Id: acc2171
Group: 2sens
Protein: PELP1
Gene Symbol: PELP1
Protein Id: Q8IZL8
Protein Name: PELP1_HUMAN
PTM: phosphorylation
Site: Ser1033
Site Sequence: PTLAPEALPSQGEVEREGESP
Disease Category: Cancer
Disease: Breast Cancer
Disease Subtype:
Disease Cellline: ZR75
Disease Info:
Drug: etoposide
Drug Info: "Etoposide is a chemotherapeutic agent that inhibits topoisomerase II, leading to DNA strand breaks and apoptosis, and is used in the treatment of various cancers including small cell lung cancer, testicular cancer, and lymphomas, administered intravenously or orally."
Effect: increase
Effect Info: Protein phosphorylation enhances the sensitivity to drug therapy.
Note:
Score: 5.0
Pubmed(PMID): 24786831
Sentence Index:
Sentence:

Sequence & Structure:

MAAAVLSGPSAGSAAGVPGGTGGLSAVSSGPRLRLLLLESVSGLLQPRTGSAVAPVHPPNRSAPHLPGLMCLLRLHGSVGGAQNLSALGALVSLSNARLSSIKTRFEGLCLLSLLVGESPTELFQQHCVSWLRSIQQVLQTQDPPATMELAVAVLRDLLRYAAQLPALFRDISMNHLPGLLTSLLGLRPECEQSALEGMKACMTYFPRACGSLKGKLASFFLSRVDALSPQLQQLACECYSRLPSLGAGFSQGLKHTESWEQELHSLLASLHTLLGALYEGAETAPVQNEGPGVEMLLSSEDGDAHVLLQLRQRFSGLARCLGLMLSSEFGAPVSVPVQEILDFICRTLSVSSKNISLHGDGPLRLLLLPSIHLEALDLLSALILACGSRLLRFGILIGRLLPQVLNSWSIGRDSLSPGQERPYSTVRTKVYAILELWVQVCGASAGMLQGGASGEALLTHLLSDISPPADALKLRSPRGSPDGSLQTGKPSAPKKLKLDVGEAMAPPSHRKGDSNANSDVCAAALRGLSRTILMCGPLIKEETHRRLHDLVLPLVMGVQQGEVLGSSPYTSSRCRRELYCLLLALLLAPSPRCPPPLACALQAFSLGQREDSLEVSSFCSEALVTCAALTHPRVPPLQPMGPTCPTPAPVPPPEAPSPFRAPPFHPPGPMPSVGSMPSAGPMPSAGPMPSAGPVPSARPGPPTTANHLGLSVPGLVSVPPRLLPGPENHRAGSNEDPILAPSGTPPPTIPPDETFGGRVPRPAFVHYDKEEASDVEISLESDSDDSVVIVPEGLPPLPPPPPSGATPPPIAPTGPPTASPPVPAKEEPEELPAAPGPLPPPPPPPPPVPGPVTLPPPQLVPEGTPGGGGPPALEEDLTVININSSDEEEEEEEEEEEEEEEEEEEEEDFEEEEEDEEEYFEEEEEEEEEFEEEFEEEEGELEEEEEEEDEEEEEELEEVEDLEFGTAGGEVEEGAPPPPTLPPALPPPESPPKVQPEPEPEPGLLLEVEEPGTEEERGADTAPTLAPEALPSQGEVEREGESPAAGPPPQELVEEEPSAPPTLLEEETEDGSDKVQPPPETPAEEEMETETEAEALQEKEQDDTAAMLADFIDCPPDDEKPPPPTEPDS

Select PDB:

Known Drugs:

source: Multi-Sources

(see table)

No data.

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!

PELP1-Ser1083
Cancer Intensity
BRCA 0.425
COAD 0.214
HGSC -1.918
ccRCC
GBM 1.326
HNSC
LUAD 0.017
LUSC 0.377
non_ccRCC
PDAC
UCEC -0.44
PELP1-Ser1093
Cancer Intensity
BRCA -0.614
COAD 0.447
HGSC -2.437
ccRCC
GBM 0.646
HNSC 0.519
LUAD 0.258
LUSC 0.525
non_ccRCC
PDAC 0.675
UCEC -0.019
PELP1-Ser1109
Cancer Intensity
BRCA -1.064
COAD
HGSC
ccRCC
GBM
HNSC 0.92
LUAD
LUSC
non_ccRCC
PDAC
UCEC 0.145
PELP1-Ser1123
Cancer Intensity
BRCA
COAD
HGSC
ccRCC
GBM -0.146
HNSC 0.625
LUAD -0.516
LUSC -0.848
non_ccRCC 0.377
PDAC 1.725
UCEC -1.218
PELP1-Ser527
Cancer Intensity
BRCA -0.414
COAD -1.074
HGSC
ccRCC
GBM -0.343
HNSC -0.269
LUAD -0.158
LUSC -0.99
non_ccRCC 2.19
PDAC 0.28
UCEC 0.777
PELP1-Ser531
Cancer Intensity
BRCA -0.81
COAD -0.691
HGSC 1.726
ccRCC
GBM -0.525
HNSC -0.36
LUAD -0.371
LUSC -0.911
non_ccRCC 1.866
PDAC -0.078
UCEC 0.154
PELP1-Ser535
Cancer Intensity
BRCA
COAD -1.092
HGSC
ccRCC
GBM 0.57
HNSC -0.617
LUAD -0.283
LUSC
non_ccRCC
PDAC
UCEC 1.422
PELP1-Ser708
Cancer Intensity
BRCA 2.671
COAD -0.319
HGSC -0.323
ccRCC
GBM 0.171
HNSC -0.151
LUAD -0.297
LUSC -0.321
non_ccRCC -0.562
PDAC -1.035
UCEC 0.165
PELP1-Ser793
Cancer Intensity
BRCA
COAD -0.755
HGSC -0.788
ccRCC
GBM 1.803
HNSC 0.443
LUAD -0.594
LUSC
non_ccRCC
PDAC
UCEC -0.109
PELP1-Thr1064
Cancer Intensity
BRCA
COAD
HGSC -0.707
ccRCC
GBM
HNSC
LUAD
LUSC 0.707
non_ccRCC
PDAC
UCEC
PELP1-Thr1113
Cancer Intensity
BRCA
COAD
HGSC
ccRCC
GBM 1.395
HNSC -0.18
LUAD -0.23
LUSC
non_ccRCC
PDAC
UCEC -0.985
PELP1-Thr1119
Cancer Intensity
BRCA
COAD
HGSC
ccRCC
GBM 1.087
HNSC 0.181
LUAD
LUSC -0.144
non_ccRCC 0.426
PDAC 0.316
UCEC -1.866
PELP1-Thr1132
Cancer Intensity
BRCA -2.231
COAD
HGSC
ccRCC
GBM 0.597
HNSC 0.33
LUAD
LUSC 0.056
non_ccRCC 0.264
PDAC 0.504
UCEC 0.481
PELP1-Thr1140
Cancer Intensity
BRCA 0.142
COAD
HGSC -2.448
ccRCC
GBM 0.149
HNSC 0.424
LUAD 0.481
LUSC 0.543
non_ccRCC
PDAC 0.412
UCEC 0.298
PELP1-Thr538
Cancer Intensity
BRCA
COAD
HGSC 1.142
ccRCC
GBM
HNSC -0.719
LUAD -0.423
LUSC
non_ccRCC
PDAC
UCEC
PELP1-Thr697
Cancer Intensity
BRCA 1.289
COAD -0.764
HGSC 0.06
ccRCC
GBM 1.408
HNSC 0.603
LUAD
LUSC -0.633
non_ccRCC -1.457
PDAC 0.362
UCEC -0.867
PELP1-Thr795
Cancer Intensity
BRCA -1.002
COAD -0.212
HGSC -2.334
ccRCC
GBM 0.786
HNSC 0.895
LUAD -0.114
LUSC 0.699
non_ccRCC 0.55
PDAC 0.438
UCEC 0.296

PTM-Disease Association:

source: PTMD
Residue Position State Disease Class PMID
S 1033 U Triple-negative breast cancer Phosphorylation 25788226

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
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER RPMI8226 BTZ 7.709 up
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER RPMI8226 BTZ 7.9399 up
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER RPMI8226 BTZ 7.5618 up
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER RPMI8226 BTZ 7.5743 up
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER RPMI8226 BTZ 8.3848 up
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER RPMI8226 BTZ 8.5681 up
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER HeLa Curcumin 1 up
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER HeLa CUDC101 4.261 up
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER ARH-77 Rituximab -3.6573 -
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER PC-9 LapatinibAZD4547 5.8514 -
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER K562 Dasatinib 6.2549 -
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER A459 MK2206 6.7322 -
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER A549 Tideglusib 5.7221 -
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER A549 PD325901 8.0433 -
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER A549 MK2206 7.2373 -
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER A549 Dasatinib 6.76 -
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER A549 Dasatinib 7.3458 -
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER A459 SelumetinibMK2206-3to1 6.2652 -
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER A459 SelumetinibMK2206-1to2 11.0573 -
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER A459 Selumetinib 6.5941 -
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER A459 Selumetinib 7.2756 -
Q8IZL8 PELP1 P Ser1033 GADTAPTLAPEALPS(ph)QGEVER A459 MK2206 7.5089 -

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: