Client Proteins and Small Molecule Inhibitors Display Distinct Binding Preferences for Constitutive and Stress-Induced HSP90 Isoforms and Their Conformationally Restricted Mutants

客户蛋白和小分子抑制剂对组成型和应激诱导型 HSP90 同工型及其构象受限突变体表现出不同的结合偏好。