Key points are not available for this paper at this time.
We have described a structural scaffold extant in over 500 homologous enzymes, where the catalytic mechanism is identical and the substrate specificity varied. The many known structures of chymotrypsin-fold serine proteases delineate a clear framework showing that this variability is a function of evolved diversity in the structures of surface loops, which surround the extended substrate binding site. Because the loops are conserved in their relative positions with respect to the N to C direction of the scissile peptide, general themes for their individual functions can be described. Thus, loop C is invariably positioned to directly contact the extended substrate on the N-terminal side of the scissile bond, whereas loops A, B, D, and E interact on the leaving group side (Fig. 3). Loops 2 and 3 can modulate either or both of the S1 sites or the subsite preferences on the N-terminal side of the scissile bond. Loop 1 is thus far known to determine only the S1 site specificity.
Building similarity graph...
Analyzing shared references across papers
Loading...
John J. Perona
Charles S. Craik
Journal of Biological Chemistry
University of California, San Francisco
University of California, Santa Barbara
Building similarity graph...
Analyzing shared references across papers
Loading...
Perona et al. (Sat,) studied this question.
www.synapsesocial.com/papers/6a078c46b2d9a7d54307a19d — DOI: https://doi.org/10.1074/jbc.272.48.29987
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: