CPLM 1.0 - Compendium of Protein Lysine Modification
TagContent
CPLM ID CPLM-011639
UniProt Accession
Genbank Protein ID
Genbank Nucleotide ID
Protein Name
 Tyrosine-protein kinase ITK/TSK 
Protein Synonyms/Alias
 Interleukin-2-inducible T-cell kinase; IL-2-inducible T-cell kinase; Kinase EMT; T-cell-specific kinase; Tyrosine-protein kinase Lyk 
Gene Name
 ITK 
Gene Synonyms/Alias
 EMT; LYK 
Created Date
 July 27, 2013 
Organism
 Homo sapiens (Human) 
NCBI Taxa ID
 9606 
Lysine Modification
Position
Peptide
Type
References
13LLEEQLIKKSQQKRRubiquitination[1]
14LEEQLIKKSQQKRRTubiquitination[2]
52HGKKRTLKGSIELSRubiquitination[2]
61SIELSRIKCVEIVKSubiquitination[2]
107QRWVLALKEETRNNNubiquitination[2, 3]
119NNNSLVPKYHPNFWMubiquitination[2, 3]
129PNFWMDGKWRCCSQLubiquitination[1, 2]
138RCCSQLEKLATGCAQubiquitination[1, 2]
150CAQYDPTKNASKKPLubiquitination[1, 2]
154DPTKNASKKPLPPTPubiquitination[2]
229PSSYLVEKSPNNLETubiquitination[1, 2]
242ETYEWYNKSISRDKAubiquitination[1, 2, 3]
251ISRDKAEKLLLDTGKubiquitination[1, 2]
258KLLLDTGKEGAFMVRubiquitination[1, 2, 3]
291SENNPCIKHYHIKETubiquitination[1, 2, 3]
296CIKHYHIKETNDNPKacetylation[4]
296CIKHYHIKETNDNPKubiquitination[2]
344PVCFGRQKAPVTAGLubiquitination[2]
391NKDKVAIKTIREGAMubiquitination[2, 3]
412EEAEVMMKLSHPKLVubiquitination[2]
497VGENQVIKVSDFGMTubiquitination[1, 2]
519YTSSTGTKFPVKWASubiquitination[1, 2, 3]
523TGTKFPVKWASPEVFubiquitination[1, 2]
Reference
 [1] Methods for quantification of in vivo changes in protein ubiquitination following proteasome and deubiquitinase inhibition.
 Udeshi ND, Mani DR, Eisenhaure T, Mertins P, Jaffe JD, Clauser KR, Hacohen N, Carr SA.
 Mol Cell Proteomics. 2012 May;11(5):148-59. [PMID: 22505724]
 [2] Refined preparation and use of anti-diglycine remnant (K-ε-GG) antibody enables routine quantification of 10,000s of ubiquitination sites in single proteomics experiments.
 Udeshi ND, Svinkina T, Mertins P, Kuhn E, Mani DR, Qiao JW, Carr SA.
 Mol Cell Proteomics. 2013 Mar;12(3):825-31. [PMID: 23266961]
 [3] Integrated proteomic analysis of post-translational modifications by serial enrichment.
 Mertins P, Qiao JW, Patel J, Udeshi ND, Clauser KR, Mani DR, Burgess MW, Gillette MA, Jaffe JD, Carr SA.
 Nat Methods. 2013 Jul;10(7):634-7. [PMID: 23749302]
 [4] Lysine acetylation targets protein complexes and co-regulates major cellular functions.
 Choudhary C, Kumar C, Gnad F, Nielsen ML, Rehman M, Walther TC, Olsen JV, Mann M.
 Science. 2009 Aug 14;325(5942):834-40. [PMID: 19608861
Functional Description
 Tyrosine kinase that plays an essential role in regulation of the adaptive immune response. Regulates the development, function and differentiation of conventional T-cells and nonconventional NKT-cells. When antigen presenting cells (APC) activate T-cell receptor (TCR), a series of phosphorylation lead to the recruitment of ITK to the cell membrane, in the vicinity of the stimulated TCR receptor, where it is phosphorylated by LCK. Phosphorylation leads to ITK autophosphorylation and full activation. Once activated, phosphorylates PLCG1, leading to the activation of this lipase and subsequent cleavage of its substrates. In turn, the endoplasmic reticulum releases calcium in the cytoplasm and the nuclear activator of activated T-cells (NFAT) translocates into the nucleus to perform its transcriptional duty. Phosphorylates 2 essential adapter proteins: the linker for activation of T-cells/LAT protein and LCP2. Then, a large number of signaling molecules such as VAV1 are recruited and ultimately lead to lymphokine production, T-cell proliferation and differentiation. 
Sequence Annotation
 DOMAIN 4 111 PH.
 DOMAIN 171 231 SH3.
 DOMAIN 239 338 SH2.
 DOMAIN 363 615 Protein kinase.
 ZN_FING 113 149 Btk-type.
 NP_BIND 369 377 ATP (By similarity).
 ACT_SITE 482 482 Proton acceptor (By similarity).
 METAL 121 121 Zinc (By similarity).
 METAL 132 132 Zinc (By similarity).
 METAL 133 133 Zinc (By similarity).
 METAL 143 143 Zinc (By similarity).
 BINDING 391 391 ATP (By similarity).
 MOD_RES 180 180 Phosphotyrosine; by autocatalysis.
 MOD_RES 512 512 Phosphotyrosine; by LCK.
 MOD_RES 565 565 Phosphoserine.  
Keyword
 3D-structure; Adaptive immunity; ATP-binding; Complete proteome; Cytoplasm; Direct protein sequencing; Disease mutation; Immunity; Kinase; Metal-binding; Nucleotide-binding; Phosphoprotein; Polymorphism; Reference proteome; SH2 domain; SH3 domain; Transferase; Tyrosine-protein kinase; Zinc; Zinc-finger. 
Sequence Source
 UniProt (SWISSPROT/TrEMBL); GenBank; EMBL 
Protein Length
 620 AA 
Protein Sequence
MNNFILLEEQ LIKKSQQKRR TSPSNFKVRF FVLTKASLAY FEDRHGKKRT LKGSIELSRI 60
KCVEIVKSDI SIPCHYKYPF QVVHDNYLLY VFAPDRESRQ RWVLALKEET RNNNSLVPKY 120
HPNFWMDGKW RCCSQLEKLA TGCAQYDPTK NASKKPLPPT PEDNRRPLWE PEETVVIALY 180
DYQTNDPQEL ALRRNEEYCL LDSSEIHWWR VQDRNGHEGY VPSSYLVEKS PNNLETYEWY 240
NKSISRDKAE KLLLDTGKEG AFMVRDSRTA GTYTVSVFTK AVVSENNPCI KHYHIKETND 300
NPKRYYVAEK YVFDSIPLLI NYHQHNGGGL VTRLRYPVCF GRQKAPVTAG LRYGKWVIDP 360
SELTFVQEIG SGQFGLVHLG YWLNKDKVAI KTIREGAMSE EDFIEEAEVM MKLSHPKLVQ 420
LYGVCLEQAP ICLVFEFMEH GCLSDYLRTQ RGLFAAETLL GMCLDVCEGM AYLEEACVIH 480
RDLAARNCLV GENQVIKVSD FGMTRFVLDD QYTSSTGTKF PVKWASPEVF SFSRYSSKSD 540
VWSFGVLMWE VFSEGKIPYE NRSNSEVVED ISTGFRLYKP RLASTHVYQI MNHCWKERPE 600
DRPAFSRLLR QLAEIAESGL 620 
Gene Ontology
 GO:0005829; C:cytosol; TAS:Reactome.
 GO:0005524; F:ATP binding; IEA:UniProtKB-KW.
 GO:0046872; F:metal ion binding; IEA:UniProtKB-KW.
 GO:0004715; F:non-membrane spanning protein tyrosine kinase activity; IDA:UniProtKB.
 GO:0005543; F:phospholipid binding; IEA:InterPro.
 GO:0007202; P:activation of phospholipase C activity; ISS:UniProtKB.
 GO:0002250; P:adaptive immune response; ISS:UniProtKB.
 GO:0006968; P:cellular defense response; TAS:ProtInc.
 GO:0001816; P:cytokine production; ISS:UniProtKB.
 GO:0032609; P:interferon-gamma production; IEA:Compara.
 GO:0032633; P:interleukin-4 production; IEA:Compara.
 GO:0035556; P:intracellular signal transduction; IEA:InterPro.
 GO:0001865; P:NK T cell differentiation; IEA:Compara.
 GO:0042110; P:T cell activation; TAS:UniProtKB.
 GO:0050852; P:T cell receptor signaling pathway; ISS:UniProtKB. 
Interpro
 IPR011009; Kinase-like_dom.
 IPR011993; PH_like_dom.
 IPR001849; Pleckstrin_homology.
 IPR000719; Prot_kinase_cat_dom.
 IPR017441; Protein_kinase_ATP_BS.
 IPR001245; Ser-Thr/Tyr_kinase_cat_dom.
 IPR000980; SH2.
 IPR001452; SH3_domain.
 IPR008266; Tyr_kinase_AS.
 IPR020635; Tyr_kinase_cat_dom.
 IPR001562; Znf_Btk_motif. 
Pfam
 PF00779; BTK
 PF00169; PH
 PF07714; Pkinase_Tyr
 PF00017; SH2
 PF00018; SH3_1 
SMART
 SM00107; BTK
 SM00233; PH
 SM00252; SH2
 SM00326; SH3
 SM00219; TyrKc 
PROSITE
 PS50003; PH_DOMAIN
 PS00107; PROTEIN_KINASE_ATP
 PS50011; PROTEIN_KINASE_DOM
 PS00109; PROTEIN_KINASE_TYR
 PS50001; SH2
 PS50002; SH3
 PS51113; ZF_BTK 
PRINTS
 PR00401; SH2DOMAIN.
 PR00109; TYRKINASE.