Search Count: 20
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The Structure Of Mouse Asterc (Gramd1C) With Ezetimibe
Organism: Mus musculus
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2023-09-13 Classification: LIPID TRANSPORT Ligands: GOL, EOH, CL, PGE, H56 |
Organism: Mus musculus
Method: X-RAY DIFFRACTION
Release Date: 2023-09-13
Ligands: GOL, EOH, CL, PGE, H56
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Crystal Structure Of Taga With Udp-Glcnac
Organism: Thermoanaerobacter italicus (strain dsm 9252 / ab9)
Method: X-RAY DIFFRACTION Resolution:2.99 Å Release Date: 2021-12-29 Classification: TRANSFERASE Ligands: UD1 |
Organism: Thermoanaerobacter italicus (strain dsm 9252 / ab9)
Method: X-RAY DIFFRACTION
Release Date: 2021-12-29
Ligands: UD1
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Crystal Structure Of Taga With Udp-Mannac
Organism: Thermoanaerobacter italicus (strain dsm 9252 / ab9)
Method: X-RAY DIFFRACTION Resolution:3.30 Å Release Date: 2021-12-29 Classification: TRANSFERASE Ligands: UD9 |
Organism: Thermoanaerobacter italicus (strain dsm 9252 / ab9)
Method: X-RAY DIFFRACTION
Release Date: 2021-12-29
Ligands: UD9
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Structure Of Mouse Asterc (Gramd1C) With A New Cholesterol-Derived Compound
Organism: Mus musculus
Method: X-RAY DIFFRACTION Resolution:2.09 Å Release Date: 2021-01-13 Classification: LIPID TRANSPORT Ligands: YK8, EOH, GOL |
Organism: Mus musculus
Method: X-RAY DIFFRACTION
Release Date: 2021-01-13
Ligands: YK8, EOH, GOL
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Crystal Structure Of Human Dhodh With Osu-03012
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.40 Å Release Date: 2019-11-13 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: ORO, FMN, SO4, M4J |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-11-13
Ligands: ORO, FMN, SO4, M4J
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Crystal Structure Of Human Dhodh With Tak-632
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 2019-11-13 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: ORO, FMN, PO4, 1SU |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-11-13
Ligands: ORO, FMN, PO4, 1SU
 |
Solution Structure Of The Bacillus Anthracis Sortase A-Substrate Complex
Organism: Bacillus anthracis str. sterne, Synthetic
Method: SOLUTION NMR Release Date: 2015-09-09 Classification: HYDROLASE/HYDROLASE SUBSTRATE |
Organism: Bacillus anthracis str. sterne, Synthetic
Method: SOLUTION NMR
Release Date: 2015-09-09
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Human Dck C4S-S74E Mutant In Complex With Udp And The Inhibitor 6 {2-[5-(4-{[(4,6-Diaminopyrimidin-2-Yl)Sulfanyl]Methyl}-5-Propyl-1,3-Thiazol-2-Yl)-2-Methoxyphenoxy]Ethanol}
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2015-02-18 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 2XZ, UDP |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-02-18
Ligands: 2XZ, UDP
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Human Dck C4S-S74E Mutant In Complex With Udp And The Inhibitor 7 {N-(2-(3-(4-(((4,6-Diaminopyrimidin-2-Yl)Thio)Methyl)-5-Propylthiazol-2-Yl)Phenoxy)Ethyl)Methanesulfonamide}
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.15 Å Release Date: 2015-02-18 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 2Y0, UDP |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-02-18
Ligands: 2Y0, UDP
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Human Dck C4S-S74E Mutant In Complex With Udp And The Inhibitor 9 {2-{[(1R)-1-{2-[3-(2-Fluoroethoxy)-4-Methoxyphenyl]-5-Propyl-1,3-Thiazol-4-Yl}Ethyl]Sulfanyl}Pyrimidine-4,6-Diamine}
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2015-02-18 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 2Y1, UDP |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-02-18
Ligands: 2Y1, UDP
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Human Dck C4S-S74E Mutant In Complex With Udp And The Inhibitor 4 [1-[5-(4-{[(2,6-Diaminopyrimidin-4-Yl)Sulfanyl]Methyl}-5-Propyl-1,3-Thiazol-2-Yl)-2-Methoxyphenoxy]-2-Methylpropan-2-Ol]
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2014-11-05 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 2XJ, UDP |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-11-05
Ligands: 2XJ, UDP
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Human Dck C4S-S74E Mutant In Complex With Udp And The Inhibitor 5 {5-(4-{[(4,6-Diaminopyrimidin-2-Yl)Sulfanyl]Methyl}-5-Propyl-1,3-Thiazol-2-Yl)-2-Methoxyphenol}
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.09 Å Release Date: 2014-11-05 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 2XL, UDP |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-11-05
Ligands: 2XL, UDP
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Human Dck C4S-S74E Mutant In Complex With Udp And The Inhibitor 8 {2,2'-[{4-[(2R)-4-{[(4,6-Diaminopyrimidin-2-Yl)Sulfanyl]Methyl}-5-Propyl-2,3-Dihydro-1,3-Thiazol-2-Yl]Benzene-1,2-Diyl}Bis(Oxy)]Diethanol}
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2014-11-05 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 2XM, UDP |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-11-05
Ligands: 2XM, UDP
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Human Dck C4S-S74E Mutant In Complex With Udp And The Inhibitor 10 {2-{[(1R/S)-1-{2-[3-(2-Fluoroethoxy)-4-Methoxyphenyl]-5-Methyl-1,3-Thiazol 4-Yl}Ethyl]Sulfanyl}Pyrimidine-4,6-Diamine}
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2014-11-05 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 2Y8, 2Y7, UDP |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-11-05
Ligands: 2Y8, 2Y7, UDP
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Human Dck C4S-S74E Mutant In Complex With Udp And The Inhibitor 12R {N-{2-[5-(4-{(1R)-1-[(4,6-Diaminopyrimidin-2-Yl)Sulfanyl]Ethyl}-5-Methyl-1,3-Thiazol-2-Yl)-2-Methoxyphenoxy]Ethyl}Methanesulfonamide}
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2014-11-05 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: UDP, 2XN |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-11-05
Ligands: UDP, 2XN
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Human Dck C4S-S74E Mutant In Complex With Udp And The Di-39 Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.09 Å Release Date: 2014-03-12 Classification: transferase/transferase inhibitor Ligands: 1QC, UDP |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-03-12
Ligands: 1QC, UDP
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Staphylococcus Aureus Sortase B-Substrate Complex
Organism: Staphylococcus aureus
Method: X-RAY DIFFRACTION Resolution:2.49 Å Release Date: 2014-02-12 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: SO4 |
Organism: Staphylococcus aureus
Method: X-RAY DIFFRACTION
Release Date: 2014-02-12
Ligands: SO4
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Human Dck C4S-S74E Mutant In Complex With Udp And The F2.2.1 Inhibitor (2-[({2-[3-(2-Fluoroethoxy)-4-Methoxyphenyl]-5-Methyl-1,3-Thiazol-4-Yl}Methyl)Sulfanyl]Pyrimidine-4,6-Diamine)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.89 Å Release Date: 2013-09-18 Classification: transferase/transferase inhibitor Ligands: UDP, 1NO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-09-18
Ligands: UDP, 1NO
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Human Dck C4S-S74E Mutant In Complex With Udp And The Di-43 Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.94 Å Release Date: 2013-09-18 Classification: transferase/transferase inhibitor Ligands: 1UX, UDP |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-09-18
Ligands: 1UX, UDP
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Solution Structure Of The S. Aureus Sortase A-Substrate Complex
Organism: Staphylococcus aureus
Method: SOLUTION NMR Release Date: 2009-07-21 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: CA |
Organism: Staphylococcus aureus
Method: SOLUTION NMR
Release Date: 2009-07-21
Ligands: CA