Search Count: 25
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Anthrax Lethal Factor Metalloproteinase In Complex With The Hydroxamic Acid Based Small Molecule Pt8421
Organism: Bacillus anthracis
Method: X-RAY DIFFRACTION Resolution:1.63 Å Release Date: 2012-03-14 Classification: HYDROLASE Ligands: ZN, 0LX, MLI |
Organism: Bacillus anthracis
Method: X-RAY DIFFRACTION
Release Date: 2012-03-14
Ligands: ZN, 0LX, MLI
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Crystal Structure Of Bont/A Lc With Zinc Bound
Organism: Clostridium botulinum
Method: X-RAY DIFFRACTION Resolution:2.41 Å Release Date: 2011-04-13 Classification: HYDROLASE Ligands: EDO, ZN |
Organism: Clostridium botulinum
Method: X-RAY DIFFRACTION
Release Date: 2011-04-13
Ligands: EDO, ZN
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Crystal Structure Of Bont/A Lc Complexed With Hydroxamate-Based Inhibitor Pt-1
Organism: Clostridium botulinum
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2011-04-13 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, QI1, EDO |
Organism: Clostridium botulinum
Method: X-RAY DIFFRACTION
Release Date: 2011-04-13
Ligands: ZN, QI1, EDO
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Crystal Structure Of Bont/A Lc Complexed With Hydroxamate-Based Inhibitor Pt-2
Organism: Clostridium botulinum
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2011-04-13 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, QI2, PEG |
Organism: Clostridium botulinum
Method: X-RAY DIFFRACTION
Release Date: 2011-04-13
Ligands: ZN, QI2, PEG
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Crystal Structure Of Bont/A Lc Complexed With Hydroxamate-Based Inhibitor Pt-3
Organism: Clostridium botulinum
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2011-04-13 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, QI3, EDO |
Organism: Clostridium botulinum
Method: X-RAY DIFFRACTION
Release Date: 2011-04-13
Ligands: ZN, QI3, EDO
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Characterization Of The Chk1 Allosteric Inhibitor Binding Site
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.76 Å Release Date: 2009-10-06 Classification: TRANSFERASE Ligands: AGX |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-10-06
Ligands: AGX
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Characterization Of The Chk1 Allosteric Inhibitor Binding Site
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2009-10-06 Classification: TRANSFERASE Ligands: AGY |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-10-06
Ligands: AGY
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Structure-Based Design Of Novel Pin1 Inhibitors (I)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2009-09-22 Classification: ISOMERASE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-09-22
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Structure-Based Design Of Novel Pin1 Inhibitors (I)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2009-09-22 Classification: ISOMERASE Ligands: J9Z |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-09-22
Ligands: J9Z
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Structure-Based Design Of Novel Pin1 Inhibitors (I)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.86 Å Release Date: 2009-09-22 Classification: ISOMERASE Ligands: J8Z |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-09-22
Ligands: J8Z
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Structure Of Haemophilus Influenzae Fabh
Organism: Haemophilus influenzae
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 2009-08-25 Classification: TRANSFERASE |
Organism: Haemophilus influenzae
Method: X-RAY DIFFRACTION
Release Date: 2009-08-25
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Structure Of E. Faecalis Fabh In Complex With Acetyl Coa
Organism: Enterococcus faecalis
Method: X-RAY DIFFRACTION Resolution:3.00 Å Release Date: 2009-08-25 Classification: TRANSFERASE Ligands: ACO |
Organism: Enterococcus faecalis
Method: X-RAY DIFFRACTION
Release Date: 2009-08-25
Ligands: ACO
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Structure Of E. Faecalis Fabh In Complex With 2-({4-Bromo-3-[(Diethylamino)Sulfonyl]Benzoyl}Amino)Benzoic Acid
Organism: Enterococcus faecalis
Method: X-RAY DIFFRACTION Resolution:2.60 Å Release Date: 2009-08-25 Classification: TRANSFERASE Ligands: B82 |
Organism: Enterococcus faecalis
Method: X-RAY DIFFRACTION
Release Date: 2009-08-25
Ligands: B82
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Structure Of E. Faecalis Fabh In Complex With 2-({4-[(3R,5S)-3,5-Dimethylpiperidin-1-Yl]-3-Phenoxybenzoyl}Amino)Benzoic Acid
Organism: Enterococcus faecalis
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2009-08-25 Classification: TRANSFERASE Ligands: B83, SO4 |
Organism: Enterococcus faecalis
Method: X-RAY DIFFRACTION
Release Date: 2009-08-25
Ligands: B83, SO4
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Crystal Structure Of S. Aureus Fabh
Organism: Staphylococcus aureus
Method: X-RAY DIFFRACTION Resolution:2.60 Å Release Date: 2009-08-25 Classification: TRANSFERASE |
Organism: Staphylococcus aureus
Method: X-RAY DIFFRACTION
Release Date: 2009-08-25
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Structure Of E. Coli Fabh
Organism: Escherichia coli k-12
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2009-08-25 Classification: TRANSFERASE |
Organism: Escherichia coli k-12
Method: X-RAY DIFFRACTION
Release Date: 2009-08-25
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Structure-Based Design And Synthesis Of Novel Macrocyclic Pyrazolo[1,5-A] [1,3,5]Triazine Compounds As Potent Inhibitors Of Protein Kinase Ck2 And Their Anticancer Activities
Organism: Zea mays
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2008-11-18 Classification: TRANSFERASE Ligands: P04 |
Organism: Zea mays
Method: X-RAY DIFFRACTION
Release Date: 2008-11-18
Ligands: P04
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Structure-Based Design Of Pyrazolo[1,5-A][1,3,5]Triazine Derivatives As Potent Inhibitors Of Protein Kinase Ck2
Organism: Zea mays
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2008-05-13 Classification: TRANSFERASE Ligands: P19 |
Organism: Zea mays
Method: X-RAY DIFFRACTION
Release Date: 2008-05-13
Ligands: P19
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Structure-Based Design Of Pyrazolo[1,5-A][1,3,5]Triazine Derivatives As Potent Inhibitors Of Protein Kinase Ck2
Organism: Zea mays
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2008-05-13 Classification: TRANSFERASE Ligands: P44 |
Organism: Zea mays
Method: X-RAY DIFFRACTION
Release Date: 2008-05-13
Ligands: P44
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Structure-Based Design Of Pyrazolo[1,5-A][1,3,5]Triazine Derivatives As Potent Inhibitors Of Protein Kinase Ck2
Organism: Zea mays
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2008-05-13 Classification: TRANSFERASE Ligands: P45 |
Organism: Zea mays
Method: X-RAY DIFFRACTION
Release Date: 2008-05-13
Ligands: P45