General Information of Drug Off-Target (DOT) (ID: OTXYSIIV)

DOT Name Tyrosine-protein phosphatase non-receptor type 7 (PTPN7)
Synonyms EC 3.1.3.48; Hematopoietic protein-tyrosine phosphatase; HEPTP; Protein-tyrosine phosphatase LC-PTP
Gene Name PTPN7
UniProt ID
PTN7_HUMAN
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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PDB ID
1ZC0; 2A3K; 2GP0; 2GPH; 2HVL; 2QDC; 2QDM; 2QDP; 3D42; 3D44; 3O4S; 3O4T; 3O4U
EC Number
3.1.3.48
Pfam ID
PF00102
Sequence
MVQAHGGRSRAQPLTLSLGAAMTQPPPEKTPAKKHVRLQERRGSNVALMLDVRSLGAVEP
ICSVNTPREVTLHFLRTAGHPLTRWALQRQPPSPKQLEEEFLKIPSNFVSPEDLDIPGHA
SKDRYKTILPNPQSRVCLGRAQSQEDGDYINANYIRGYDGKEKVYIATQGPMPNTVSDFW
EMVWQEEVSLIVMLTQLREGKEKCVHYWPTEEETYGPFQIRIQDMKECPEYTVRQLTIQY
QEERRSVKHILFSAWPDHQTPESAGPLLRLVAEVEESPETAAHPGPIVVHCSAGIGRTGC
FIATRIGCQQLKARGEVDILGIVCQLRLDRGGMIQTAEQYQFLHHTLALYAGQLPEEPSP
Function Protein phosphatase that acts preferentially on tyrosine-phosphorylated MAPK1. Plays a role in the regulation of T and B-lymphocyte development and signal transduction.
Tissue Specificity Expressed exclusively in thymus and spleen.
KEGG Pathway
MAPK sig.ling pathway (hsa04010 )
Reactome Pathway
Interleukin-37 signaling (R-HSA-9008059 )
Negative regulation of MAPK pathway (R-HSA-5675221 )

Molecular Interaction Atlas (MIA) of This DOT

Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DOT
1 Drug(s) Affected the Post-Translational Modifications of This DOT
Drug Name Drug ID Highest Status Interaction REF
Valproate DMCFE9I Approved Valproate increases the methylation of Tyrosine-protein phosphatase non-receptor type 7 (PTPN7). [1]
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5 Drug(s) Affected the Gene/Protein Processing of This DOT
Drug Name Drug ID Highest Status Interaction REF
Tretinoin DM49DUI Approved Tretinoin increases the expression of Tyrosine-protein phosphatase non-receptor type 7 (PTPN7). [2]
Acetaminophen DMUIE76 Approved Acetaminophen increases the expression of Tyrosine-protein phosphatase non-receptor type 7 (PTPN7). [3]
Paclitaxel DMLB81S Approved Paclitaxel increases the expression of Tyrosine-protein phosphatase non-receptor type 7 (PTPN7). [4]
Curcumin DMQPH29 Phase 3 Curcumin increases the expression of Tyrosine-protein phosphatase non-receptor type 7 (PTPN7). [5]
(+)-JQ1 DM1CZSJ Phase 1 (+)-JQ1 decreases the expression of Tyrosine-protein phosphatase non-receptor type 7 (PTPN7). [6]
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References

1 Integrative omics data analyses of repeated dose toxicity of valproic acid in vitro reveal new mechanisms of steatosis induction. Toxicology. 2018 Jan 15;393:160-170.
2 Transcriptional and Metabolic Dissection of ATRA-Induced Granulocytic Differentiation in NB4 Acute Promyelocytic Leukemia Cells. Cells. 2020 Nov 5;9(11):2423. doi: 10.3390/cells9112423.
3 Blood transcript immune signatures distinguish a subset of people with elevated serum ALT from others given acetaminophen. Clin Pharmacol Ther. 2016 Apr;99(4):432-41.
4 Proteomic analysis of anti-cancer effects by paclitaxel treatment in cervical cancer cells. Gynecol Oncol. 2005 Jul;98(1):45-53. doi: 10.1016/j.ygyno.2005.04.010.
5 Gene-expression profiling during curcumin-induced apoptosis reveals downregulation of CXCR4. Exp Hematol. 2007 Jan;35(1):84-95.
6 Inhibition of BRD4 attenuates tumor cell self-renewal and suppresses stem cell signaling in MYC driven medulloblastoma. Oncotarget. 2014 May 15;5(9):2355-71.