Search Count: 12
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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
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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: P55 |
Organism: Zea mays
Method: X-RAY DIFFRACTION
Release Date: 2008-05-13
Ligands: P55
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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:2.00 Å Release Date: 2008-05-13 Classification: TRANSFERASE Ligands: P29 |
Organism: Zea mays
Method: X-RAY DIFFRACTION
Release Date: 2008-05-13
Ligands: P29
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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:2.00 Å Release Date: 2008-05-13 Classification: TRANSFERASE Ligands: P63 |
Organism: Zea mays
Method: X-RAY DIFFRACTION
Release Date: 2008-05-13
Ligands: P63
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Crystal Structure Of The Catalytic Fragment Of Poly (Adp-Ribose) Polymerase Complexed With A Benzimidazole Inhibitor
Organism: Gallus gallus
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2001-01-17 Classification: TRANSFERASE Ligands: BZC |
Organism: Gallus gallus
Method: X-RAY DIFFRACTION
Release Date: 2001-01-17
Ligands: BZC
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2.3 Angstroms Crystal Structure Of The Catalytic Domain Of Dna Polymerase Beta
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 1995-01-26 Classification: NUCLEOTIDYLTRANSFERASE |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 1995-01-26
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Structures Of Apo And Complexed Escherichia Coli Glycinamide Ribonucleotide Transformylase
Organism: Escherichia coli
Method: X-RAY DIFFRACTION Resolution:2.80 Å Release Date: 1993-10-31 Classification: TRANSFERASE(FORMYL) Ligands: PO4 |
Organism: Escherichia coli
Method: X-RAY DIFFRACTION
Release Date: 1993-10-31
Ligands: PO4
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Structures Of Apo And Complexed Escherichia Coli Glycinamide Ribonucleotide Transformylase
Organism: Escherichia coli
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 1993-10-31 Classification: TRANSFERASE(FORMYL) Ligands: GAR, DZF |
Organism: Escherichia coli
Method: X-RAY DIFFRACTION
Release Date: 1993-10-31
Ligands: GAR, DZF
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Refined Atomic Model Of Glutamine Synthetase At 3.5 Angstroms Resolution
Organism: Salmonella typhimurium
Method: X-RAY DIFFRACTION Resolution:3.50 Å Release Date: 1989-10-15 Classification: LIGASE(AMIDE SYNTHETASE) Ligands: MN |
Organism: Salmonella typhimurium
Method: X-RAY DIFFRACTION
Release Date: 1989-10-15
Ligands: MN