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  1. From X-ray crystallographic structure to intrinsic thermodynamics of protein–ligand binding using carbonic anhydrase isozymes as a model system
  2. Thiazide and other Cl-benzenesulfonamide-bearing clinical drug affinities for human carbonic anhydrases
  3. Experimental Approaches to Identify Selective Picomolar Inhibitors for Carbonic Anhydrase IX
  4. POT1 stability and binding measured by fluorescence thermal shift assays
  5. Structural details of the enzymatic catalysis of carbonic anhydrase II via a mutation of valine to isoleucine
  6. Binding affinity in drug design: experimental and computational techniques
  7. Thermodynamic, kinetic, and structural parameterization of human carbonic anhydrase interactions toward enhanced inhibitor design
  8. Intrinsic binding of 4-substituted-2,3,5,6-tetrafluorobenezenesulfonamides to native and recombinant human carbonic anhydrase VI
  9. Inhibitor Binding to Hsp90: A Review of Thermodynamic, Kinetic, Enzymatic, and Cellular Assays