Aliases for UBE2L3 Gene
External Ids for UBE2L3 Gene
Previous GeneCards Identifiers for UBE2L3 Gene
The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes (E1s), ubiquitin-conjugating enzymes (E2s) and ubiquitin-protein ligases (E3s). This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. This enzyme is demonstrated to participate in the ubiquitination of p53, c-Fos, and the NF-kB precursor p105 in vitro. Several alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2009]
GeneCards Summary for UBE2L3 Gene
UBE2L3 (Ubiquitin-Conjugating Enzyme E2L 3) is a Protein Coding gene. Diseases associated with UBE2L3 include keloid formation and diffuse cutaneous systemic sclerosis. Among its related pathways are Immune System and Alpha-synuclein signaling. GO annotations related to this gene include poly(A) RNA binding and ligase activity. An important paralog of this gene is UBE2L6.
UniProtKB/Swiss-Prot for UBE2L3 Gene
Ubiquitin-conjugating enzyme E2 that specifically acts with HECT-type and RBR family E3 ubiquitin-protein ligases. Does not function with most RING-containing E3 ubiquitin-protein ligases because it lacks intrinsic E3-independent reactivity with lysine: in contrast, it has activity with the RBR family E3 enzymes, such as PARK2 and ARIH1, that function like function like RING-HECT hybrids. Accepts ubiquitin from the E1 complex and catalyzes its covalent attachment to other proteins. In vitro catalyzes Lys-11-linked polyubiquitination. Involved in the selective degradation of short-lived and abnormal proteins. Down-regulated during the S-phase it is involved in progression through the cell cycle. Regulates nuclear hormone receptors transcriptional activity. May play a role in myelopoiesis.