+ |
FNTA | up-regulates activity
|
MRAS |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-242553 |
|
|
Homo sapiens |
|
pmid |
sentence |
24294527 |
Major investments have been made to target Ras through indirect routes. Inhibition of farnesyl transferase to block Ras maturation has failed in large clinical trials. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
FNTA | up-regulates activity
|
KRAS |
0.39 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-242559 |
|
|
Homo sapiens |
|
pmid |
sentence |
24294527 |
Major investments have been made to target Ras through indirect routes. Inhibition of farnesyl transferase to block Ras maturation has failed in large clinical trials. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
FNTA | up-regulates activity
|
HRAS |
0.423 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-242568 |
|
|
Homo sapiens |
|
pmid |
sentence |
24294527 |
Major investments have been made to target Ras through indirect routes. Inhibition of farnesyl transferase to block Ras maturation has failed in large clinical trials. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
TP53 | up-regulates quantity by expression
transcriptional regulation
|
FNTA |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-242408 |
|
|
Homo sapiens |
|
pmid |
sentence |
26469958 |
In this study, we provided evidence that p53 induces the expression of a group of enzymes of the MVA pathway including 3'-hydroxy-3'-methylglutaryl-coenzyme A reductase, MVA kinase, farnesyl diphosphate synthase and farnesyl diphosphate farnesyl transferase 1, in the human glioblastoma multiforme cell line, U343 cells, and in normal human astrocytes, NHAs. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
tipifarnib | down-regulates activity
chemical inhibition
|
FNTA |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-262033 |
|
|
Homo sapiens |
|
pmid |
sentence |
11196150 |
In vitro, using isolated human farnesyl protein transferase, R115777 competitively inhibited the farnesylation of lamin B and K-RasB peptide substrates, with IC50s of 0.86 nM and 7.9 nM, respectively. In a panel of 53 human tumor cell lines tested for growth inhibition, approximately 75% were found to be sensitive to R115777. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |