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. 2009 Oct 6;4(10):e7290. doi: 10.1371/journal.pone.0007290

Table 1. Base substitution specificity of allelic variant W438 of human Polλ during short gap filling synthesis.

Enzyme Mispair # mutantsc E.R.d×10−4
Polλ R438 a T • dGTP 6 2.5
T • dCTP 0 ≤0.4
T • dTTP 0 ≤0.4
G • dATP 0 ≤0.4
G • dGTP 0 ≤0.4
A • dCTP 31 13
A • dGTP 1 0.4
A • dATP 1 0.4
Polλ W438 b T • dGTP 26 10
T • dCTP 0 ≤0.4
T • dTTP 0 ≤0.4
G • dATP 9 3.5
G • dGTP 0 ≤0.4
A • dCTP 57 22
A • dGTP 3 1.2
A • dATP 0 ≤0.4
a

Mutation Frequency (Polλ R438): 9.8×10−4.

b

Mutation Frequency (Polλ W438): 22.05×10−4.

c

Total sequenced: Polλ R438->42; Polλ W438->96.

d

The error rates are calculated based on sequencing mutants from two different reactions with each enzyme, and using the average mutant frequency for those two experiments, i.e., 9.8×10−4 and 22.05×10−4 for Polλ R438 and Polλ W438, respectively.