| Literature DB >> 1541261 |
Abstract
The substrate-like 'canonical' inhibition by the 'small' serine proteinase inhibitors and the product-like inhibition by the carboxypeptidase inhibitor have provided the only atomic models of protein inhibitor--proteinase interactions for about 15 years. The recently published structures of cystatin/stefin--papain complexes and of hirudin--thrombin complexes reveal novel non-substrate-like interactions. In addition, the structure of pro-carboxypeptidase shows a model of inactivation which bears resemblance to proteinase/protein inhibitor systems. Considerable progress in understanding the transition between native and cleaved states of the serpins has also been made by several recent structural studies.Entities:
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Year: 1992 PMID: 1541261 DOI: 10.1111/j.1432-1033.1992.tb16654.x
Source DB: PubMed Journal: Eur J Biochem ISSN: 0014-2956