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Mutagenesis of the cysteine-rich clip domain in the Drosophila patterning protease, Snake

*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

A common motif found in invertebrate serine proteases involved in immunity and development is the clip domain, proposed to regulate catalytic activity or protein-protein interactions within proteolytic cascades. Snake functions in a cascade that patterns the Drosophila embryo, and provides an accessible model for exploring the structural requirements for clip domain function. We tested Snake zymogens bearing charged-to-alanine mutations in the clip domain for their ability to rescue embryos lacking endogenous Snake and for their interactions by S2 cell co-transfection with upstream Gastrulation Defective and downstream Easter in the protease cascade. Of 13 single and multiple substitutions, one double mutant in a predicted protruding region exhibited a severe defect in embryonic rescue but showed only minimal defects in the co-transfection assay. We discuss implications of these and other results for potential biological roles of the Snake clip domain and for use of the in vitro assay in predicting protease behavior.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 169-174 (6 pages)

Journal (Volume, Issue Number)

Archives of Biochemistry and Biophysics (Volume 475, Issue 2)

Publication milestones

  • Published - 07/15/2008

Publication status

Published - 07/15/2008

ISSN

0003-9861

Publication IDs

  • Scopus: 44949089390
  • PubMed: 18477463

Publication metrics

Metrics

SciVal
FWCI
0.36
SciVal
Author count
2
SciVal
citations
5
SciVal
Paper percentile
50
Scopus
citations
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
1

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Citation count
5
Captures
9

Funding Details

We thank Maggie Elalayli and Jacklyn Hall for assistance in generating the anti-SNKCAT antibody; Robert DeLotto, David Stein, Donald Morisato, Siegfried Roth, the Bloomington Stock Center, and Exelixis for reagents and fly stocks; and anonymous reviewers for their suggestions. This work was supported by NIH RO1 GM067738 to E.K.L.