Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2009 Jan;108(2):331–340. doi: 10.1111/j.1471-4159.2008.05761.x

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

Journal compilation © 2009 International Society for Neurochemistry

Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.

PMC Copyright notice

Fig. 4 — PMA potentiation can be abolished by cysteine substitution of amino terminal residues. (a) Sample traces of ATP evoked currents (100 μM application indicated by bar) from oocytes under control conditions and following PMA (100 nM) treatment for WT as well as the mutants D17C, N26C and K27C. (b) Summary of the percentage changes of peak amplitudes by PMA treatment for N-termini cysteine mutants. Cysteine mutants around the conserved PKC consensus site and next to the first transmembrane segment were no longer potentiated by PMA. (c) Effects of mutations of the minigene on PMA potentiation. **p< 0.01, ***p< 0.001.