Protein detail

STYK1

Tyrosine-protein kinase STYK1 (EC 2.7.10.2) (Novel oncogene with kinase domain) (Protein PK-unique) (Serine/threonine/tyrosine kinase 1)

Entry name
STYK1
UniProt ID
EVMP confidence score
0.28
Supporting publications (n)
2
Transmembrane count
1
Protein classification
EnzymesPredicted intracellular proteinsPredicted membrane proteins
Basic Information
Protein Names
Tyrosine-protein kinase STYK1 (EC 2.7.10.2) (Novel oncogene with kinase domain) (Protein PK-unique) (Serine/threonine/tyrosine kinase 1)
Protein Class (3)
EnzymesPredicted intracellular proteinsPredicted membrane proteins
Protein Function (4)
  • ENZYME proteins:Transferases
  • Enzymes
  • Kinases:Tyr protein kinases
  • Predicted intracellular proteins
Transmembrane
26..46; Helical
Transmembrane Count
1
Entrez Gene Symbol
Gene Synonym (3)
DKFZp761P1010NOKSuRTK106
Gene Description
Serine/threonine/tyrosine kinase 1
Chromosome
12
Position
10618923-10674318
Supporting publications (n)
2
EVMP confidence score
0.28
Fluorescence & Localization
STYK1 fluorescence
Cell SpecificDecidual stromal cells
Function & Pathway
Relations & Evidence21

Ligand-Receptor Signaling (19)

19 records.

CategoryParentDatabaseTransmitterReceiverSecretedPlasma Membrane (Transmembrane)Plasma Membrane (Peripheral)
plasma_membrane_transmembraneplasma_membrane_transmembraneMembranomeYes
plasma_membrane_transmembraneplasma_membrane_transmembraneOmniPathYes
receptorreceptorscConnectYesYes
tyrosine_kinasereceptorHGNCYesYes
receptorreceptorHGNCYesYes
transmembranetransmembrane_predictedPhobiusYes
transmembrane_phobiustransmembrane_predictedAlmen2009Yes
transmembrane_sosuitransmembrane_predictedAlmen2009Yes
transmembrane_tmhmmtransmembrane_predictedAlmen2009Yes
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Regulatory Interaction Network (1)

1 record.

Source Protein SymbolSource UniProt IDTarget Protein SymbolTarget UniProt IDIs DirectedIs StimulationIs InhibitionDatabaseReferences
STYK1Q6J9G0BECN1Q14457YesYesPhosphoSite_norefSIGNORiPTMnetProtMapperSIGNOR_ProtMapperREACH_ProtMapperPhosphoSite_ProtMapperProtMapper:31696776SIGNOR:31696776

Isolation & Detection Technology (1)

1 record.

EV Isolation MethodDetection MethodNumber of ReferencesReferences
Differential UltracentrifugationMass spectrometryR Sequencing136633475
Sequence, Structure & Domains

Sequences

Length
422
Mass
47,577
Sequence
MGMTRMLLECSLSDKLCVIQEKQYEVIIVPTLLVTIFLILLGVILWLFIREQRTQQQRSGPQGIAPVPPPRDLSWEAGHGGNVALPLKETSVENFLGATTPALAKLQVPREQLSEVLEQICSGSCGPIFRANMNTGDPSKPKSVILKALKEPAGLHEVQDFLGRIQFHQYLGKHKNLVQLEGCCTEKLPLYMVLEDVAQGDLLSFLWTCRRDVMTMDGLLYDLTEKQVYHIGKQVLLALEFLQEKHLFHGDVAARNILMQSDLTAKLCGLGLAYEVYTRGAISSTQTIPLKWLAPERLLLRPASIRADVWSFGILLYEMVTLGAPPYPEVPPTSILEHLQRRKIMKRPSSCTHTMYSIMKSCWRWREADRPSPRELRLRLEAAIKTADDEAVLQVPELVVPELYAAVAGIRVESLFYNYSML

Domain & Motif Annotations

Domain (FT)
114..384; Protein kinase
Protein Families (2)
  • Protein kinase superfamily
  • Tyr protein kinase family
Sequence Similarities
Belongs to the protein kinase superfamily. Tyr protein kinase family.
Clinical Relevance
Disease Involvement
Proto-oncogene
Antibody (2)
Interaction Protein
ENSG00000096384
Interaction Count
1
Interaction Dataset
intact_biogrid
Supporting Publications2
PMIDTitleRelated sentences
38762017Preliminary study on the mechanism by which exosomes derived from human exfoliated deciduous teeth improve the proliferation and osteogenic inhibitory effect of glucocorticoid-induced BMSCs.In conclusion, SHED-derived exosomes partially reversed the inhibitory effects of glucocorticoids on BMSC proliferation and osteogenesis by inhibiting the expression of HGF, ITGB8 and IL7, and upregulating the expression of EFNA1. Transcriptome sequencing analysis revealed that the differentially expressed mRNAs regulated by SHED-derived exosomes were enriched mainly in signaling pathways such as the apoptosis pathway, the PI3K-Akt signaling pathway, the Hippo signaling pathway and the p53 signaling pathway.
39166055Dental pulp stem cells regenerate neural tissue in degenerative disorders and stroke rehabilitation: A scope systematic review.DPSC-derived exosomes suppressed the expression of IL-6, IL-1β, TNF-α, and TGF, key mediators of nerve tissue inflammation.