MATK


Summary: The protein encoded by this gene has amino acid sequence similarity to Csk tyrosine kinase and has the structural features of the CSK subfamily: SRC homology SH2 and SH3 domains, a catalytic domain, a unique N terminus, lack of myristylation signals, lack of a negative regulatory phosphorylation site, and lack of an autophosphorylation site. This protein is thought to play a significant role in the signal transduction of hematopoietic cells. It is able to phosphorylate and inactivate Src family kinases, and may play an inhibitory role in the control of T-cell proliferation. This protein might be involved in signaling in some cases of breast cancer. Three alternatively spliced transcript variants that encode different isoforms have been described for this gene. [provided by RefSeq, Jul 2008].

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Name
OMIM ID
Ensembl ID
HGNC ID
PHARMGKB ID
Map Location

GO terms in MATK


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Term Type
Evidence Type
GO Term ID
GO Des.
MF TAS GO:0004713 protein tyrosine kinase activity
MF IBA GO:0004715 non-membrane spanning protein tyrosine kinase activity
MF IBA GO:0005102 signaling receptor binding
MF IPI GO:0005515 protein binding
MF IEA GO:0005524 ATP binding
BP TAS GO:0006468 protein phosphorylation
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Gene expression in normal tissue: MATK

Gene-model tissue-cancer distribution: Bubble Plot

Gene-drug pathway distribution

Pathways in MATK


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Database
Pathway ID
Pathway Des.
reactome R-HSA-1227986 Signaling by ERBB2
reactome R-HSA-162582 Signal Transduction
reactome R-HSA-8863795 Downregulation of ERBB2 signaling
reactome R-HSA-9006934 Signaling by Receptor Tyrosine Kinases
pid kitpathway Signaling events mediated by Stem cell factor receptor (c-Kit)
pid trkrpathway Neurotrophic factor-mediated Trk receptor signaling
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Gene-Drug: Aster Plot


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Drug ID
Drug Name
Model Num.
iGMDRD280 CYTOCHALASIN B 3
iGMDRD634 SCHEMBL2608041 3
iGMDRD71 Sparfosic acid 3
iGMDRD341 Triacsin c 3
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in MATK

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Model
Level
Reference ID
Tissue
Cancer
Drug
Clinical Response
Source
No matching records found

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