Search Count: 8
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Crystal Structure Of Steptococcus Pneumoniae Undecaprenyl Pyrophosphate Synthase (Upps)
Organism: Streptococcus pneumoniae serotype 4 (strain atcc baa-334 / tigr4)
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2016-07-20 Classification: TRANSFERASE |
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Crystal Structure Of Steptococcus Pneumoniae Undecaprenyl Pyrophosphate Synthase (Upps) With Farnesyl Diphosphate
Organism: Streptococcus pneumoniae serotype 4 (strain atcc baa-334 / tigr4)
Method: X-RAY DIFFRACTION Resolution:3.20 Å Release Date: 2016-07-20 Classification: TRANSFERASE Ligands: FPP |
Organism: Streptococcus pneumoniae serotype 4 (strain atcc baa-334 / tigr4)
Method: X-RAY DIFFRACTION
Release Date: 2016-07-20
Ligands: FPP
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Crystal Structure Of Steptococcus Pneumoniae Undecaprenyl Pyrophosphate Synthase (Upps) In Complex With ~{N}-(3-Azanyl-3-Oxidanylidene-Propyl)-5-(1-Benzothiophen-5-Yl)-1-(Phenylmethyl)-~{N}-[(4-Propan-2-Yloxyphenyl)Methyl]Pyrazole-4-Carboxamide
Organism: Streptococcus pneumoniae serotype 4 (strain atcc baa-334 / tigr4)
Method: X-RAY DIFFRACTION Resolution:2.63 Å Release Date: 2016-07-20 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 6TC |
Organism: Streptococcus pneumoniae serotype 4 (strain atcc baa-334 / tigr4)
Method: X-RAY DIFFRACTION
Release Date: 2016-07-20
Ligands: 6TC
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Pi3K Alpha Lipid Kinase With Active Site Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.90 Å Release Date: 2015-06-17 Classification: Transferase/Transferase Inhibitor Ligands: 4EL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-06-17
Ligands: 4EL
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Encoded Library Technology As A Source Of Hits For The Discovery And Lead Optimization Of A Potent And Selective Class Of Bactericidal Direct Inhibitors Of Mycobacterium Tuberculosis Inha
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION Resolution:2.40 Å Release Date: 2014-02-12 Classification: TRANSFERASE Ligands: KV1, NAD |
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION
Release Date: 2014-02-12
Ligands: KV1, NAD
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Crystal Structure Of Human Sirt3 With Elt Inhibitor 11C [N-{2-[1-(6-Carbamoylthieno[3,2-D]Pyrimidin-4-Yl)Piperidin-4-Yl]Ethyl}-N'-Ethylthiophene-2,5-Dicarboxamide]
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2013-04-24 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, 1NQ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-04-24
Ligands: ZN, 1NQ
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Crystal Structure Of Human Sirt3 With Elt Inhibitor 28 [4-(4-{2-[(2,2-Dimethylpropanoyl)Amino]Ethyl}Piperidin-1-Yl)Thieno[3,2-D]Pyrimidine-6-Carboxamide[
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.26 Å Release Date: 2013-04-24 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, 1NR |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-04-24
Ligands: ZN, 1NR
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Crystal Structure Of Human Sirt3 With Elt Inhibitor 3 [14-(4-{2-[(Methylsulfonyl)Amino]Ethyl}Piperidin-1-Yl)Thieno[3,2-D]Pyrimidine-6-Carboxamide]
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.24 Å Release Date: 2013-04-24 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, 1NS, GOL, NA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-04-24
Ligands: ZN, 1NS, GOL, NA