| UniProt ID | TEC_MOUSE | |
|---|---|---|
| UniProt AC | P24604 | |
| Protein Name | Tyrosine-protein kinase Tec | |
| Gene Name | Tec | |
| Organism | Mus musculus (Mouse). | |
| Sequence Length | 630 | |
| Subcellular Localization |
Cytoplasm. Cell membrane Peripheral membrane protein. Cytoplasm, cytoskeleton. Following B-cell or T-cell receptors activation by antigen, translocates to the plasma membrane through its PH domain. Thrombin and integrin engagement induces translocat |
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| Protein Description | Non-receptor tyrosine kinase that contributes to signaling from many receptors and participates as a signal transducer in multiple downstream pathways, including regulation of the actin cytoskeleton. Plays a redundant role to ITK in regulation of the adaptive immune response. Regulates the development, function and differentiation of conventional T-cells and nonconventional NKT-cells. Required for TCR-dependent IL2 gene induction. Phosphorylates DOK1, one CD28-specific substrate, and contributes to CD28-signaling. Mediates signals that negatively regulate IL2RA expression induced by TCR cross-linking. Plays a redundant role to BTK in BCR-signaling for B-cell development and activation, especially by phosphorylating STAP1, a BCR-signaling protein. Required in mast cells for efficient cytokine production. Involved in both growth and differentiation mechanisms of myeloid cells through activation by the granulocyte colony-stimulating factor CSF3, a critical cytokine to promoting the growth, differentiation, and functional activation of myeloid cells. Participates in platelet signaling downstream of integrin activation. Cooperates with JAK2 through reciprocal phosphorylation to mediate cytokine-driven activation of FOS transcription. GRB10, a negative modifier of the FOS activation pathway, is another substrate of TEC. TEC is involved in G protein-coupled receptor- and integrin-mediated signalings in blood platelets. Plays a role in hepatocyte proliferation and liver regeneration and is involved in HGF-induced ERK signaling pathway. TEC regulates also FGF2 unconventional secretion (endoplasmic reticulum (ER)/Golgi-independent mechanism) under various physiological conditions through phosphorylation of FGF2 'Tyr-82'. May also be involved in the regulation of osteoclast differentiation.. | |
| Protein Sequence | MNFNTILEEILIKRSQQKKKTSLLNYKERLCVLPKSVLSYYEGRAEKKYRKGVIDISKIKCVEIVKNDDGVIPCQNKFPFQVVHDANTLYIFAPSPQSRDRWVKKLKEEIKNNNNIMIKYHPKFWADGSYQCCRQTEKLAPGCEKYNLFESSIRKTLPPAPEIKKRRPPPPIPPEEENTEEIVVAMYDFQATEAHDLRLERGQEYIILEKNDLHWWRARDKYGSEGYIPSNYVTGKKSNNLDQYEWYCRNTNRSKAEQLLRTEDKEGGFMVRDSSQPGLYTVSLYTKFGGEGSSGFRHYHIKETATSPKKYYLAEKHAFGSIPEIIEYHKHNAAGLVTRLRYPVSTKGKNAPTTAGFSYDKWEINPSELTFMRELGSGLFGVVRLGKWRAQYKVAIKAIREGAMCEEDFIEEAKVMMKLTHPKLVQLYGVCTQQKPIYIVTEFMERGCLLNFLRQRQGHFSRDMLLSMCQDVCEGMEYLERNSFIHRDLAARNCLVNEAGVVKVSDFGMARYVLDDQYTSSSGAKFPVKWCPPEVFNYSRFSSKSDVWSFGVLMWEIFTEGRMPFEKNTNYEVVTMVTRGHRLHRPKLATKYLYEVMLRCWQERPEGRPSLEDLLRTIDELVECEETFGR | |
| Overview of Protein Modification Sites with Functional and Structural Information | ||
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* ASA = Accessible Surface Area
| Locations | Modification | Substrate Peptides & Secondary Structure |
ASA (%) | Reference | Orthologous Protein Cluster |
|---|---|---|---|---|---|
| 151 | Phosphorylation | EKYNLFESSIRKTLP HHHCCCHHHHHHHCC | 24.59 | 26102028 | |
| 152 | Phosphorylation | KYNLFESSIRKTLPP HHCCCHHHHHHHCCC | 21.15 | 29176673 | |
| 205 | Phosphorylation | RLERGQEYIILEKND CCCCCCEEEEEECCC | 5.83 | - | |
| 227 | Phosphorylation | DKYGSEGYIPSNYVT CCCCCCCCCCCCCCC | 12.95 | - | |
| 310 | Acetylation | ETATSPKKYYLAEKH ECCCCCCCEEHHHHH | 42.38 | - | |
| 518 | Phosphorylation | RYVLDDQYTSSSGAK EEEECCCCCCCCCCC | 18.65 | 9473212 | |
| 519 | Phosphorylation | YVLDDQYTSSSGAKF EEECCCCCCCCCCCC | 19.25 | 26745281 | |
| 520 | Phosphorylation | VLDDQYTSSSGAKFP EECCCCCCCCCCCCC | 19.99 | 30635358 | |
| 521 | Phosphorylation | LDDQYTSSSGAKFPV ECCCCCCCCCCCCCC | 25.62 | 30635358 | |
| 522 | Phosphorylation | DDQYTSSSGAKFPVK CCCCCCCCCCCCCCC | 42.40 | 30635358 | |
| 571 | Phosphorylation | PFEKNTNYEVVTMVT CCCCCCCCEEEEEEE | 14.20 | 22817900 |
| Modified Location | Modified Residue | Modification | Function | Reference | ||
|---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of TEC_MOUSE !! | ||||||
* Distance = the distance between SAP position and PTM sites.
| Modified Location | Modification | Variant Position (Distance <= 10) |
Residue Change | SAP | Related Disease | Reference |
|---|---|---|---|---|---|---|
Oops, there are no SNP-PTM records of TEC_MOUSE !! | ||||||
| Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
|---|---|---|---|---|
| DOK1_MOUSE | Dok1 | physical | 10823839 | |
| PLCG1_MOUSE | Plcg1 | physical | 10823839 |
| Kegg Drug | ||||||
|---|---|---|---|---|---|---|
| DrugBank | ||||||
| There are no disease associations of PTM sites. | ||||||
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| Phosphorylation | |
| Reference | PubMed |
| "Quantitative time-resolved phosphoproteomic analysis of mast cellsignaling."; Cao L., Yu K., Banh C., Nguyen V., Ritz A., Raphael B.J., Kawakami Y.,Kawakami T., Salomon A.R.; J. Immunol. 179:5864-5876(2007). Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT TYR-518, AND MASSSPECTROMETRY. | |
| "Tec and Jak2 kinases cooperate to mediate cytokine-driven activationof c-fos transcription."; Yamashita Y., Watanabe S., Miyazato A., Ohya K., Ikeda U., Shimada K.,Komatsu N., Hatake K., Miura Y., Ozawa K., Mano H.; Blood 91:1496-1507(1998). Cited for: FUNCTION, PHOSPHORYLATION OF JAK2, AND PHOSPHORYLATION AT TYR-518. | |