ライフサイエンスコーパス: geranylgeranyltransferase I

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1 re highly selective for FTase over GGTase I (geranylgeranyltransferase I).

2 tif permits this protein to be prenylated by geranylgeranyltransferase I but not II both in cell-free

3 Inhibition of geranylgeranyltransferase I by GGTi-298, but not farnesy

4 Geranylgeranyltransferase I controls the function of a v

5 he activity of FTase, but not of the related geranylgeranyltransferase I enzyme, in peripheral blood

6 This study provides evidence that geranylgeranyltransferase I (GGT) is an important signal

7 Geranylgeranyltransferase-I (GGT-I) is a heterodimeric e

8 Geranylgeranyltransferase I (GGTase I) catalyzes the tra

9 Treatment of H-Ras transgenic mice with the geranylgeranyltransferase I (GGTase I) inhibitor GGTI-21

10 f oncogenic K-Ras4B is more sensitive to the geranylgeranyltransferase I (GGTase I) inhibitor GGTI-28

11 in action on farnesyltransferase (FTase) and geranylgeranyltransferase I (GGTase I) using Chinese ham

12 erase (FTase), while modification by protein geranylgeranyltransferase I (GGTase I) was not detected.

13 ing with CIIL, a motif that is recognized by geranylgeranyltransferase I (GGTase I).

14 FTase and the closely related family member geranylgeranyltransferase I (GGTase I).

15 Protein geranylgeranyltransferase I (GGTase-I) and Rab geranylge

16 tein farnesyltransferase (FTase) and protein geranylgeranyltransferase I (GGTase-I), enzymes involved

17 tein farnesyltransferase (FTase) and protein geranylgeranyltransferase-I (GGTase-I) catalyze the pren

18 Protein geranylgeranyltransferase-I (GGTase-I) catalyzes the tra

19 we demonstrate that in human tumor cells the geranylgeranyltransferase-I (GGTase-I) inhibitor GGTI-29

20 d expression of the Rho-A prenylation enzyme geranylgeranyltransferase-I (GGTase-I).

21 is post-translationally modified by protein geranylgeranyltransferase-I (GGTase-I).

22 d) over the related prenyltransferase enzyme geranylgeranyltransferase-I (GGTase-I).

23 nt and selective peptidomimetic inhibitor of geranylgeranyltransferase I (GGTI), GGTI-2418, and its m

24 omoted the phosphorylation and activation of geranylgeranyltransferase I (GGTI-I), increased the amou

25 selective farnesyltransferase (FTI-277) and geranylgeranyltransferase-I (GGTI-298) inhibitors.

26 ) that occurs due to modification of RhoB by geranylgeranyltransferase I in drug-treated cells.

27 e have now examined the effect of insulin on geranylgeranyltransferase I in MCF-7 breast cancer cells

28 nt with tipifarnib suppressed FTase (but not geranylgeranyltransferase I) in bone marrow and peripher

29 ransformed NIH3T3 cells both FTI-276 and the geranylgeranyltransferase I inhibitor GGTI-297 are requi

30 We have recently reported that the geranylgeranyltransferase I inhibitor GGTI-298 arrests h

31 The geranylgeranyltransferase I inhibitor GGTI-298 has recen

32 ibitor of prenyltransferases, but not by the geranylgeranyltransferase I inhibitor, GGTI-298, or the

33 geranylgeranylation by the specific protein geranylgeranyltransferase-I inhibitor, GGTI-298, blocked

34 ly, we have designed farnesyltransferase and geranylgeranyltransferase I inhibitors (FTI-277 and GGTI

35 Geranylgeranyltransferase I inhibitors (GGTIs) are prese

36 Geranylgeranyltransferase I inhibitors (GGTIs) represent

37 ts farnesyltransferase inhibitors (FTIs) and geranylgeranyltransferase I inhibitors (GGTIs) upregulat

38 t known whether both farnesyltransferase and geranylgeranyltransferase I inhibitors are required for

39 Both can be prenylated by either protein geranylgeranyltransferase I (PGGT-I) or protein farnesyl

40 Protein geranylgeranyltransferase-I (PGGT-I) and protein farnesy

41 mily of peptidomimetic inhibitors of protein geranylgeranyltransferase-I (PGGTase-I) are reported.

42 ween protein farnesyltransferase and protein geranylgeranyltransferase-I. plp mutants also have alter

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