Search Count: 11
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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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Crystal Structure Of Human Idh1 In Complex With Gsk321A
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.25 Å Release Date: 2015-10-07 Classification: Oxidoreductase/Oxidoreductase Inhibitor Ligands: NAP, 59D |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-10-07
Ligands: NAP, 59D
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Phosphoinositide-Dependent Kinase-1 (Pdk1) Kinase Domain With 6-(3-Amino-1H-Indazol-6-Yl)-N4-Ethyl-2,4-Pyrimidinediamine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2011-03-09 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: GOL, SO4, 3Q0 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-03-09
Ligands: GOL, SO4, 3Q0
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Phosphoinositide-Dependent Kinase-1 (Pdk1) Kinase Domain With 6-[2-Amino-6-(4-Morpholinyl)-4-Pyrimidinyl]-1H-Indazol-3-Amine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.49 Å Release Date: 2011-03-09 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: GOL, SO4, 3Q1 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-03-09
Ligands: GOL, SO4, 3Q1
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Phosphoinositide-Dependent Kinase-1 (Pdk1) Kinase Domain With 6-{2-Amino-6-[(3R)-3-Methyl-4-Morpholinyl]-4-Pyrimidinyl}-1H-Indazol-3-Amine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2011-03-09 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: GOL, SO4, 3Q2 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-03-09
Ligands: GOL, SO4, 3Q2
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Phosphoinositide-Dependent Kinase-1 (Pdk1) Kinase Domain With 4-[2-Amino-6-(3-Amino-1H-Indazol-6-Yl)-4-Pyrimidinyl]-N-Phenyl-2-Morpholinecarboxamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2011-03-09 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: GOL, SO4, 3Q3 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-03-09
Ligands: GOL, SO4, 3Q3
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Phosphoinositide-Dependent Kinase-1 (Pdk1) Kinase Domain With (2R,5S)-1-[2-Amino-6-(3-Amino-1H-Indazol-6-Yl)-4-Pyrimidinyl]-6-Methyl-N-Phenyl-3-Piperidinecarboxamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.99 Å Release Date: 2011-03-09 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: GOL, SO4, 3Q4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-03-09
Ligands: GOL, SO4, 3Q4
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Phosphoinositide-Dependent Kinase-1 (Pdk1) Kinase Domain With 1,1-Dimethylethyl {(3R,6S)-1-[2-Amino-6-(3-Amino-1H-Indazol-6-Yl)-4-Pyrimidinyl]-6-Methyl-3-Piperidinyl}Carbamate
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2011-03-09 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 3Q5, SO4, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-03-09
Ligands: 3Q5, SO4, GOL
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Phosphoinositide-Dependent Kinase-1 (Pdk1) Kinase Domain With 1,1-Dimethylethyl{(3R,5R)-1-[2-Amino-6-(3-Amino-1H-Indazol-6-Yl)-4-Pyrimidinyl]-5-Methyl-3-Piperidinyl}Carbamate
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2011-03-09 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 3Q6, SO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-03-09
Ligands: 3Q6, SO4