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. Author manuscript; available in PMC: 2007 Aug 20.
Published in final edited form as: Biochim Biophys Acta. 2007 Feb 17;1773(6):707–717. doi: 10.1016/j.bbamcr.2007.02.002

Table 3.

Relative activity in a growth arrest assay of STE2 alleles containing substitutions at extracellular charged groups

Yeast strain STE2 allele Relative activity*
A448 STE2+ 100
A2360 D3A 56 ± 10
A2361 D14A 49 ± 6**
A2362 D39A 51 ± 7**
A2363 E40A 55 ± 7**
A2364 D124A 50 ± 6**
A2365 D195A 48 ± 6**
A2366 D201A 46 ± 5**
A2367 D275A N.D.
A2798 D3N 79 ± 12
A2799 D14N 70 ± 10
A2800 D39N 77 ± 11
A2801 E40Q 76 ± 11
A2802 D124N 87 ± 13
A2803 D195N 82 ± 11**
A2804 D201N 73 ± 13
A2805 D275N N.D.
A3081 K100A 89 ± 15
A3082 R122A 106 ± 18
A3083 H126A 144 ± 8
A3084 K187A 136 ± 24
A3085 K202A 95 ± 16
A3086 K269A 101 ± 26
*

Relative activity is calculated as: (α-factor required to produce a 15 mm halo in the wild type Ste2p/α-factor required to produce a 15 mm halo in the mutant alleles) × 100.The values are expressed as mean ± SEM of at least three independent experiments.

**

The change activity for these alleles (compared with STE2+) was statistically significant at the level of p<0.05.

N.D., Not Determined; Halos for this strain had indistinct edges and had smaller diameters than halos for strains expressing wild-type receptors.

N.D., Not Determined; Halos for this strain had indistinct edges but were approximately the same size as the halos of strains expressing wild-type receptors.