Tag | Content |
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CPLM ID | CPLM-005106 |
UniProt Accession | |
Genbank Protein ID | |
Genbank Nucleotide ID | |
Protein Name | E3 ubiquitin-protein ligase CBL |
Protein Synonyms/Alias | Casitas B-lineage lymphoma proto-oncogene; Proto-oncogene c-Cbl; Signal transduction protein CBL |
Gene Name | Cbl |
Gene Synonyms/Alias | |
Created Date | July 27, 2013 |
Organism | Mus musculus (Mouse) |
NCBI Taxa ID | 10090 |
Lysine Modification | Position | Peptide | Type | References |
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201 | EKTIVPWKSFRQALH | ubiquitination | [1] | 285 | RLQKFIHKPGSYIFR | acetylation | [2] | 285 | RLQKFIHKPGSYIFR | succinylation | [2] |
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Reference | [1] Proteomic analyses reveal divergent ubiquitylation site patterns in murine tissues. Wagner SA, Beli P, Weinert BT, Schölz C, Kelstrup CD, Young C, Nielsen ML, Olsen JV, Brakebusch C, Choudhary C. Mol Cell Proteomics. 2012 Dec;11(12):1578-85. [ PMID: 22790023] [2] SIRT5-Mediated Lysine Desuccinylation Impacts Diverse Metabolic Pathways. Park J, Chen Y, Tishkoff DX, Peng C, Tan M, Dai L, Xie Z, Zhang Y, Zwaans BM, Skinner ME, Lombard DB, Zhao Y. Mol Cell. 2013 Jun 27;50(6):919-30. [ PMID: 23806337] |
Functional Description | Adapter protein that functions as a negative regulator of many signaling pathways that are triggered by activation of cell surface receptors. Acts as an E3 ubiquitin-protein ligase, which accepts ubiquitin from specific E2 ubiquitin-conjugating enzymes, and then transfers it to substrates promoting their degradation by the proteasome. Recognizes activated receptor tyrosine kinases, including KIT, FLT1, FGFR1, FGFR2, PDGFRA, PDGFRB, EGFR, CSF1R, EPHA8 and KDR and terminates signaling. Recognizes membrane-bound HCK and other kinases of the SRC family and mediates their ubiquitination and degradation. Participates in signal transduction in hematopoietic cells. Plays an important role in the regulation of osteoblast differentiation and apoptosis. Essential for osteoclastic bone resorption. The Tyr-737 phosphorylated form induces the activation and recruitment of phosphatidylinositol 3-kinase to the cell membrane in a signaling pathway that is critical for osteoclast function. |
Sequence Annotation | DOMAIN 45 349 Cbl-PTB. DOMAIN 863 902 UBA. ZN_FING 379 418 RING-type. REGION 1 355 Sufficient for interaction with EPHB1. REGION 45 173 4H. REGION 174 246 EF-hand-like. REGION 247 349 SH2-like. REGION 350 378 Linker. REGION 646 913 Interaction with CD2AP (By similarity). BINDING 292 292 Phosphotyrosine (By similarity). MOD_RES 139 139 Phosphotyrosine (By similarity). MOD_RES 195 195 N6-acetyllysine (By similarity). MOD_RES 369 369 Phosphotyrosine (By similarity). MOD_RES 450 450 Phosphoserine (By similarity). MOD_RES 453 453 Phosphotyrosine (By similarity). MOD_RES 550 550 Phosphotyrosine (By similarity). MOD_RES 665 665 Phosphoserine (By similarity). MOD_RES 666 666 Phosphoserine. MOD_RES 667 667 Phosphoserine. MOD_RES 672 672 Phosphotyrosine. MOD_RES 673 673 Phosphoserine (By similarity). MOD_RES 692 692 Phosphoserine. MOD_RES 698 698 Phosphotyrosine; by ABL1. MOD_RES 737 737 Phosphotyrosine; by SRC (By similarity). MOD_RES 780 780 Phosphotyrosine (By similarity). MOD_RES 907 907 Phosphoserine (By similarity). |
Keyword | 3D-structure; Acetylation; Calcium; Cell membrane; Complete proteome; Cytoplasm; Ligase; Membrane; Metal-binding; Phosphoprotein; Polymorphism; Proto-oncogene; Reference proteome; Repeat; Ubl conjugation; Ubl conjugation pathway; Zinc; Zinc-finger. |
Sequence Source | UniProt (SWISSPROT/TrEMBL); GenBank; EMBL |
Protein Length | 913 AA |
Protein Sequence | MAGNVKKSSG AGGGGSGGSG AGGLIGLMKD AFQPHHHHHH LSPHPPCTVD KKMVEKCWKL 60 MDKVVRLCQN PKLALKNSPP YILDLLPDTY QHLRTVLSRY EGKMETLGEN EYFRVFMENL 120 MKKTKQTISL FKEGKERMYE ENSQPRRNLT KLSLIFSHML AELKGIFPSG LFQGDTFRIT 180 KADAAEFWRK AFGEKTIVPW KSFRQALHEV HPISSGLEAM ALKSTIDLTC NDYISVFEFD 240 IFTRLFQPWS SLLRNWNSLA VTHPGYMAFL TYDEVKARLQ KFIHKPGSYI FRLSCTRLGQ 300 WAIGYVTADG NILQTIPHNK PLFQALIDGF REGFYLFPDG RNQNPDLTGL CEPTPQDHIK 360 VTQEQYELYC EMGSTFQLCK ICAENDKDVK IEPCGHLMCT SCLTSWQESE GQGCPFCRCE 420 IKGTEPIVVD PFDPRGSGSL LRQGAEGAPS PNYDDDDDER ADDSLFMMKE LAGAKVERPS 480 SPFSMAPQAS LPPVPPRLDL LQQRAPVPAS TSVLGTASKA ASGSLHKDKP LPIPPTLRDL 540 PPPPPPDRPY SVGAETRPQR RPLPCTPGDC PSRDKLPPVP SSRPGDSWLS RPIPKVPVAT 600 PNPGDPWNGR ELTNRHSLPF SLPSQMEPRA DVPRLGSTFS LDTSMTMNSS PVAGPESEHP 660 KIKPSSSANA IYSLAARPLP MPKLPPGEQG ESEEDTEYMT PTSRPVGVQK PEPKRPLEAT 720 QSSRACDCDQ QIDSCTYEAM YNIQSQALSV AENSASGEGN LATAHTSTGP EESENEDDGY 780 DVPKPPVPAV LARRTLSDIS NASSSFGWLS LDGDPTNFNE GSQVPERPPK PFPRRINSER 840 KASSYQQGGG ATANPVATAP SPQLSSEIER LMSQGYSYQD IQKALVIAHN NIEMAKNILR 900 EFVSISSPAH VAT 913 |
Gene Ontology | GO:0005737; C:cytoplasm; IEA:UniProtKB-SubCell. GO:0005634; C:nucleus; IEA:InterPro. GO:0005886; C:plasma membrane; IEA:UniProtKB-SubCell. GO:0005509; F:calcium ion binding; IEA:InterPro. GO:0004871; F:signal transducer activity; IEA:InterPro. GO:0004842; F:ubiquitin-protein ligase activity; IEA:InterPro. GO:0008270; F:zinc ion binding; IEA:InterPro. GO:0045453; P:bone resorption; ISS:UniProtKB. GO:0007166; P:cell surface receptor signaling pathway; IEA:InterPro. GO:0043066; P:negative regulation of apoptotic process; IEA:Compara. GO:0014068; P:positive regulation of phosphatidylinositol 3-kinase cascade; IEA:Compara. GO:0006468; P:protein phosphorylation; ISS:UniProtKB. |
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SMART | |
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PRINTS | |