Id: | acc2541 |
Group: | 2sens |
Protein: | THOC5 |
Gene Symbol: | THOC5 |
Protein Id: | Q13769 |
Protein Name: | THOC5_HUMAN |
PTM: | phosphorylation |
Site: | Tyr225 |
Site Sequence: | LKEIEVKKEYLSSLQPRLNSI |
Disease Category: | Cancer |
Disease: | Leukemia |
Disease Subtype: | CML |
Disease Cellline: | K562 |
Disease Info: | |
Drug: | nilotinib |
Drug Info: | "Nilotinib is a tyrosine kinase inhibitor used in the treatment of Philadelphia chromosome-positive chronic myeloid leukemia (CML) in both newly diagnosed and resistant or intolerant cases, specifically targeting the BCR-ABL protein to inhibit cancer cell proliferation." |
Effect: | sensitize |
Effect Info: | "The phosphorylation level of THOC7 is elevated in myeloid leukemia, and this phosphorylation is highly sensitive to drugs used in the treatment of chronic myeloid leukemia (CML)." |
Note: | |
Score: | 5.0 |
Pubmed(PMID): | 23032722 |
Sentence Index: | 23032722_4-5 |
Sentence: | We demonstrate that THOC5 phosphorylation is mediated by Src PTK and CD45 protein tyrosine phosphatase action and that this event is sensitive to oxidative status. We show that THOC5 phosphorylation is elevated in stem cells from patients with chronic myeloid leukemia (CML) and that this phosphorylation is sensitive to the frontline drugs used in CML treatment. |
Sequence & Structure:
MSSESSKKRKPKVIRSDGAPAEGKRNRSDTEQEGKYYSEEAEVDLRDPGRDYELYKYTCQELQRLMAEIQDLKSRGGKDVAIEIEERRIQSCVHFMTLKKLNRLAHIRLKKGRDQTHEAKQKVDAYHLQLQNLLYEVMHLQKEITKCLEFKSKHEEIDLVSLEEFYKEAPPDISKAEVTMGDPHQQTLARLDWELEQRKRLAEKYRECLSNKEKILKEIEVKKEYLSSLQPRLNSIMQASLPVQEYLFMPFDQAHKQYETARHLPPPLYVLFVQATAYGQACDKTLSVAIEGSVDEAKALFKPPEDSQDDESDSDAEEEQTTKRRRPTLGVQLDDKRKEMLKRHPLSVMLDLKCKDDSVLHLTFYYLMNLNIMTVKAKVTTAMELITPISAGDLLSPDSVLSCLYPGDHGKKTPNPANQYQFDKVGILTLSDYVLELGHPYLWVQKLGGLHFPKEQPQQTVIADHSLSASHMETTMKLLKTRVQSRLALHKQFASLEHGIVPVTSDCQYLFPAKVVSRLVKWVTVAHEDYMELHFTKDIVDAGLAGDTNLYYMALIERGTAKLQAAVVLNPGYSSIPPVFQLCLNWKGEKTNSNDDNIRAMEGEVNVCYKELCGPWPSHQLLTNQLQRLCVLLDVYLETESHDDSVEGPKEFPQEKMCLRLFRGPSRMKPFKYNHPQGFFSHR
Select PDB:
No data.
Protein Tractability:
source: Open TargetsPTM Intensity:
source: CPTACNo intensity data of this site,
show all other sites!
THOC5-Ser16 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | 0.302 | ||||
COAD | |||||
HGSC | |||||
ccRCC | |||||
GBM | |||||
HNSC | |||||
LUAD | -0.452 | ||||
LUSC | |||||
non_ccRCC | |||||
PDAC | -1.085 | ||||
UCEC | 1.235 |
THOC5-Ser28 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | -1.591 | ||||
COAD | -1.372 | ||||
HGSC | -0.358 | ||||
ccRCC | |||||
GBM | 0 | ||||
HNSC | 0.966 | ||||
LUAD | 0.251 | ||||
LUSC | -0.241 | ||||
non_ccRCC | 1.804 | ||||
PDAC | 0.257 | ||||
UCEC | 0.284 |
THOC5-Ser307 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | 1.147 | ||||
COAD | -0.044 | ||||
HGSC | |||||
ccRCC | 0.746 | ||||
GBM | -1.828 | ||||
HNSC | -1.118 | ||||
LUAD | 0.072 | ||||
LUSC | 0.235 | ||||
non_ccRCC | -0.966 | ||||
PDAC | 0.894 | ||||
UCEC | 0.861 |
THOC5-Ser312 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | -0.674 | ||||
COAD | -0.778 | ||||
HGSC | |||||
ccRCC | 0.683 | ||||
GBM | -1.125 | ||||
HNSC | -0.544 | ||||
LUAD | -0.722 | ||||
LUSC | -0.344 | ||||
non_ccRCC | 2.009 | ||||
PDAC | 0.507 | ||||
UCEC | 0.989 |
THOC5-Ser314 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | -0.767 | ||||
COAD | -0.981 | ||||
HGSC | |||||
ccRCC | 0.646 | ||||
GBM | -1.225 | ||||
HNSC | 0.057 | ||||
LUAD | -0.64 | ||||
LUSC | -0.431 | ||||
non_ccRCC | 1.963 | ||||
PDAC | 0.435 | ||||
UCEC | 0.943 |
THOC5-Thr328 | |
---|---|
Cancer | Intensity |
BRCA | 0.593 |
COAD | -0.13 |
HGSC | 2.591 |
ccRCC | -0.302 |
GBM | -0.255 |
HNSC | -0.06 |
LUAD | -0.005 |
LUSC | 0.156 |
non_ccRCC | -1.423 |
PDAC | -0.464 |
UCEC | -0.701 |
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
Y | 225 | U | Chronic myelogenous leukemia/chronic myeloid leukemia | Phosphorylation | 23032722 |
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: DecryptMNo data.
Function score:
source: funscoRNo data.