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. 1998 Feb;42(2):447–452. doi: 10.1128/aac.42.2.447

TABLE 1.

RNA-dependent DNA polymerase activities of the mutant heterodimersa

Heterodimerb Activity (%)
Wild type 100
G190A 170
G190S 120
G190E 20
L74V-G190E 100
V75I-G190E 105
L74V 100
V75I 100
a

Individual mutations were prepared in RT(66) clones (13, 17) by the method of BspMI cassette mutagenesis as previously described (2, 3). p66-p51 heterodimers were generated and purified as previously described (4). The polymerase assays were done as previously described (4). The reactions used equal amounts of purified p66-p51 heterodimers (2.0 ng) and poly(rC) · oligo(dG) as the substrate. The amount of labeled polymer collected for the wild-type heterodimer was considered 100% activity, and the amounts of labeled polymer collected for the various mutant heterodimers were normalized to this value. 

b

The heterodimers other than the wild type are designated by the mutations they carry.