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. 2009 Nov 9;106(48):20186–20191. doi: 10.1073/pnas.0812076106

Table 1.

RNA-binding analyses of FBF-2

RNA RNA sequence* Kd (nM) Krel
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gld-1 FBEa UGUGCCAUA 33.2 ± 1.5 1.0
gld-1 FBEa G4A UGUACCAUA 39.4 ± 1.3 1.2
FBE UGUACUAUA 45.8 ± 3.2 1.4
fem-3 PME UGUGUCAUU 52.9 ± 2.4 1.6
PME_U9A UGUGUCAUA 56.7 ± 3.4 1.7
PME_U9C UGUGUCAUC 81.3 ± 3.5 2.4
ced-4 FBEa UGUACAAUA 73.6 ± 1.7 2.2
mpk-1 FBEb UGUAAUAUA 81.7 ± 2.8 2.5
fog-1 FBEa UGUAAAAUC 96.9 ± 3.4 2.9
gld-1 FBEb UGUGUUAUC 127 ± 6.4 3.8
NRE UGUAUAUA >1,000§ >30

*Numbers indicate positions in the core recognition sequence. Bases that differ from the sequence of gld-1 FBEa are shown in boldface.

Krel reports the affinity of FBF-2 for the RNA sequence relative to the affinity of FBF-2 for gld-1 FBEa RNA. Double daggers () denote statistically significant differences (P < 0.05).

§Saturable binding could not be achieved at the highest protein concentration; therefore, we report a lower limit for the Kd.