Skip to main content
. 2009 Mar 3;5(2):139–149. doi: 10.1007/s11302-009-9135-5

Table 1.

Summary of mutant phenotypes

Residues corresponding to those analyzed in this study
mP2X7 hP2X7 hP2X1 rP2X2 rP2X4
R53K R53 T57 D57 E56
R125K R125 G123 H120A A122
R151K R151 K148 H146 R148
R178K R178 R175 N173 Q175
R206K R206 R202A K200 K203
R230K R230 Q231 K228A R231
R276K R276H H277 R274 R277
R277K R277 G278 R275 R278K
R294K R294 R292A R290A R295
R307K R307Q R305A R304A R309
R316K R316 R314A R313 R318K
Other positively charged residues with altered ATP potency
K64 K64 K68A K69A K67
K66 K66 K70A K71A K69
K193 K193A K190A K188A K190R
K311 K311A K309A K308A K313

Italics mutants with no or only small changes in ATP sensitivity, bold mutants with strongly reduced ATP potency, bold italics and underlined gain-of-function mutants, upright (without emphasis) residues that to our knowledge have not been tested by mutagenesis. References for: human P2X7 [53, 60, 74], human P2X1 [51], rat P2X2 [52, 64, 75], and rat P2X4 [65]