Table 3.
Comparison | θ1 ± S.Ea | Pb | Qk>0.70c | Critical amino acid sitesd |
Sub. I vs II | 0.220 ± 0.056 | <0.01 | 7 | 35*, 65, 70*, 110, 258*, 306, 324* |
Sub. I vs III | 0.280 ± 0.055 | <0.01 | 11 | 41*, 54, 69*, 80, 104, 243*, 258*, 312, 324*, 330*, 360 |
Sub. I vs IV | 0.176 ± 0.070 | <0.01 | 1 | 212 |
Sub. I vs V | 0.351 ± 0.083 | <0.01 | 7 | 62*, 98, 166, 212, 227*, 254*, 264 |
Sub. I vs VI | 0.229 ± 0.063 | <0.01 | 5 | 47, 110, 157*, 212, 307* |
Sub. I vs VII | 0.377 ± 0.077 | <0.01 | 16 | 38, 43, 56*, 62*, 68, 85, 163*, 178, 207*, 227*, 245, 257,258*, 327*, 331, 332 |
Sub. II vs III | 0.340 ± 0.064 | <0.01 | 14 | 41*, 65, 69*, 70*, 80, 85, 167, 169, 194, 201, 243*, 306, 308, 309 |
Sub. II vs IV | 0.001 ± 0.022 | >0.05 | 0 | Not found |
Sub. II vs V | 0.142 ± 0.133 | >0.05 | 0 | Not found |
Sub. II vs VI | 0.269 ± 0.064 | <0.01 | 10 | 38, 65, 157*, 191, 223, 245, 248*, 307*, 308, 324* |
Sub. II vs VII | 0.114 ± 0.083 | <0.05 | 0 | Not found |
Sub. III vs IV | 0.350 ± 0.086 | <0.01 | 8 | 21, 40*, 83*, 187, 254*, 307*, 308, 309 |
Sub. III vs V | 0.437 ± 0.084 | <0.01 | 16 *62, 66, 70*, 82, 104, 158*, 176, 243*, 254*, 255, 258*, 264, 273, 275, 318, 330* | |
Sub. III vs VI | 0.353 ± 0.068 | <0.01 | 13 | 21, 70*, 87, 158*, 243*, 248*, 255, 259, 309, 312, 314*, 318, 324* |
Sub. III vs VII | 0.378 ± 0.081 | <0.01 | 12 | 56*, 62*, 68, 69*, 85, 189, 205*, 228*, 233, 245, 324*, 330* |
Sub. IV vs V | 0.288 ± 0.155 | <0.05 | 0 | Not found |
Sub. IV vs VI | 0.351 ± 0.083 | <0.01 | 9 | 47, 157*, 189, 223, 248*, 254*, 265, 307*, 308 |
Sub. IV vs VII | 0.259 ± 0.153 | <0.05 | 0 | Not found |
Sub. V vs VI | 0.159 ± 0.105 | >0.05 | 0 | Not found |
Sub. V vs VII | 0.316 ± 0.162 | <0.05 | 2 | 264, 332 |
Sub. VI vs VII | 0.178 ± 0.072 | <0.01 | 1 | 245 |
a θ is the coefficient of functional divergence; θ1 ± S.E. is the coefficient of type I functional divergence between two clusters and its standard error.
b The significance level (P value) is computed using Fisher's transformation.
c Qk, posterior probability. A site-specific profile based on the posterior probability (Qk) was used to identify critical amino acid residues that were responsible for functional divergence.
d Numbering of amino acid residues corresponds to AtOPR02-1. Critical amino acid sites with the highest posterior values (Qk>0.70) are shown.
* The amino acid residues depicted with an asterisk were also found to be predicted in positive-selection sites between OPR paralogues (see Table 2).