TEC_MOUSE - dbPTM
TEC_MOUSE - PTM Information in dbPTM
Basic Information of Protein
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
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
Experimental Post-Translational Modification Sites

* ASA = Accessible Surface Area

Locations Modification Substrate Peptides
&
Secondary Structure
ASA (%) Reference Orthologous
Protein Cluster
151PhosphorylationEKYNLFESSIRKTLP
HHHCCCHHHHHHHCC
24.5926102028
152PhosphorylationKYNLFESSIRKTLPP
HHCCCHHHHHHHCCC
21.1529176673
205PhosphorylationRLERGQEYIILEKND
CCCCCCEEEEEECCC
5.83-
227PhosphorylationDKYGSEGYIPSNYVT
CCCCCCCCCCCCCCC
12.95-
310AcetylationETATSPKKYYLAEKH
ECCCCCCCEEHHHHH
42.38-
518PhosphorylationRYVLDDQYTSSSGAK
EEEECCCCCCCCCCC
18.659473212
519PhosphorylationYVLDDQYTSSSGAKF
EEECCCCCCCCCCCC
19.2526745281
520PhosphorylationVLDDQYTSSSGAKFP
EECCCCCCCCCCCCC
19.9930635358
521PhosphorylationLDDQYTSSSGAKFPV
ECCCCCCCCCCCCCC
25.6230635358
522PhosphorylationDDQYTSSSGAKFPVK
CCCCCCCCCCCCCCC
42.4030635358
571PhosphorylationPFEKNTNYEVVTMVT
CCCCCCCCEEEEEEE
14.2022817900

Upstream regulatory proteins (kinases for phosphorylation sites, E3 ubiquitin ligases of ubiquitination sites, ...)
Modified Location Modified Residue Modification Type of Upstream Proteins Gene Name of Upstream Proteins UniProt AC of Upstream Proteins Sources
518YPhosphorylationKinaseJAK2Q62120
Uniprot
518YPhosphorylationKinaseLYNP25911
Uniprot
518YPhosphorylationKinaseTECP24604
GPS

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of TEC_MOUSE !!

Disease-associated PTM Sites based on SAP

* 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 !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
DOK1_MOUSEDok1physical
10823839
PLCG1_MOUSEPlcg1physical
10823839

Drug and Disease Associations
Kegg Drug
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of TEC_MOUSE

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Related Literatures of Post-Translational Modification
Phosphorylation
ReferencePubMed
"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.

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