Search Count: 32
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The Crystal Structure Of Sph At 0.8A
Organism: Bacillus sphaericus
Method: X-RAY DIFFRACTION Resolution:0.80 Å Release Date: 2009-04-28 Classification: HYDROLASE Ligands: CA |
Organism: Bacillus sphaericus
Method: X-RAY DIFFRACTION
Release Date: 2009-04-28
Ligands: CA
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Phers From Staphylococcus Haemolyticus- Rational Protein Engineering And Inhibitor Studies
Organism: Staphylococcus haemolyticus
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2007-11-06 Classification: LIGASE Ligands: ZN, GAX |
Organism: Staphylococcus haemolyticus
Method: X-RAY DIFFRACTION
Release Date: 2007-11-06
Ligands: ZN, GAX
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Phers From Staphylococcus Haemolyticus- Rational Protein Engineering And Inhibitor Studies
Organism: Staphylococcus haemolyticus
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2007-11-06 Classification: LIGASE Ligands: GAX, SO4, ZN |
Organism: Staphylococcus haemolyticus
Method: X-RAY DIFFRACTION
Release Date: 2007-11-06
Ligands: GAX, SO4, ZN
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Sphericase
Organism: Bacillus sphaericus
Method: X-RAY DIFFRACTION Resolution:0.80 Å Release Date: 2007-08-21 Classification: HYDROLASE Ligands: CA |
Organism: Bacillus sphaericus
Method: X-RAY DIFFRACTION
Release Date: 2007-08-21
Ligands: CA
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S41 Psychrophilic Protease
Organism: Bacillus subtilis
Method: X-RAY DIFFRACTION Resolution:1.40 Å Release Date: 2007-05-01 Classification: HYDROLASE Ligands: CA, NA, PMS |
Organism: Bacillus subtilis
Method: X-RAY DIFFRACTION
Release Date: 2007-05-01
Ligands: CA, NA, PMS
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Crystal Structure Of Ppar Gamma With N-Sulfonyl-2-Indole Carboxamide Ligands
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2006-09-19 Classification: TRANSCRIPTION Ligands: NSI |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2006-09-19
Ligands: NSI
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Hck Kinase In Complex With Lck Targetted Inhibitor Pg-1009247
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2006-09-05 Classification: TRANSFERASE Ligands: 1BM |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2006-09-05
Ligands: 1BM
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Engineering The Ptpbeta Catalytic Domain With Improved Crystallization Properties
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2006-09-05 Classification: HYDROLASE Ligands: CL, UA5, MG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2006-09-05
Ligands: CL, UA5, MG
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Engineered Catalytic Domain Of Protein Tyrosine Phosphatase Hptpbeta
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2006-08-29 Classification: HYDROLASE Ligands: CL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2006-08-29
Ligands: CL
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Structural Studies Of Protein Tyrosine Phosphatase Beta Catalytic Domain In Complex With Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2006-08-29 Classification: HYDROLASE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2006-08-29
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Structural Studies Of Protein Tyrosine Phosphatase Beta Catalytic Domain In Complex With Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.75 Å Release Date: 2006-08-29 Classification: HYDROLASE Ligands: VO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2006-08-29
Ligands: VO4
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Structural Studies Of Protein Tyrosine Phosphatase Beta Catalytic Domain In Complex With A Sulfamic Acid (Soaking Experiment)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.65 Å Release Date: 2006-08-29 Classification: HYDROLASE Ligands: CL, UA1 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2006-08-29
Ligands: CL, UA1
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Structural Studies Of Protein Tyrosine Phosphatase Beta Catalytic Domain Co-Crystallized With A Sulfamic Acid Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.15 Å Release Date: 2006-08-29 Classification: HYDROLASE Ligands: MG, CL, UA1 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2006-08-29
Ligands: MG, CL, UA1
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Mutated Map Kinase P38 (Mus Musculus) In Complex With Inhbitor Pg-951717
Organism: Mus musculus
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2006-07-11 Classification: TRANSFERASE Ligands: SO4, LIE |
Organism: Mus musculus
Method: X-RAY DIFFRACTION
Release Date: 2006-07-11
Ligands: SO4, LIE
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Crystal Structure Of Hif Prolyl Hydroxylase Egln-1 In Complex With A Biologically Active Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2006-06-27 Classification: OXIDOREDUCTASE Ligands: FE2, UN9 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2006-06-27
Ligands: FE2, UN9
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Crystal Structure Of Hif Prolyl Hydroxylase Egln-1 In Complex With A Biologically Active Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2006-06-27 Classification: OXIDOREDUCTASE Ligands: FE2, UN9 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2006-06-27
Ligands: FE2, UN9
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Engineered Catalytic Domain Of Protein Tyrosine Phosphatase Hptpbeta.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.30 Å Release Date: 2006-06-27 Classification: HYDROLASE Ligands: ACT, CL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2006-06-27
Ligands: ACT, CL
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Engineered Protein Tyrosine Phosphatase Beta Catalytic Domain
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.40 Å Release Date: 2006-06-27 Classification: HYDROLASE Ligands: MG, NA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2006-06-27
Ligands: MG, NA
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Novel Bacterial Methionine Aminopeptidase Inhibitors
Organism: Escherichia coli k12
Method: X-RAY DIFFRACTION Resolution:1.28 Å Release Date: 2006-06-13 Classification: HYDROLASE Ligands: CO, NA, U11 |
Organism: Escherichia coli k12
Method: X-RAY DIFFRACTION
Release Date: 2006-06-13
Ligands: CO, NA, U11
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Novel Bacterial Methionine Aminopeptidase Inhibitors
Organism: Escherichia coli k12
Method: X-RAY DIFFRACTION Resolution:1.00 Å Release Date: 2006-06-13 Classification: HYDROLASE Ligands: CO, NA, U12 |
Organism: Escherichia coli k12
Method: X-RAY DIFFRACTION
Release Date: 2006-06-13
Ligands: CO, NA, U12