Search Count: 22
 |
Arginase 2 In Complex With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.62 Å Release Date: 2024-12-04 Classification: HYDROLASE Ligands: MN, A1H0B |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-12-04
Ligands: MN, A1H0B
 |
Arginase 2 In Complex With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.86 Å Release Date: 2024-12-04 Classification: HYDROLASE Ligands: MN, A1H0A |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-12-04
Ligands: MN, A1H0A
 |
Arginase 2 In Complex With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2024-12-04 Classification: HYDROLASE Ligands: MN, DMS, PRO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-12-04
Ligands: MN, DMS, PRO
 |
Arginase 2 In Complex With An Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.76 Å Release Date: 2024-11-27 Classification: HYDROLASE Ligands: MN, A1HZ9 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-11-27
Ligands: MN, A1HZ9
 |
Eed In Complex With Compound 4
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.61 Å Release Date: 2021-12-08 Classification: PROTEIN BINDING Ligands: L9W, 51A |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-12-08
Ligands: L9W, 51A
 |
Eed In Complex With Compound 4
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.39 Å Release Date: 2021-12-08 Classification: PROTEIN BINDING Ligands: L9W, 52R |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-12-08
Ligands: L9W, 52R
 |
Eed In Complex With Compound 4
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.93 Å Release Date: 2021-12-08 Classification: PROTEIN BINDING Ligands: MG, L9W, 54N |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-12-08
Ligands: MG, L9W, 54N
 |
Eed In Complex With A Triazolopyrimidine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.52 Å Release Date: 2019-09-25 Classification: PROTEIN BINDING Ligands: L9W, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-09-25
Ligands: L9W, GOL
 |
Eed In Complex With A Methyl-Thiazole
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2019-09-25 Classification: PROTEIN BINDING Ligands: CA, L9W, L9T |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-09-25
Ligands: CA, L9W, L9T
 |
Novel Inhibitors Of Human Rhinovirus 3C Protease
Organism: Human rhinovirus 2
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2016-06-22 Classification: TRANSFERASE Ligands: GOL, PG4, PGE, HOV |
Organism: Human rhinovirus 2
Method: X-RAY DIFFRACTION
Release Date: 2016-06-22
Ligands: GOL, PG4, PGE, HOV
 |
Novel Inhibitors Of Human Rhinovirus 3C Protease
Organism: Human rhinovirus 2
Method: X-RAY DIFFRACTION Resolution:1.45 Å Release Date: 2016-06-22 Classification: TRANSFERASE Ligands: 6OY |
Organism: Human rhinovirus 2
Method: X-RAY DIFFRACTION
Release Date: 2016-06-22
Ligands: 6OY
 |
S.Aureus Tmk In Complex With A Potent Inhibitor Compound 18, 2-(3-Chlorophenoxy)-3-Methoxy-4-{[(3S)-3-(5-Methyl-2,4-Dioxo-3,4-Dihydropyrimidin-1(2H)-Yl)Piperidin-1-Yl]Methyl}Benzoic Acid
Organism: Staphylococcus aureus subsp. aureus
Method: X-RAY DIFFRACTION Resolution:1.67 Å Release Date: 2014-06-11 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 32K |
Organism: Staphylococcus aureus subsp. aureus
Method: X-RAY DIFFRACTION
Release Date: 2014-06-11
Ligands: 32K
 |
S.Aureus Tmk In Complex With Potent Inhibitor Compound 19, 2-(3-Chlorophenoxy)-3-Fluoro-4-{[(3S)-3-(5-Methyl-2,4-Dioxo-3,4-Dihydropyrimidin-1(2H)-Yl)Piperidin-1-Yl]Methyl}Benzoic Acid
Organism: Staphylococcus aureus subsp. aureus
Method: X-RAY DIFFRACTION Resolution:1.94 Å Release Date: 2014-06-11 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 31Z |
Organism: Staphylococcus aureus subsp. aureus
Method: X-RAY DIFFRACTION
Release Date: 2014-06-11
Ligands: 31Z
 |
S.Aureus Tmk In Complex With The Potent Inhibitor Compound 38, 2-(3-Chlorophenoxy)-3-Methoxy-4-{(1R)-1-[(3S)-3-(5-Methyl-2,4-Dioxo-3,4-Dihydropyrimidin-1(2H)-Yl)Piperidin-1-Yl]Propyl}Benzoic Acid
Organism: Staphylococcus aureus subsp. aureus
Method: X-RAY DIFFRACTION Resolution:1.83 Å Release Date: 2014-06-11 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 32B |
Organism: Staphylococcus aureus subsp. aureus
Method: X-RAY DIFFRACTION
Release Date: 2014-06-11
Ligands: 32B
 |
Tmk In Complex With Compound 46, 2-(3-Chlorophenoxy)-3-Fluoro-4-{(1R)-3-Methyl-1-[(3S)-3-(5-Methyl-2,4-Dioxo-3,4-Dihydropyrimidin-1(2H)-Yl)Piperidin-1-Yl]Butyl}Benzoic Acid
Organism: Staphylococcus aureus subsp. aureus
Method: X-RAY DIFFRACTION Resolution:1.62 Å Release Date: 2014-06-11 Classification: Transferase/transferase inhibitor Ligands: 32C |
Organism: Staphylococcus aureus subsp. aureus
Method: X-RAY DIFFRACTION
Release Date: 2014-06-11
Ligands: 32C
 |
S.Aureus Tmk In Complex With Potent Inhibitor Compound 47
Organism: Staphylococcus aureus subsp. aureus
Method: X-RAY DIFFRACTION Resolution:1.78 Å Release Date: 2014-06-11 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 32E |
Organism: Staphylococcus aureus subsp. aureus
Method: X-RAY DIFFRACTION
Release Date: 2014-06-11
Ligands: 32E
 |
Sulfonylpiperidines As Novel, Antibacterial Inhibitors Of Gram-Positive Thymidylate Kinase (Tmk): Compound 5
Organism: Staphylococcus aureus subsp. aureus
Method: X-RAY DIFFRACTION Resolution:1.55 Å Release Date: 2012-10-31 Classification: transferase/transferase inhibitor Ligands: T05 |
Organism: Staphylococcus aureus subsp. aureus
Method: X-RAY DIFFRACTION
Release Date: 2012-10-31
Ligands: T05
 |
Sulfonylpiperidines As Novel, Antibacterial Inhibitors Of Gram-Positive Thymidylate Kinase (Tmk): Compound 11
Organism: Staphylococcus aureus subsp. aureus
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2012-10-31 Classification: transferase/transferase inhibitor Ligands: 16T |
Organism: Staphylococcus aureus subsp. aureus
Method: X-RAY DIFFRACTION
Release Date: 2012-10-31
Ligands: 16T
 |
Golgi Alpha-Mannosidase Ii Complex With Aminocyclopentitetrol
Organism: Drosophila melanogaster
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2006-12-12 Classification: HYDROLASE Ligands: NAG, ZN, AOL, MPD |
Organism: Drosophila melanogaster
Method: X-RAY DIFFRACTION
Release Date: 2006-12-12
Ligands: NAG, ZN, AOL, MPD
 |
Golgi Alpha-Mannosidase Ii Complex With Benzyl-Aminocyclopentitetrol
Organism: Drosophila melanogaster
Method: X-RAY DIFFRACTION Resolution:1.35 Å Release Date: 2006-12-12 Classification: HYDROLASE Ligands: NAG, ZN, SK3, MPD |
Organism: Drosophila melanogaster
Method: X-RAY DIFFRACTION
Release Date: 2006-12-12
Ligands: NAG, ZN, SK3, MPD