Id: acc2173
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: camptothecin
Drug Info: "Camptothecin is a naturally occurring alkaloid derived from the Chinese tree Camptotheca acuminata, which functions as a topoisomerase I inhibitor, disrupting DNA replication and exhibiting antitumor activity in various cancers, including colorectal, ovarian, and lung cancers."
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: