![]() |
JOURNAL TOOLS |
Publishing options |
eTOC |
To subscribe |
Submit an article |
Recommend to your librarian |
ARTICLE TOOLS |
Reprints |
Permissions |
Share |


YOUR ACCOUNT
YOUR ORDERS
SHOPPING BASKET
Items: 0
Total amount: € 0,00
HOW TO ORDER
YOUR SUBSCRIPTIONS
YOUR ARTICLES
YOUR EBOOKS
COUPON
ACCESSIBILITY
REVIEWS
Minerva Biotecnologica 2007 December;19(4):139-50
Copyright © 2007 EDIZIONI MINERVA MEDICA
language: English
Molecular recognition of thermolysin and homologous zinc-metalloproteinases
Khan* M. T. H., Yimingjiang W., Sylte I.
School of Molecular and Structural Biology Institute of Medical Biology Department of Pharmacology Faculty of Medicine, University of Tromsø, Tromsø, Norway
Thermolysin is a thermostable zinc-metalloproteinase secreted by Bacillus thermoproteolyticus and the prototype enzyme of the M4 family of proteinases, which at present consists of 293 family members. These proteinases are secreted from several hundreds of organism and cause lethal infections to mankind. Thermolysin is an attractive target for protein engineering experiments to understand the catalytic mechanism, thermostability, and halophilicity. Thermolysin is very similar in overall structure and active site geometry to angiotensin converting enzyme (ACE) and neprilysin. Thermolysin inhibitors are therefore potential ACE and neprilysin inhibitors and candidates for developing antihypertensive drugs. This paper is a critical review of structural and functional aspects of thermolysin and homologous proteins, and of the present knowledge about thermolysin inhibitors.