Skip to main content
. 2011 Dec 21;6(12):e29247. doi: 10.1371/journal.pone.0029247

Table 3. Site analysis. Selective pressures and Likelihood-ratio-tests in protamine 1 and protamine 2 sequences.

Protein (domain) N Lc Selective pressures: % class 1 (ω<1) % class 2 (ω = 1) % class 3 (ω>1) Best fit model 2Δl parameter estimates PSS
All sites 41 51 8 M2a (selection) 9.71** p0 = 0.41, p1 = 0.50993, p2 = 0.07950, ω0 = 069, 33C*, 39V
Protamine1 16 153 Anchoring domains 70 16.6 13.3 M8 (beta and ω) 7.34* p0 = 0.58495, p = 0.0050, q = 0.04910, p1 = 0.41505, ω = 2.65844 33C*, 38T*, 39V**
Phosphorylation sites 57.1 28.6 14.3
All sites 63.02 36.98 M1a (neutral) 2.64 p0 = 0.63016, p1 = 0.36984, ω1 = 1.00 not allowed
cleaved-Protamine 2 16 165 Cleaving sites 57.14 42.86 M7 (beta) 3.57 p = 0.09398, q = 0.13753 not allowed
Phosphorylation sites 100 0
All sites 13.32 86.67 M1a (neutral) 2.12 p0 = 0.13325, p1 = 0.86675, ω1 = 1.00 not allowed
mature-Protamine 2 16 162 Anchoring domains 0 100 M7 (beta) 2.52 p = 35.58178, q = 0.00500 not allowed
Phosphorylation sites 0 100

Parameter estimation and likelihood scores under models of variable ω ratios among sites for protamine 1, cleaved region of protamine 2 and the mature form of protamine 2. The data have N sequences, each of Lc codons after alignment gaps are removed. Differences between log-likelihood values of models with 99% statistical significance level for 2 d. f. are indicated in ** and with 95% of statistical significance in *. The proportion of sites under positive selection (p1), or under selective constraint (p0) and parameters p and q for the beta distribution are given. Positively selected sites (PSS) with a posterior probability >0.95 (*) and >0.99 (**) in a Bayes Empirical Bayes are indicated. Selectives pressures are shown as proportion of amino acid sites for different classes of selective regimes. Class 1: sites under purifying selection (0<ω<1); Class 2: sites neutrally evolving (ω = 1); Class 3: sites subject to positive selection or relaxation (ω>1). Proportions of sites in each selective class were also calculated for DNA-anchoring domains, phosphorylation motifs and cleaving sites.