Id: acc1923
Group: 2sens
Protein: IGFBP-3
Gene Symbol: IGF2BP3
Protein Id: O00425
Protein Name: IF2B3_HUMAN
PTM: phosphorylation
Site: Ser
Site Sequence:
Disease Category: Cancer
Disease: Lung Cancer
Disease Subtype: NSCLC
Disease Cellline: H1299
Disease Info:
Drug: Cisplatin
Drug Info: "Cisplatin is a platinum-based chemotherapeutic agent widely used in the treatment of various malignancies, including ovarian, bladder, testicular, and non-small cell lung cancers, by forming DNA cross-links to interfere with replication and repair, thereby inhibiting cancer cell growth and proliferation."
Effect: inhibit
Effect Info: Phosphorylation of IGFBP - 3 by CK2 leads to enhanced resistance to cisplatin in human non - small cell lung cancer cell lines A549 and H1299.
Note: site unclear
Score: 5.0
Pubmed(PMID): 36766747
Sentence Index:
Sentence:

Sequence & Structure:

MNKLYIGNLSENAAPSDLESIFKDAKIPVSGPFLVKTGYAFVDCPDESWALKAIEALSGKIELHGKPIEVEHSVPKRQRIRKLQIRNIPPHLQWEVLDSLLVQYGVVESCEQVNTDSETAVVNVTYSSKDQARQALDKLNGFQLENFTLKVAYIPDEMAAQQNPLQQPRGRRGLGQRGSSRQGSPGSVSKQKPCDLPLRLLVPTQFVGAIIGKEGATIRNITKQTQSKIDVHRKENAGAAEKSITILSTPEGTSAACKSILEIMHKEAQDIKFTEEIPLKILAHNNFVGRLIGKEGRNLKKIEQDTDTKITISPLQELTLYNPERTITVKGNVETCAKAEEEIMKKIRESYENDIASMNLQAHLIPGLNLNALGLFPPTSGMPPPTSGPPSAMTPPYPQFEQSETETVHLFIPALSVGAIIGKQGQHIKQLSRFAGASIKIAPAEAPDAKVRMVIITGPPEAQFKAQGRIYGKIKEENFVSPKEEVKLEAHIRVPSFAAGRVIGKGGKTVNELQNLSSAEVVVPRDQTPDENDQVVVKITGHFYACQVAQRKIQEILTQVKQHQQQKALQSGPPQSRRK

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!

IGF2BP3-Ser184
Cancer Intensity
BRCA -1.827
COAD
HGSC -0.205
ccRCC 0.079
GBM 1.408
HNSC 0.649
LUAD -1.425
LUSC 0.638
non_ccRCC 0.748
PDAC 0.294
UCEC -0.357
IGF2BP3-Ser187
Cancer Intensity
BRCA
COAD
HGSC
ccRCC
GBM 0.707
HNSC
LUAD
LUSC -0.707
non_ccRCC
PDAC
UCEC
IGF2BP3-Ser496
Cancer Intensity
BRCA
COAD
HGSC
ccRCC
GBM 0.848
HNSC
LUAD
LUSC -1.103
non_ccRCC
PDAC
UCEC 0.255
IGF2BP3-Thr528
Cancer Intensity
BRCA 0.321
COAD
HGSC
ccRCC -1.23
GBM
HNSC -0.007
LUAD -0.568
LUSC -0.993
non_ccRCC
PDAC 1.163
UCEC 1.313

PTM-Disease Association:

source: PTMD

No data.

PTM-Drug Perturbation Response:

source: DecryptM
Protein Gene PTM Position Modified sequence Cell Drug pEC50 Regulation Experiment
O00425 IGF2BP3 P Ser481 IKEENFVS(ph)PK RPMI8226 BTZ 7.9942 up
O00425 IGF2BP3 P Ser481 IKEENFVS(ph)PK RPMI8226 BTZ 7.8395 up
O00425 IGF2BP3 P Ser517 TVNELQNLS(ph)SAEVVVPR RPMI8226 BTZ 7.7627 up
O00425 IGF2BP3 P Ser496 VPS(ph)FAAGR RPMI8226 BTZ 7.7311 up
O00425 IGF2BP3 P Ser496 VPS(ph)FAAGR RPMI8226 BTZ 7.6984 up
O00425 IGF2BP3 P Ser481 IKEENFVS(ph)PKEEVK RPMI8226 BTZ 7.6908 up
O00425 IGF2BP3 P Ser481 IKEENFVS(ph)PKEEVK RPMI8226 BTZ 7.6323 up
O00425 IGF2BP3 P Ser517 TVNELQNLS(ph)SAEVVVPR RPMI8226 BTZ 7.6019 up
O00425 IGF2BP3 P Ser518 TVNELQNLSS(ph)AEVVVPR RPMI8226 BTZ 7.6015 up
O00425 IGF2BP3 P Ser518 TVNELQNLSS(ph)AEVVVPR RPMI8226 BTZ 7.5364 up
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK RPMI8226 BTZ 8.5168 down
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK RPMI8226 BTZ 7.4524 down
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A431 Afatinib 7.7894 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A431 Afatinib 8.3457 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A431 Afatinib 6.264 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A431 Afatinib 7.9987 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A431 Dasatinib 9.27 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A431 Dasatinib 10.7001 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A431 Dasatinib 8.3005 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A431 Dasatinib 8.2427 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A431 Gefitinib 9.3407 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A431 Gefitinib 7.1576 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A431 Gefitinib 9.0069 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A431 Gefitinib 8.7072 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A431 Imatinib 6.7244 -
O00425 IGF2BP3 P Ser187 QGSPGS(ph)VSK A459 MK2206 4.4584 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A459 MK2206 7.6745 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A459 Selumetinib 7.3672 -
O00425 IGF2BP3 P Ser180;Ser184 GSS(ph)RQGS(ph)PGSVSK A549 AZD8055 7.2819 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A549 AZD8055 6.7524 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A549 Dactolisib 7.296 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A549 Dasatinib 8.276 -
O00425 IGF2BP3 P Ser180;Ser184 GSS(ph)RQGS(ph)PGSVSK A549 Dasatinib 2 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A549 MK2206 10.0932 -
O00425 IGF2BP3 P Ser180;Ser184 GSS(ph)RQGS(ph)PGSVSK A549 MK2206 6.7348 -
O00425 IGF2BP3 P Ser179;Ser184 GS(ph)SRQGS(ph)PGSVSK A549 MK2206 2.0945 -
O00425 IGF2BP3 P Ser180;Ser184 GSS(ph)RQGS(ph)PGSVSK A549 Nintedanib 8.5488 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A549 Nintedanib 5.2592 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A549 PD325901 8.5472 -
O00425 IGF2BP3 P Ser180;Ser184 GSS(ph)RQGS(ph)PGSVSK A549 PD325901 8.5004 -
O00425 IGF2BP3 P Ser180;Ser184 GSS(ph)RQGS(ph)PGSVSK A549 PD325901 7.017 -
O00425 IGF2BP3 P Ser179;Ser184 GS(ph)SRQGS(ph)PGSVSK A549 PD325901 6.6602 -
O00425 IGF2BP3 P Ser179;Ser184 GS(ph)SRQGS(ph)PGSVSK A549 PD325901 6.467 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A549 PD325901 6.257 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A549 Pictilisib 5.6232 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A549 Refametinib 6.2374 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK A549 Staursporin 5.9547 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK ARH-77 Rituximab 2.2794 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK ARH-77 Rituximab -3.5423 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK ARH-77 Rituximab -0.3022 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK ARH-77 Rituximab 1.1305 -
O00425 IGF2BP3 P Ser187 QGSPGS(ph)VSK ARH-77 Rituximab 0.9421 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK ARH-77 Rituximab -1.2389 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK ARH-77 Rituximab 0.9652 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK ARH-77 Rituximab 2.4692 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK ARH-77 Rituximab 2.0458 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK HeLa A485 10.539 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK HeLa A486 14 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK HeLa CUDC101 8.2979 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK HeLa Curcumin 5.6065 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK HeLa SAHA 8.3479 -
O00425 IGF2BP3 P Ser180;Ser184 GSS(ph)RQGS(ph)PGSVSK K562 Cytarabine 6.7557 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK K562 Cytarabine 4.9331 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK K562 Dasatinib 11.384 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK K562 Dasatinib 9.0268 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK K562 Dasatinib 9.005 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK K562 Dasatinib 9.7553 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK K562 Dasatinib 9.6881 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK K562 Dasatinib 9.7677 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK K562 Dasatinib 7.259 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK K562 Imatinib 9.4268 -
O00425 IGF2BP3 P Ser184;Ser187 QGS(ph)PGS(ph)VSK K562 Imatinib 9.2635 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK KYSE-520 SHP099 6.2559 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK PC-9 AZD4547 8.3749 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK PC-9 Gefitinib 6.5434 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK PC-9 GeftinibAZD4547-1to80 6.3489 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK PC-9 Lapatinib 7.297 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK PC-9 LapatinibAZD4547 8.4984 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK Ramos Rituximab -4.0441 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK Ramos Rituximab -0.8513 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK Ramos Rituximab 2.2151 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK Ramos Rituximab -1.7381 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK Ramos Rituximab -2.7558 -
O00425 IGF2BP3 P Ser179;Ser184 GS(ph)SRQGS(ph)PGSVSK RPMI8226 BTZ 10.2715 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK RPMI8226 BTZ 9.506 -
O00425 IGF2BP3 P Ser179;Ser184 GS(ph)SRQGS(ph)PGSVSK RPMI8226 BTZ 9.4823 -
O00425 IGF2BP3 P Ser481 IKEENFVS(ph)PK RPMI8226 BTZ 8.3445 -
O00425 IGF2BP3 P Ser481 IKEENFVS(ph)PK RPMI8226 BTZ 7.5974 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK RPMI8226 BTZ 4.8091 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK RPMI8226 BTZ 8.2777 -
O00425 IGF2BP3 P Ser481 IKEENFVS(ph)PK RPMI8226 BTZ 8.2537 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK RPMI8226 BTZ 8.1644 -
O00425 IGF2BP3 P Ser481 IKEENFVS(ph)PK RPMI8226 BTZ 7.8669 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK RPMI8226 BTZ 8.0595 -
O00425 IGF2BP3 P Ser517 TVNELQNLS(ph)SAEVVVPR RPMI8226 BTZ 7.8157 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK RPMI8226 BTZ 7.5665 -
O00425 IGF2BP3 P Ser517 TVNELQNLS(ph)SAEVVVPR RPMI8226 BTZ 6.6189 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK RPMI8226 BTZ 8.3678 -
O00425 IGF2BP3 P Ser517 TVNELQNLS(ph)SAEVVVPR RPMI8226 BTZ 7.6563 -
O00425 IGF2BP3 P Ser517 TVNELQNLS(ph)SAEVVVPR RPMI8226 BTZ 7.4518 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK RPMI8226 BTZ 6.8969 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK SU-DHL-4 Rituximab -1.3954 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK SU-DHL-4 Rituximab -1.2706 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK SU-DHL-4 Rituximab 0.9864 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK SU-DHL-4 Rituximab -1.4366 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK SU-DHL-4 Rituximab -0.5032 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK SU-DHL-4 Rituximab -1.4469 -
O00425 IGF2BP3 P Ser187 QGSPGS(ph)VSK SU-DHL-4 Rituximab -1.3056 -
O00425 IGF2BP3 P Ser184 QGS(ph)PGSVSK SU-DHL-4 Rituximab -1.1865 -

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: