1                          T-cadherin could be ADP-ribosylated by a transferase that was also present i

2 osphorylation but that arginine 33, which is ADP-ribosylated by an endogenous ADP-ribosyltransferase,

3                   However, rather than being ADP-ribosylated by an H. pylori toxin, the intrinsic pol

4      Thus, arginines 14 and 24, which can be ADP ribosylated by ART1, are critical to the regulation

5 ecular mass 80-110 kDa were more extensively ADP-ribosylated by ART1-Pro257 than ART1-Leu257, in acco

6 onding to Glu156 of Arabidopsis RIN4 are not ADP-ribosylated by bacterial AvrRpm2Psa.

7 s ADP-ribosylation comigrated with a protein ADP-ribosylated by cholera toxin and was recognized and

8   R140Q dinitrogenase reductase could not be ADP-ribosylated by DRAT, although it still formed a cros

9  subunit of cGMP phosphodiesterase (PDE), is ADP-ribosylated by endogenous ADP-ribosyltransferase whe

10 th arginine 33 and arginine 36 are similarly ADP-ribosylated by endogenous ADP-ribosyltransferase, bu

11 mber of the Ras GTPase subfamily that can be ADP ribosylated by ExoS and indicates that ExoS can inhi

12                           The 27-kDa protein ADP-ribosylated by ExoS was determined to be apolipoprot

13 haracterized the mammalian proteins that are ADP-ribosylated by ExoT, using two-dimensional SDS-PAGE

14 vity of ADP-ribosylhydrolases on RNA species ADP-ribosylated by mammalian and bacterial ARTs.

15          Several mammalian cell proteins are ADP-ribosylated by MYPE9110, and the full-length recombi

16 at transcription factor NFAT binds to and is ADP-ribosylated by PARP-1 in an activation-dependent man

17 A-PK, and the catalytic subunit of DNA-PK is ADP-ribosylated by PARP.

18 ced and TOP2-DPCs are adenosine diphosphate (ADP) ribosylated by poly(ADP-ribose) polymerase 1 (PARP1

19  HT-29 human epithelial cells, where Rac1 is ADP-ribosylated by TTS-ExoS, Rac1 was activated and relo