Search Count: 6
 |
Design, Synthesis, And Biological Evaluation Of Pyrazolopyridine-Sulfonamides As Potent Multiple-Mitotic Kinase (Mmk) Inhibitors (Part I)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.90 Å Release Date: 2011-08-10 Classification: transferase/transferase inhibitor Ligands: D36, MG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-08-10
Ligands: D36, MG
 |
Design, Synthesis, And Biological Evaluation Of Pyrazolopyridine-Sulfonamides As Potent Multiple-Mitotic Kinase (Mmk) Inhibitors (Part I)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.90 Å Release Date: 2011-08-10 Classification: transferase/transferase inhibitor Ligands: D37 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-08-10
Ligands: D37
 |
Crystal Structure Of The Complex Between Mmp-8 And A Non-Zinc Chelating Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2009-03-03 Classification: HYDROLASE Ligands: CA, ZN, AXA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-03-03
Ligands: CA, ZN, AXA
 |
Crystal Structure Of The Complex Between Mmp-8 And A Non-Zinc Chelating Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2009-03-03 Classification: HYDROLASE Ligands: CA, ZN, AXB |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-03-03
Ligands: CA, ZN, AXB
 |
Crystal Structure Of The Complex Between Mmp-8 And A Non-Zinc Chelating Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2009-03-03 Classification: HYDROLASE Ligands: CA, ZN, AXB, HAE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-03-03
Ligands: CA, ZN, AXB, HAE
 |
Structure Of Fpt Bound To The Inhibitor Sch66336
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2003-10-21 Classification: transferase/transferase inhibitor Ligands: ZN, FPP, 336 |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2003-10-21
Ligands: ZN, FPP, 336