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文献和实验Methods for Studying the Interaction of Barnase with Its Inhibitor Barstar
complex, with K d =10−14 M , half-life of about 2 d and an association rate constant of 4�108 M −1 /s. The kinetic and thermodynamics of the barnase-barstar interaction were investigated in detail (12 –20 ). High affinity is maintained at pH 7.0–
Identification, Assay, and Functional Analysis of the Antizyme Inhibitor Family
), whose synthesis is stimulated by polyamines. Az inactivates Ornithine decarboxylase [(ODC), the first key enzyme in the polyamine biosynthetic pathway] and marks it for ubiquitin-independent degradation by the 26S proteasome. In addition, Az inhibits uptake
Kaposi’s sarcoma-associated herpesvirus (KSHV) is the etiological agent of Kaposi’s sarcoma (KS), the most common cancer in AIDS patients. All herpesviruses express a conserved dimeric serine protease that is required for generating
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