Structure
atLeast majority ProS Experiment
:order disorder conflict PDB cluster ProS Pfam Domain SEG
474
order/disorder by at least rule
disorder by at least rule
order/disorder by majority rule
Seq 1-323 Hetero dimer : IID00262 Complex
Region 3vrp A 1-11 disorder
Region 3vrp A 12-34 order
Region 3vrp A 35-38 disorder
Region 3vrp A 39-100 order
Region 3vrp A 101-114 disorder
Region 3vrp A 115-320 order
Region 3vrp A 321-323 disorder
Region 3vrr A 1-12 disorder
Region 3vrr A 13-34 order
Region 3vrr A 35-38 disorder
Region 3vrr A 39-64 order
Region 3vrr A 65-67 disorder
Region 3vrr A 68-101 order
Region 3vrr A 102-108 disorder
Region 3vrr A 109-317 order
Region 3vrr A 318-323 disorder
Seq 1-323 Hetero dimer : IID00708 Complex
Region 3vro A 1-12 disorder
Region 3vro A 13-33 order
Region 3vro A 34-38 disorder
Region 3vro A 39-64 order
Region 3vro A 65-67 disorder
Region 3vro A 68-98 order
Region 3vro A 99-114 disorder
Region 3vro A 115-320 order
Region 3vro A 321-323 disorder
Region 3vrn A 1-11 disorder
Region 3vrn A 12-33 order
Region 3vrn A 34-38 disorder
Region 3vrn A 39-100 order
Region 3vrn A 101-114 disorder
Region 3vrn A 115-320 order
Region 3vrn A 321-323 disorder
Region 3vrq A 1-10 disorder
Region 3vrq A 11-32 order
Region 3vrq A 33-40 disorder
Region 3vrq A 41-62 order
Region 3vrq A 63-69 disorder
Region 3vrq A 70-97 order
Region 3vrq A 98-114 disorder
Region 3vrq A 115-320 order
Region 3vrq A 321-323 disorder
Region 3vrq B 1-11 disorder
Region 3vrq B 12-33 order
Region 3vrq B 34-39 disorder
Region 3vrq B 40-64 order
Region 3vrq B 65-69 disorder
Region 3vrq B 70-97 order
Region 3vrq B 98-115 disorder
Region 3vrq B 116-184 order
Region 3vrq B 185-189 disorder
Region 3vrq B 190-320 order
Region 3vrq B 321-323 disorder
Seq 9-323 Hetero tetramer : IID00262 Complex
Region 3op0 A 9-9 disorder
Region 3op0 A 10-323 order
Region 3op0 B 9-9 disorder
Region 3op0 B 10-323 order
341-341 Phosphotyrosine; by SRC
Prediction
Disorder 1-10,317-345,407-474
ProS 317-345,407-412,419-443
Disorder 1-10,39-39,66-71,324-328,402-474
Order 11-38,40-65,72-323,329-401
Function
Function in SwissProt
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. Functionally coupled with the E2 ubiquitin-protein ligases UB2D1, UB2D2 and UB2D3. Regulator of EGFR mediated signal transduction; upon EGF activation, ubiquitinates EGFR. Isoform 1, but not isoform 2, inhibits EGF stimulated MAPK1 activation. Promotes ubiquitination of SRC phosphorylated at 'Tyr-419'. In collaboration with CD2AP may act as regulatory checkpoint for Ret signaling by modulating the rate of RET degradation after ligand activation; CD2AP converts it from an inhibitor to a promoter of RET degradation; the function limits the potency of GDNF on neuronal survival.
Biological Process
See also
Diagram with PDB data
EGFR/CBL Crystal structure of c-Cbl-TKB domain complexed with its binding motif in EGF receptor'
CFTR/GOPC PDZ Domain of CAL (Cystic Fibrosis Transmembrane Regulator-Associated Ligand)