| Literature DB >> 8513441 |
T Hiwasa1, J Fujita-Yoshigaki, M Shirouzu, H Koide, T Sawada, S Sakiyama, S Yokoyama.
Abstract
Protease-inhibitory activity of recombinant Ha-ras gene products (Ras) toward papain and cathepsins B and L was investigated. v-Ha-Ras showed more potent inhibitory activity toward cathepsin B as compared with c-Ha-Ras. We have also investigated protease-inhibitory activity of c-Ha-Ras mutants with point mutations in amino acids between positions 23 and 50. Inhibitory activity of Ras toward papain and cathepsin L was not largely altered among mutants. However, the inhibitory activity toward cathepsin B was significantly impaired by a mutation at position 43, 44, 45 or 48. These results suggest that 43Gln-Val-Val sequence plays an important role at least to inhibit cathepsin B.Entities:
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Year: 1993 PMID: 8513441 DOI: 10.1016/0304-3835(93)90169-a
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679