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. 1990 Nov 30;173(1):276-82.
doi: 10.1016/s0006-291x(05)81053-8.

Effects of herbimycin A and various SH-reagents on p60v-src kinase activity in vitro

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Effects of herbimycin A and various SH-reagents on p60v-src kinase activity in vitro

H Fukazawa et al. Biochem Biophys Res Commun. .

Abstract

Herbimycin A is an antiobiotic which reverses transformation caused by src family oncogenes. It inactivates p60v-src in vitro, possibly by binding to reactive SH-group(s) of the kinase. We examined effects of various SH-reagents on p60v-src and observed that N-[p-(2-benzimidazolyl)phenyl]maleimide (BIPM) or N-(9-acridinyl)maleimide (NAM) were potent inactivators of the kinase, whereas N-ethylmaleimide (NEM) required high concentrations, and iodoacetamide was totally ineffective in reducing the kinase activity. Pretreatment of p60v-src immune-complex with NEM and iodoacetamide, however, protected the kinase from inactivation by herbimycin A, BIPM, and NAM. The results suggest that SH-group(s) to which herbimycin A binds is not essential for the kinase activity, but is positioned in the vicinity of the active center.

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