Odai O, Hiroaki H, Sakata T, Tanaka T, Uesugi S
Faculty of Pharmaceutical Sciences, Osaka University, Japan.
FEBS Lett. 1990 Jul 2;267(1):150-2. doi: 10.1016/0014-5793(90)80311-6.
We have designed a hammerhead-type RNA system which consists of three RNA fragments for normal and modified complexes which contain a non-cleavable substrate with 2'-O-methylcytidine and a guanosine-to-inosine replaced enzyme. Examination of the RNA-cleaving activity and conformational properties of the complexes suggests that the 2-amino group of a conserved guanosine residue in the loop region plays an important role for maintaining both the activity and loop conformation.