Q3TTA7
Gene name |
Cblb |
Protein name |
E3 ubiquitin-protein ligase CBL-B |
Names |
EC 2.3.2.27 , Casitas B-lineage lymphoma proto-oncogene b , RING-type E3 ubiquitin transferase CBL-B , SH3-binding protein CBL-B , Signal transduction protein CBL-B |
Species |
Mus musculus (Mouse) |
KEGG Pathway |
mmu:208650 |
EC number |
2.3.2.27: Aminoacyltransferases |
Protein Class |
|

Descriptions
Autoinhibitory domains (AIDs)
Target domain |
37-345 (TKBD) |
Relief mechanism |
PTM |
Assay |
|
Target domain |
39-343 (TKB domain) |
Relief mechanism |
PTM |
Assay |
|
Accessory elements
No accessory elements
References
- Dou H et al. (2012) "Structural basis for autoinhibition and phosphorylation-dependent activation of c-Cbl", Nature structural & molecular biology, 19, 184-92
- Wybenga-Groot LE et al. (2021) "SLAP2 Adaptor Binding Disrupts c-CBL Autoinhibition to Activate Ubiquitin Ligase Function", Journal of molecular biology, 433, 166880
- Kobashigawa Y et al. (2011) "Autoinhibition and phosphorylation-induced activation mechanisms of human cancer and autoimmune disease-related E3 protein Cbl-b", Proceedings of the National Academy of Sciences of the United States of America, 108, 20579-84
Autoinhibited structure

Activated structure

2 structures for Q3TTA7
Entry ID | Method | Resolution | Chain | Position | Source |
---|---|---|---|---|---|
5AXI | X-ray | 250 A | A/B/C | 38-343 | PDB |
AF-Q3TTA7-F1 | Predicted | AlphaFoldDB |
31 variants for Q3TTA7
Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
---|---|---|---|---|---|
rs3389387965 | 22 | I>N | No | EVA | |
rs249775570 | 142 | N>K | No | EVA | |
rs1133349872 | 143 | L>I | No | EVA | |
rs3389379518 | 213 | A>V | No | EVA | |
rs3389420469 | 224 | C>S | No | EVA | |
rs3389379593 | 406 | Q>R | No | EVA | |
rs3389410147 | 475 | N>K | No | EVA | |
rs3389410119 | 488 | Q>H | No | EVA | |
rs3389400561 | 490 | R>I | No | EVA | |
rs3389420447 | 544 | L>I | No | EVA | |
rs3389387937 | 594 | P>L | No | EVA | |
rs3389387929 | 595 | R>L | No | EVA | |
rs3406814775 | 601 | N>S | No | EVA | |
rs47774405 | 607 | R>C | No | EVA | |
rs3389400589 | 653 | V>I | No | EVA | |
rs3389417162 | 676 | V>L | No | EVA | |
rs3389422628 | 689 | L>V | No | EVA | |
rs3389436493 | 695 | E>* | No | EVA | |
rs3389334020 | 700 | T>M | No | EVA | |
rs3389379558 | 710 | I>F | No | EVA | |
rs3389436507 | 719 | N>I | No | EVA | |
rs3389410143 | 747 | G>R | No | EVA | |
rs48047742 | 748 | A>V | No | EVA | |
rs239207503 | 773 | S>F | No | EVA | |
rs3406815484 | 869 | L>F | No | EVA | |
rs3405999734 | 870 | P>S | No | EVA | |
rs3389387903 | 903 | A>V | No | EVA | |
rs3389417136 | 907 | K>* | No | EVA | |
rs3389436501 | 908 | P>S | No | EVA | |
rs3389417192 | 939 | L>P | No | EVA | |
rs3389414128 | 973 | P>L | No | EVA |
1 associated diseases with Q3TTA7
[MIM: 617799]: Intellectual developmental disorder, autosomal dominant 54 (MRD54)
A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. {ECO:0000269|PubMed:29100089, ECO:0000269|PubMed:29560374}. Note=The disease is caused by variants affecting the gene represented in this entry.
Without disease ID
- A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. {ECO:0000269|PubMed:29100089, ECO:0000269|PubMed:29560374}. Note=The disease is caused by variants affecting the gene represented in this entry.
8 regional properties for Q3TTA7
Type | Name | Position | InterPro Accession |
---|---|---|---|
repeat | Tetratricopeptide repeat 1 | 28 - 61 | IPR001440 |
domain | Calcineurin-like phosphoesterase domain, ApaH type | 236 - 428 | IPR004843 |
domain | Serine/threonine-specific protein phosphatase/bis(5-nucleosyl)-tetraphosphatase | 204 - 480 | IPR006186 |
domain | PPP domain | 136 - 228 | IPR013235 |
repeat | Tetratricopeptide repeat | 28 - 61 | IPR019734-1 |
repeat | Tetratricopeptide repeat | 62 - 95 | IPR019734-2 |
repeat | Tetratricopeptide repeat | 96 - 129 | IPR019734-3 |
domain | PP5, C-terminal metallophosphatase domain | 176 - 491 | IPR041753 |
Functions
Description | ||
---|---|---|
EC Number | 2.3.2.27 | Aminoacyltransferases |
Subcellular Localization |
|
|
PANTHER Family | ||
PANTHER Subfamily | ||
PANTHER Protein Class | ||
PANTHER Pathway Category | No pathway information available |
4 GO annotations of cellular component
Name | Definition |
---|---|
cytosol | The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes. |
membrane raft | Any of the small (10-200 nm), heterogeneous, highly dynamic, sterol- and sphingolipid-enriched membrane domains that compartmentalize cellular processes. Small rafts can sometimes be stabilized to form larger platforms through protein-protein and protein-lipid interactions. |
nucleoplasm | That part of the nuclear content other than the chromosomes or the nucleolus. |
plasma membrane | The membrane surrounding a cell that separates the cell from its external environment. It consists of a phospholipid bilayer and associated proteins. |
6 GO annotations of molecular function
Name | Definition |
---|---|
calcium ion binding | Binding to a calcium ion (Ca2+). |
phosphotyrosine residue binding | Binding to a phosphorylated tyrosine residue within a protein. |
protein kinase binding | Binding to a protein kinase, any enzyme that catalyzes the transfer of a phosphate group, usually from ATP, to a protein substrate. |
receptor tyrosine kinase binding | Binding to a receptor that possesses protein tyrosine kinase activity. |
SH3 domain binding | Binding to a SH3 domain (Src homology 3) of a protein, small protein modules containing approximately 50 amino acid residues found in a great variety of intracellular or membrane-associated proteins. |
ubiquitin protein ligase activity | Catalysis of the transfer of ubiquitin to a substrate protein via the reaction X-ubiquitin + S -> X + S-ubiquitin, where X is either an E2 or E3 enzyme, the X-ubiquitin linkage is a thioester bond, and the S-ubiquitin linkage is an amide bond |
18 GO annotations of biological process
Name | Definition |
---|---|
CD4-positive, alpha-beta T cell proliferation | The expansion of a CD4-positive, alpha-beta T cell population by cell division. |
immune response | Any immune system process that functions in the calibrated response of an organism to a potential internal or invasive threat. |
intracellular signal transduction | The process in which a signal is passed on to downstream components within the cell, which become activated themselves to further propagate the signal and finally trigger a change in the function or state of the cell. |
negative regulation of apoptotic process | Any process that stops, prevents, or reduces the frequency, rate or extent of cell death by apoptotic process. |
negative regulation of CD4-positive, alpha-beta T cell proliferation | Any process that stops, prevents or reduces the frequency, rate or extent of CD4-positive, alpha-beta T cell proliferation. |
negative regulation of T cell receptor signaling pathway | Any process that stops, prevents, or reduces the frequency, rate or extent of signaling pathways initiated by the cross-linking of an antigen receptor on a T cell. |
positive regulation of protein catabolic process | Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways resulting in the breakdown of a protein by the destruction of the native, active configuration, with or without the hydrolysis of peptide bonds. |
positive regulation of protein ubiquitination | Any process that activates or increases the frequency, rate or extent of the addition of ubiquitin groups to a protein. |
positive regulation of T cell anergy | Any process that activates or increases the frequency, rate, or extent of T cell anergy. |
protein catabolic process | The chemical reactions and pathways resulting in the breakdown of a protein by the destruction of the native, active configuration, with or without the hydrolysis of peptide bonds. |
protein ubiquitination | The process in which one or more ubiquitin groups are added to a protein. |
regulation of cell adhesion | Any process that modulates the frequency, rate or extent of attachment of a cell to another cell or to the extracellular matrix. |
regulation of platelet-derived growth factor receptor-alpha signaling pathway | Any process that modulates the frequency, rate or extent of platelet-derived growth factor receptor-alpha signaling pathway. |
regulation of T cell receptor signaling pathway | Any process that modulates the frequency, rate or extent of signaling pathways initiated by the cross-linking of an antigen receptor on a T cell. |
signal transduction | The cellular process in which a signal is conveyed to trigger a change in the activity or state of a cell. Signal transduction begins with reception of a signal (e.g. a ligand binding to a receptor or receptor activation by a stimulus such as light), or for signal transduction in the absence of ligand, signal-withdrawal or the activity of a constitutively active receptor. Signal transduction ends with regulation of a downstream cellular process, e.g. regulation of transcription or regulation of a metabolic process. Signal transduction covers signaling from receptors located on the surface of the cell and signaling via molecules located within the cell. For signaling between cells, signal transduction is restricted to events at and within the receiving cell. |
T cell activation | The change in morphology and behavior of a mature or immature T cell resulting from exposure to a mitogen, cytokine, chemokine, cellular ligand, or an antigen for which it is specific. |
T cell anergy | Any process contributing to anergy in T cells, a state of functional inactivation which is part of T cell tolerance induction. |
T cell receptor signaling pathway | The series of molecular signals initiated by the cross-linking of an antigen receptor on a T cell. |
8 homologous proteins in AiPD
UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
---|---|---|---|---|
P22681 | CBL | E3 ubiquitin-protein ligase CBL | Homo sapiens (Human) | EV |
Q9ULV8 | CBLC | E3 ubiquitin-protein ligase CBL-C | Homo sapiens (Human) | SS |
Q13191 | CBLB | E3 ubiquitin-protein ligase CBL-B | Homo sapiens (Human) | EV |
Q80XL1 | Cblc | E3 ubiquitin-protein ligase CBL-C | Mus musculus (Mouse) | SS |
P22682 | Cbl | E3 ubiquitin-protein ligase CBL | Mus musculus (Mouse) | SS |
G3V8H4 | Cblc | E3 ubiquitin-protein ligase CBL-C | Rattus norvegicus (Rat) | SS |
Q8K4S7 | Cblb | E3 ubiquitin-protein ligase CBL-B | Rattus norvegicus (Rat) | SS |
Q6DFR2 | cblb | E3 ubiquitin-protein ligase CBL-B | Xenopus tropicalis (Western clawed frog) (Silurana tropicalis) | SS |
10 | 20 | 30 | 40 | 50 | 60 |
MANSMNGRNP | GGRGGNPRKG | RILGIIDAIQ | DAVGPPKQAA | ADRRTVEKTW | KLMDKVVRLC |
70 | 80 | 90 | 100 | 110 | 120 |
QNPKLQLKNS | PPYILDILPD | TYQHLRLILS | KYDDNQKLAQ | LSENEYFKIY | IDSLMKKSKR |
130 | 140 | 150 | 160 | 170 | 180 |
AIRLFKEGKE | RMYEEQSQDR | RNLTKLSLIF | SHMLAEIKAI | FPNGQFQGDN | FRITKADAAE |
190 | 200 | 210 | 220 | 230 | 240 |
FWRKFFGDKT | IVPWKVFRQC | LHEVHQISSG | LEAMALKSTI | DLTCNDYISV | FEFDIFTRLF |
250 | 260 | 270 | 280 | 290 | 300 |
QPWGSILRNW | NFLAVTHPGY | MAFLTYDEVK | ARLQKYSTKP | GSYIFRLSCT | RLGQWAIGYV |
310 | 320 | 330 | 340 | 350 | 360 |
TGDGNILQTI | PHNKPLFQAL | IDGSREGFYL | YPDGRSYNPD | LTGLCEPTPH | DHIKVTQEQY |
370 | 380 | 390 | 400 | 410 | 420 |
ELYCEMGSTF | QLCKICAEND | KDVKIEPCGH | LMCTSCLTAW | QESDGQGCPF | CRCEIKGTEP |
430 | 440 | 450 | 460 | 470 | 480 |
IIVDPFDPRD | EGSRCCSIID | PFSIPMLDLD | DDDDREESLM | MNRLASVRKC | TDRQNSPVTS |
490 | 500 | 510 | 520 | 530 | 540 |
PGSSPLAQRR | KPQPDPLQIP | HLSLPPVPPR | LDLIQKGIVR | SPCGSPTGSP | KSSPCMVRKQ |
550 | 560 | 570 | 580 | 590 | 600 |
DKPLPAPPPP | LRDPPPPPER | PPPIPPDNRL | SRHFHHGESV | PSRDQPMPLE | AWCPRDAFGT |
610 | 620 | 630 | 640 | 650 | 660 |
NQVMGCRILG | DGSPKPGVTA | NSSLNGRHSR | MGSEQVLMRK | HRRHDLPSEG | AKVFSNGHLA |
670 | 680 | 690 | 700 | 710 | 720 |
TEEYDVPPRL | SPPPPVTTLL | PSIKCTGPLA | NCLSEKTRDT | VEDDDDEYKI | PSSHPVSLNS |
730 | 740 | 750 | 760 | 770 | 780 |
QPSHCHNVKA | PVRSCDNGHC | ILNGTHGAPS | EMKKSNIPDL | GIYLKGGGSD | SASDPVPLPP |
790 | 800 | 810 | 820 | 830 | 840 |
ARPPPRDSPK | HGSSVNRTPS | DYDLLIPPLG | EDAFDALPPS | LPPPPPPARH | SLIEHSKPPG |
850 | 860 | 870 | 880 | 890 | 900 |
SSSRPSSGQD | LFLLPSDPFF | DPTSGQVPLP | PARRAAGDSG | KANRASQDYD | QLPSSSDGSQ |
910 | 920 | 930 | 940 | 950 | 960 |
APARPPKPRP | RRTAPEIHHR | KPHGPEAALE | NVDAKIAKLM | GEGYAFEEVK | RALEIAQNNV |
970 | 980 | ||||
EVARSILREF | AFPPPVSPRL | NL |