a-lytic protease is a 198 amino acid bacterial serine protease that is secreted from Lysobacter enzymogenes. Before secretion it exists as a 40 kD precursor, consisting of a signal sequence, a PRO region, and the mature domain that eventually becomes the active protease. A number of studies have shown that the PRO region is required both in vitro and in vivo for proper folding of a-lytic protease. In vivo the protease expressed without the PRO region is not secreted. In vitro the denatured protease will not refold without the addition of PRO region. The PRO region is also a sub-nanomolar inhibitor of the native enzyme. It is clear that the interactions between the PRO region and the mature protease are extensive and may shed some light on how proteins fold and why a-lytic cannot fold by itself. We will be studying crystals of the PRO region.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR001209-22
Application #
6437491
Study Section
Project Start
2001-03-01
Project End
2002-02-28
Budget Start
Budget End
Support Year
22
Fiscal Year
2001
Total Cost
$143,176
Indirect Cost
Name
Stanford University
Department
Type
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
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