======= SMURF2 ======= == Gene Information == * **Official Symbol**: SMURF2 * **Official Name**: SMAD specific E3 ubiquitin protein ligase 2 * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=64750|64750]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q9HAU4|Q9HAU4]] * **Interactions**: [[https://thebiogrid.org/search.php?search=SMURF2&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20SMURF2|Open PubMed]] * **OMIM**: [[https://omim.org/entry/605532|Open OMIM]] == Function Summary == * **Entrez Summary**: N/A * **UniProt Summary**: E3 ubiquitin-protein ligase which accepts ubiquitin from an E2 ubiquitin-conjugating enzyme in the form of a thioester and then directly transfers the ubiquitin to targeted substrates. Interacts with SMAD1 and SMAD7 in order to trigger their ubiquitination and proteasome-dependent degradation. In addition, interaction with SMAD7 activates autocatalytic degradation, which is prevented by interaction with SCYE1. Forms a stable complex with the TGF-beta receptor-mediated phosphorylated SMAD2 and SMAD3. In this way, SMAD2 may recruit substrates, such as SNON, for ubiquitin-mediated degradation. Enhances the inhibitory activity of SMAD7 and reduces the transcriptional activity of SMAD2. Coexpression of SMURF2 with SMAD1 results in considerable decrease in steady-state level of SMAD1 protein and a smaller decrease of SMAD2 level. {ECO:0000269|PubMed:11389444, ECO:0000269|PubMed:12717440}. |C2| |WW| |HECT| |ubiquitin-dependent SMAD protein catabolic process| |positive regulation of trophoblast cell migration| |regulation of trophoblast cell migration| |transforming growth factor beta receptor binding| |negative regulation of BMP signaling pathway| |SMAD binding| |negative regulation of transforming growth factor beta receptor signaling pathway| |negative regulation of cellular response to transforming growth factor beta stimulus| |positive regulation of reproductive process| |regulation of BMP signaling pathway| |BMP signaling pathway| |Wnt signaling pathway, planar cell polarity pathway| |cellular response to BMP stimulus| |response to BMP| |ubiquitin ligase complex| |regulation of establishment of planar polarity| |regulation of transforming growth factor beta receptor signaling pathway| |regulation of cellular response to transforming growth factor beta stimulus| |negative regulation of transmembrane receptor protein serine/threonine kinase signaling pathway| |non-canonical Wnt signaling pathway| |positive regulation of canonical Wnt signaling pathway| |negative regulation of cellular response to growth factor stimulus| |regulation of reproductive process| |positive regulation of Wnt signaling pathway| |regulation of morphogenesis of an epithelium| |transmembrane receptor protein serine/threonine kinase signaling pathway| |positive regulation of protein catabolic process| |ubiquitin protein ligase activity| |membrane raft| |regulation of transmembrane receptor protein serine/threonine kinase signaling pathway| |ubiquitin-protein transferase activity| |regulation of animal organ morphogenesis| |regulation of cellular response to growth factor stimulus| |protein deubiquitination| |regulation of canonical Wnt signaling pathway| |protein modification by small protein removal| |protein polyubiquitination| |proteasome-mediated ubiquitin-dependent protein catabolic process| |proteasomal protein catabolic process| |Wnt signaling pathway| |cell-cell signaling by wnt| |regulation of Wnt signaling pathway| |regulation of protein catabolic process| |nuclear speck| |cell surface receptor signaling pathway involved in cell-cell signaling| |positive regulation of catabolic process| |cellular response to growth factor stimulus| |positive regulation of cell migration| |positive regulation of multi-organism process| |positive regulation of cell motility| |ubiquitin-dependent protein catabolic process| |response to growth factor| |modification-dependent protein catabolic process| |positive regulation of cellular component movement| |modification-dependent macromolecule catabolic process| |positive regulation of locomotion| |proteolysis involved in cellular protein catabolic process| |cellular protein catabolic process| |protein catabolic process| |protein ubiquitination| |enzyme linked receptor protein signaling pathway| |protein modification by small protein conjugation| |regulation of multi-organism process| |regulation of cell migration| |negative regulation of transcription by RNA polymerase II| |cellular macromolecule catabolic process| |regulation of cell motility| |regulation of locomotion| |protein modification by small protein conjugation or removal| |regulation of catabolic process| |regulation of cellular component movement| |macromolecule catabolic process| |regulation of anatomical structure morphogenesis| |organonitrogen compound catabolic process| |identical protein binding| |cell-cell signaling| |negative regulation of transcription, DNA-templated| |cellular response to endogenous stimulus| |negative regulation of nucleic acid-templated transcription| |negative regulation of RNA biosynthetic process| |negative regulation of signal transduction| |proteolysis| |negative regulation of RNA metabolic process| |negative regulation of cell communication| |negative regulation of signaling| |positive regulation of developmental process| |negative regulation of cellular macromolecule biosynthetic process| |negative regulation of nucleobase-containing compound metabolic process| |negative regulation of macromolecule biosynthetic process| |response to endogenous stimulus| |negative regulation of cellular biosynthetic process| |negative regulation of biosynthetic process| |negative regulation of response to stimulus| |positive regulation of signal transduction| |positive regulation of protein metabolic process| |negative regulation of gene expression| |positive regulation of multicellular organismal process| |organic substance catabolic process| |cellular catabolic process| |positive regulation of cell communication| |positive regulation of signaling| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp503|Mitomycin-C 0.06μM R08 exp503]]|-1.76| |[[:results:exp425|Beta-Estradiol 0.55μM R07 exp425]]|-1.73| |[[:results:exp94|Nocodazole 0.1μM R03 exp94]]|1.77| |[[:results:exp488|Hippuristanol 0.12μM R08 exp488]]|1.8| No correlation found to any other genes in chemogenomics. Global Fraction of Cell Lines Where Essential: 0/739 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|0/28| |bone|0/26| |breast|0/33| |central nervous system|0/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/16| |kidney|0/21| |liver|0/20| |lung|0/75| |lymphocyte|0/16| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/9| |thyroid|0/2| |upper aerodigestive|0/22| |urinary tract|0/29| |uterus|0/5| == Essentiality in NALM6 == * **Essentiality Rank**: 17230 * **Expression level (log2 read counts)**: 4.98 {{:chemogenomics:nalm6 dist.png?nolink |}}