Synthetic construct
Method: X-RAY DIFFRACTION
Release Date: 2012-10-10
Ligands: ZN, SO4, 0XS
 |
Factor Xa - Cation Inhibitor Complex
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.25 Å Release Date: 2009-01-13 Classification: HYDROLASE Ligands: BI7, CA, NA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-01-13
Ligands: BI7, CA, NA
 |
Complex Of Recombinant Human Thrombin With A Designed Inhibitor
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION Resolution:1.30 Å Release Date: 2006-11-06 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: F25, NA, CA |
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION
Release Date: 2006-11-06
Ligands: F25, NA, CA
 |
Complex Of Recombinant Human Thrombin With An Inhibitor
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION Resolution:1.30 Å Release Date: 2006-06-14 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ESH, NA, CA |
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION
Release Date: 2006-06-14
Ligands: ESH, NA, CA
 |
Complex Of Recombinant Human Thrombin With An Inhibitor
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION Resolution:1.79 Å Release Date: 2006-06-14 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 348, NA, CA |
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION
Release Date: 2006-06-14
Ligands: 348, NA, CA
 |
Complex Of Thrombin With Designed Inhibitor 7165
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION Resolution:1.54 Å Release Date: 2005-06-20 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: SHY, NA, CA |
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION
Release Date: 2005-06-20
Ligands: SHY, NA, CA
 |
Complex Of Recombinant Human Thrombin With A Designed Fluorinated Inhibitor
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION Resolution:1.67 Å Release Date: 2003-06-24 Classification: HYDROLASE/HYDROLASE INHIBITOR |
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION
Release Date: 2003-06-24