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1 ng activity in vitro towards the Ras-related Rap1 protein.
2 cently shown to exhibit exchange activity on Rap1 proteins.
3 to the chromosome terminus by telomere-bound Rap1 protein and its binding partners, Rif1p and Rif2p,
8 accepted that a normal physiological role of Rap1 proteins is to antagonize Ras mitogenic signals, pr
10 alonic acid into Rab6, but not into H-Ras or Rap1, proteins that are modified by FTase and GGTase I,
11 xamined the abilities of different truncated RAP1 proteins to perturb positioned nucleosomes via a nu
13 hibitors and expression of dominant-negative Rap1 protein, we also found that the Rap1/PKC/ERK-depend
14 Our most potent stapled peptide binds to RAP1 protein with a Ki value of 7 nM and is >100 times m
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