Table 1.
DNA | Length/bp | Sequence* | Binding affinity** |
---|---|---|---|
Ori | 67 | 5′-AAAATTTAAAAGAAGACACCAAATCAGATGCCGCCGGTCGCC GCCGGTAGGCGGGACTTCCGGTACA -3′ | ++++ |
NSBE1+2+3+4 wt | 38 | 5′- TGCCGCCGGTCGCCGCCGGTAGGCGGGACTTCCGGTACA -3 | ++++ |
NSBE1+2+3 wt | 28 | 5 - TGCCGCCGGTCGCCGCCGGTAGGCGGGAC -3′ | ++++ |
NSBE2+3+4 | 28 | 5′-AGCCGCCGGTAGGCGGGACTTTCCGGTACA-3 | + |
NSBE1-3456 | 28 | 5 - AGCTATTGGTCGCCGCCGGTAGGCGGGAC -3′ | + |
NSBE2-3456 | 28 | 5′-AGCCGCCGGTCGCTATTGGTAGGCGGGAC-3 | + |
NSBE3-3456 | 28 | 5 -AGCCGCCGGTCGCCGCCGGTAGGTAAAA C-3 | ++++ |
NSBE1+2-3456 | 28 | 5′-AGCTATTGGTCGCTATTGGTAGGCGGGAC-3′ | - |
NSBE3-1to8 | 28 | 5 - AGCCGCCGGTCGCCGCCGGTATTATTTCA -3′ | ++++ |
NSBE1+2 | 18 | 5′- TGCCGCCGGTCGCCGCCGG -3 | - |
NSBE2+3 | 18 | 5′- TGCCGCCGGTAGGCGGGAC -3′ | - |
NSBE3+4 | 18 | 5′- AGGCGGGACTTCCGGTACA -3 | - |
NSBE/19 | 19 | 5′-AGCCGCCGGTCGCCGCCGGT-3 | - |
NSBE/20 | 20 | 5 -AGCCGCCGGTCGCCGCCGGTA-3′ | - |
NSBE/21 | 21 | 5′-AGCCGCCGGTCGCCGCCGGTAG-3′ | ++ |
NSBE/23 | 23 | 5′- AGCCGCCGGTCGCCGCCGGTAGGC -3′ | +++ |
NSBE/25 | 25 | 5′- AGCCGCCGGTCGCCGCCGGTAGGCGG-3′ | ++++ |
NSBE1+2-1AA | 28 | 5′- AACCGCCGGTCACCGCCGGTAGGCGGGAC-3′ | +++ |
NSBE1+2-2TT | 28 | 5′-AGTCGCCGGTCGTCGCCGGTAGGCGGGAC-3′ | ++++ |
NSBE1+2-3TT | 28 | 5′-AGCTGCCGGTCGCTGCCGGTAGGCGGGAC-3′ | ++++ |
NSBE1+2-4AA | 28 | 5′-AGCCACCGGTCGCCACCGGTAGGCGGGAC-3′ | +++ |
NSBE1+2-5TT | 28 | 5′-AGCCGTCGGTCGCCGTCGGTAGGCGGGAC-3′ | ++++ |
NSBE1+2-6TT | 28 | 5′-AGCCGCTGGTCGCCGCTGGTAGGCGGGAC-3′ | + |
NSBE1+2-7AA | 28 | 5′-AGCCGCCAGTCGCCGCCAGTAGGCGGGAC-3′ | + |
NSBE1+2-8AA | 28 | 5′-AGCCGCCGATCGCCGCCGATAGGCGGGAC-3′ | + |
Double-stranded DNA molecules were used in EMSA, but only plus strands of those DNA molecules are listed here. All dsDNA molecules except for the Ori contain a single 5′ overhang on both strands. The bold underlined letters indicate positions of mutation. wt, wild type DNA.
The binding affinity of NS1N is shown by plus signs, and the minus sings mean no observed binding.