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. 2013 Dec 13;5(12):2488–2503. doi: 10.3390/toxins5122488

Table 1.

Molecular evolution analyses of Trittame loki major ICK toxin clades.

SLAC a FEL b REL c MEME d FUBAR e Integrative f BSR g PAML h
SLAC + FEL + REL + MEME M8 M2a
Clade I ω > 1 i 0 2 22 2 sites 13 22 3 17 12
ω < 1 j 0 4 0 0 4 (9 + 8) (6 + 6)
ω = 1.41 - 1.62 - - 1.81 1.81
Clade II ω > 1 i 0 0 0 0 sites 0 0 4 5 3
ω < 1 j 3 11 0 14 15 (1 + 4) (1 + 2)
ω = 0.42 - 0.47 - - 0.67 0.67

Legend: a: Single Likelihood Ancestor Counting; b: Fixed-effects likelihood; c: Random-effects likelihood; d: Sites detected as experiencing episodic diversifying selection (0.05 significance) by the Mixed Effects Model Evolution (MEME); e: Fast Unconstrained Bayesian AppRoximation; f: Sites detected in common by SLAC, FEL, REL, MEME and FUBAR (the integrative approach); g: Number of branches detected by the branch-site REL (Random effects likelihood) test as episodically diversifying; h: Positively selected sites detected by the Bayes Empirical Bayes approach implemented in M8 and M2a. Sites detected at 0.99 and 0.95 significance are indicated in the parenthesis; i: Number of positively selected sites at 0.05 significance (for SLAC, FEL) or 50 Bayes factor (for REL); or number of sites under pervasive diversifying selection at 0.9 posterior probability (FUBAR); j: Number of negatively selected sites at 0.05 significance (for SLAC, FEL) or 50 Bayes factor (for REL); or number of sites under pervasive purifying selection at 0.9 posterior probability (FUBAR); ω: mean dN/dS.