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1 tagonize the activity of regulators known as Rap proteins.
2 uction of the Phr pentapeptide inhibitors of Rap proteins.
3 that RGL2 may be an effector for Ras and/or Rap proteins.
4 n-specific kinase KinA, a novel activity for Rap proteins.
5 a target protein or regulatory peptide, the Rap protein 3-helix bundle adopts different conformation
7 wed that the endogenous C/EBPalpha, RTA, and RAP proteins all associate with RTA promoter sequences i
8 PhrLS20 peptide, which directly binds to the Rap protein and presumably induces a conformational chan
18 car gene clusters also requires a functional Rap protein, but Rap dependency can be bypassed by secon
20 ically, when complexed with target proteins, Rap proteins consist of a C-terminal tetratricopeptide r
21 at subtle differences between highly similar Rap proteins could be reflected in distinct interactions
22 igned affinity reagents, and we propose that Rap proteins could be used as scaffolds for engineering
27 d proteins encoded around the Ssp proteins ('Rap' proteins) included two specifically conferring self
29 Furthermore, upon Phr binding, the entire Rap protein is compressed along the TPR superhelical axi
31 ever, in the peptide-bound conformation, the Rap protein N-terminal 3-helix bundle and linker undergo
33 y means of crystallographic analyses how the Rap proteins of bacilli are regulated by their inhibitor
34 tein designated Cot43 that is related to the Rap proteins of Bacillus subtilis and the PlcR pleiotrop
37 mutations in a plasmid-encoded homolog of a Rap protein, RapP, caused a hyperrugose biofilm phenotyp
38 t a single residue in the switch I region of Rap proteins (residue 39) contributes considerably to th
41 activated in vitro by the direct binding of Rap proteins to a neighbouring Ras binding domain (RBD).
43 hat regulates the activity of its associated Rap protein was previously identified downstream of 8 of
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