Id: acc0810
Group: 2sens
Protein: RAF
Gene Symbol: RAF1
Protein Id: P04049
Protein Name: RAF1_HUMAN
PTM: phosphorylation
Site: Ser338
Site Sequence: KIRPRGQRDSSYYWEIEASEV
Disease Category: Cancer
Disease: Glioblastoma
Disease Subtype:
Disease Cellline: U87
Disease Info:
Drug: berberine
Drug Info: "Berberine is a bioactive alkaloid derived from plants such as *Berberis vulgaris*, with demonstrated hypoglycemic, lipid-lowering, and antimicrobial effects, primarily mediated through AMP-activated protein kinase (AMPK) activation and gut microbiota modulation."
Effect: modulate
Effect Info: "Berberine inhibits the EGFR-RAF-MEK-ERK signaling pathway by reducing the phosphorylation of RAF, MEK, and ERK, thereby inducing senescence of human glioblastoma cells."
Note:
Score: 4.0
Pubmed(PMID): 25504754
Sentence Index:
Sentence:

Sequence & Structure:

MEHIQGAWKTISNGFGFKDAVFDGSSCISPTIVQQFGYQRRASDDGKLTDPSKTSNTIRVFLPNKQRTVVNVRNGMSLHDCLMKALKVRGLQPECCAVFRLLHEHKGKKARLDWNTDAASLIGEELQVDFLDHVPLTTHNFARKTFLKLAFCDICQKFLLNGFRCQTCGYKFHEHCSTKVPTMCVDWSNIRQLLLFPNSTIGDSGVPALPSLTMRRMRESVSRMPVSSQHRYSTPHAFTFNTSSPSSEGSLSQRQRSTSTPNVHMVSTTLPVDSRMIEDAIRSHSESASPSALSSSPNNLSPTGWSQPKTPVPAQRERAPVSGTQEKNKIRPRGQRDSSYYWEIEASEVMLSTRIGSGSFGTVYKGKWHGDVAVKILKVVDPTPEQFQAFRNEVAVLRKTRHVNILLFMGYMTKDNLAIVTQWCEGSSLYKHLHVQETKFQMFQLIDIARQTAQGMDYLHAKNIIHRDMKSNNIFLHEGLTVKIGDFGLATVKSRWSGSQQVEQPTGSVLWMAPEVIRMQDNNPFSFQSDVYSYGIVLYELMTGELPYSHINNRDQIIFMVGRGYASPDLSKLYKNCPKAMKRLVADCVKKVKEERPLFPQILSSIELLQHSLPKINRSASEPSLHRAAHTEDINACTLTTSPRLPVF

Select PDB:

Known Drugs:

source: Multi-Sources

(see table)

Target Drug name MOA Phase Status Disease Source
RAF1 REGORAFENIB Serine/threonine-protein kinase RAF inhibitor 4 - neoplasm ATC
RAF1 SORAFENIB TOSYLATE Serine/threonine-protein kinase RAF inhibitor 4 - renal cell carcinoma DailyMed
RAF1 SORAFENIB TOSYLATE Serine/threonine-protein kinase RAF inhibitor 4 - thyroid carcinoma DailyMed
RAF1 REGORAFENIB Serine/threonine-protein kinase RAF inhibitor 4 - colorectal neoplasm EMA
RAF1 SORAFENIB Serine/threonine-protein kinase RAF inhibitor 3 Terminated hepatocellular carcinoma ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
RAF1 SORAFENIB Serine/threonine-protein kinase RAF inhibitor 3 Unknown status hepatocellular carcinoma ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
RAF1 SORAFENIB Serine/threonine-protein kinase RAF inhibitor 3 Recruiting hepatocellular carcinoma ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
RAF1 SORAFENIB Serine/threonine-protein kinase RAF inhibitor 3 Withdrawn hepatocellular carcinoma ClinicalTrials
RAF1 REGORAFENIB Serine/threonine-protein kinase RAF inhibitor 3 Completed hepatocellular carcinoma ClinicalTrials
RAF1 REGORAFENIB Serine/threonine-protein kinase RAF inhibitor 3 Recruiting hepatocellular carcinoma ClinicalTrials
RAF1 REGORAFENIB Serine/threonine-protein kinase RAF inhibitor 3 Terminated hepatocellular carcinoma ClinicalTrials
RAF1 SORAFENIB TOSYLATE Serine/threonine-protein kinase RAF inhibitor 3 Completed hepatocellular carcinoma ClinicalTrials
ClinicalTrials
RAF1 SORAFENIB TOSYLATE Serine/threonine-protein kinase RAF inhibitor 3 Terminated hepatocellular carcinoma ClinicalTrials
RAF1 SORAFENIB TOSYLATE Serine/threonine-protein kinase RAF inhibitor 3 Unknown status hepatocellular carcinoma ClinicalTrials
RAF1 SORAFENIB Serine/threonine-protein kinase RAF inhibitor 3 Active, not recruiting hepatocellular carcinoma ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
RAF1 SORAFENIB Serine/threonine-protein kinase RAF inhibitor 3 Completed hepatocellular carcinoma ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
ClinicalTrials
RAF1 SORAFENIB Serine/threonine-protein kinase RAF inhibitor 3 Not yet recruiting hepatocellular carcinoma ClinicalTrials
RAF1 SORAFENIB TOSYLATE Serine/threonine-protein kinase RAF inhibitor 3 Not yet recruiting hepatocellular carcinoma ClinicalTrials
RAF1 SORAFENIB TOSYLATE Serine/threonine-protein kinase RAF inhibitor 3 Active, not recruiting acute myeloid leukemia ClinicalTrials
RAF1 SORAFENIB Serine/threonine-protein kinase RAF inhibitor 3 Active, not recruiting acute myeloid leukemia ClinicalTrials
RAF1 SORAFENIB Serine/threonine-protein kinase RAF inhibitor 3 Not yet recruiting acute myeloid leukemia ClinicalTrials
RAF1 SORAFENIB Serine/threonine-protein kinase RAF inhibitor 3 Completed clear cell renal carcinoma ClinicalTrials
RAF1 SORAFENIB Serine/threonine-protein kinase RAF inhibitor 3 Completed carcinoma ClinicalTrials
ClinicalTrials
RAF1 SORAFENIB Serine/threonine-protein kinase RAF inhibitor 3 Unknown status carcinoma ClinicalTrials
RAF1 SORAFENIB TOSYLATE Serine/threonine-protein kinase RAF inhibitor 3 Completed clear cell renal carcinoma ClinicalTrials

Note: Only show clinically investigational or approved drugs with protein targets.

Protein Tractability:

source: Open Targets
Small molecule
Antibody
PROTAC
Other modalities
Approved Drug
Advanced Clinical
Phase 1 Clinical
Structure with Ligand
High-Quality Ligand
High-Quality Pocket
Med-Quality Pocket
Druggable Family
Approved Drug
Advanced Clinical
Phase 1 Clinical
UniProt loc high conf
GO CC high conf
UniProt loc med conf
UniProt SigP or TMHMM
GO CC med conf
Human Protein Atlas loc
Approved Drug
Advanced Clinical
Phase 1 Clinical
Literature
UniProt Ubiquitination
Database Ubiquitination
Half-life Data
Small Molecule Binder
Approved Drug
Advanced Clinical
Phase 1 Clinical

PTM Intensity:

source: CPTAC

No intensity data of this site,
show all other sites!

RAF1-Ser12
Cancer Intensity
BRCA 0.172
COAD
HGSC 2.108
ccRCC -0.682
GBM
HNSC
LUAD -0.189
LUSC -0.96
non_ccRCC -0.274
PDAC
UCEC -0.174
RAF1-Ser220
Cancer Intensity
BRCA
COAD
HGSC
ccRCC
GBM
HNSC 0.504
LUAD
LUSC
non_ccRCC
PDAC 0.648
UCEC -1.152
RAF1-Ser222
Cancer Intensity
BRCA
COAD -0.707
HGSC 0.707
ccRCC
GBM
HNSC
LUAD
LUSC
non_ccRCC
PDAC
UCEC
RAF1-Ser243
Cancer Intensity
BRCA
COAD
HGSC -0.637
ccRCC
GBM 1.153
HNSC -0.516
LUAD
LUSC
non_ccRCC
PDAC
UCEC
RAF1-Ser244
Cancer Intensity
BRCA
COAD
HGSC -0.707
ccRCC
GBM 0.707
HNSC
LUAD
LUSC
non_ccRCC
PDAC
UCEC
RAF1-Ser259
Cancer Intensity
BRCA
COAD -0.707
HGSC 0.707
ccRCC
GBM
HNSC
LUAD
LUSC
non_ccRCC
PDAC
UCEC
RAF1-Ser29
Cancer Intensity
BRCA -1.443
COAD 1.053
HGSC 1.395
ccRCC -0.971
GBM 0.777
HNSC 0.798
LUAD 0.392
LUSC -0.242
non_ccRCC -1.329
PDAC -0.765
UCEC 0.336
RAF1-Ser296
Cancer Intensity
BRCA
COAD -0.707
HGSC 0.707
ccRCC
GBM
HNSC
LUAD
LUSC
non_ccRCC
PDAC
UCEC
RAF1-Ser315
Cancer Intensity
BRCA
COAD
HGSC
ccRCC
GBM -0.707
HNSC
LUAD 0.707
LUSC
non_ccRCC
PDAC
UCEC
RAF1-Ser316
Cancer Intensity
BRCA
COAD
HGSC
ccRCC
GBM
HNSC 0.707
LUAD -0.707
LUSC
non_ccRCC
PDAC
UCEC
RAF1-Ser321
Cancer Intensity
BRCA 0.09
COAD
HGSC
ccRCC
GBM 0.652
HNSC -0.28
LUAD -1.608
LUSC 0.37
non_ccRCC
PDAC 1.498
UCEC -0.723
RAF1-Ser377
Cancer Intensity
BRCA 0.711
COAD
HGSC
ccRCC
GBM 0.944
HNSC
LUAD -1.519
LUSC 0.311
non_ccRCC
PDAC
UCEC -0.448
RAF1-Ser43
Cancer Intensity
BRCA -0.746
COAD -0.083
HGSC 1.675
ccRCC
GBM
HNSC
LUAD
LUSC
non_ccRCC
PDAC -0.055
UCEC -0.791
RAF1-Ser621
Cancer Intensity
BRCA
COAD -0.707
HGSC 0.707
ccRCC
GBM
HNSC
LUAD
LUSC
non_ccRCC
PDAC
UCEC
RAF1-Ser625
Cancer Intensity
BRCA
COAD
HGSC
ccRCC 0.707
GBM
HNSC -0.707
LUAD
LUSC
non_ccRCC
PDAC
UCEC
RAF1-Ser632
Cancer Intensity
BRCA
COAD
HGSC
ccRCC
GBM -0.621
HNSC 1.154
LUAD
LUSC
non_ccRCC
PDAC -0.532
UCEC
RAF1-Ser639
Cancer Intensity
BRCA
COAD
HGSC
ccRCC
GBM 0.842
HNSC 0.264
LUAD -1.105
LUSC
non_ccRCC
PDAC
UCEC
RAF1-Ser641
Cancer Intensity
BRCA 0.613
COAD
HGSC
ccRCC 0.172
GBM 0.609
HNSC -1.065
LUAD -0.714
LUSC 1.845
non_ccRCC -1.422
PDAC -0.294
UCEC 0.256
RAF1-Ser642
Cancer Intensity
BRCA
COAD -0.707
HGSC 0.707
ccRCC
GBM
HNSC
LUAD
LUSC
non_ccRCC
PDAC
UCEC
RAF1-Thr10
Cancer Intensity
BRCA
COAD
HGSC
ccRCC -1.409
GBM
HNSC 0.926
LUAD 0.099
LUSC
non_ccRCC
PDAC
UCEC 0.385
RAF1-Thr242
Cancer Intensity
BRCA
COAD
HGSC
ccRCC
GBM 0.707
HNSC -0.707
LUAD
LUSC
non_ccRCC
PDAC
UCEC
RAF1-Thr260
Cancer Intensity
BRCA
COAD 0.707
HGSC -0.707
ccRCC
GBM
HNSC
LUAD
LUSC
non_ccRCC
PDAC
UCEC
RAF1-Thr330
Cancer Intensity
BRCA
COAD
HGSC
ccRCC -0.44
GBM -1.329
HNSC 1.788
LUAD 0.033
LUSC -0.602
non_ccRCC 0.907
PDAC 0.367
UCEC -0.723
RAF1-Thr641
Cancer Intensity
BRCA
COAD -0.707
HGSC 0.707
ccRCC
GBM
HNSC
LUAD
LUSC
non_ccRCC
PDAC
UCEC

PTM-Disease Association:

source: PTMD
Residue Position State Disease Class PMID
S 338 U Alzheimer's disease Phosphorylation 17064357

State Note: Based on the distinct PTM states in diseases, PTMD classified all disease-associated PTMs into six classes, including whether the up-regulation (U) or down-regulation (D) of PTM levels, the absence (A) or presence (P) of PTMs, and the creation (C) or disruption (N) of PTM sites are associated with diseases.

PTM-Drug Perturbation Response:

source: DecryptM
Protein Gene PTM Position Modified sequence Cell Drug pEC50 Regulation Experiment
P04049 RAF1 P Ser338 GQRDS(ph)SYYWEIEASEVMLSTR K562 Dasatinib 9.8241 down
P04049 RAF1 P Ser338 GQRDS(ph)SYYWEIEASEVMLSTR K562 Dasatinib 8.8557 down
P04049 RAF1 P Ser338 GQRDS(ph)SYYWEIEASEVMLSTR BT-474 Pertuzumab -1.5377 -
P04049 RAF1 P Ser338 GQRDS(ph)SYYWEIEASEVMLSTR K562 Dasatinib 8.743 -
P04049 RAF1 P Ser338 GQRDS(ph)SYYWEIEASEVMLSTR MDA-MB-175 Pertuzumab -4.593 -
P04049 RAF1 P Ser338 GQRDS(ph)SYYWEIEASEVMLSTR MDA-MB-175 Trastuzumab -0.8503 -

pEC50 Note: pEC50 is the negative logarithm of EC50 (half-maximal effective concentration, dosage unit Mol), calculated as pEC50 = -log10(EC50), which quantifies the potency of a drug or compound.

Function score:

source: funscoR

No data.

Cross Links: