SMURF1
E3 ubiquitin-protein ligase SMURF1
Also known as: KIAA1625, SMUF1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9HCE7
- Gene
- SMURF1
- Ensembl
- ENSG00000198742
- Chromosome
- 7
- Canonical length
- 757 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles
OverviewNCBI Gene
This gene encodes a ubiquitin ligase that is specific for receptor-regulated SMAD proteins in the bone morphogenetic protein (BMP) pathway. This protein plays a key roll in the regulation of cell motility, cell signalling, and cell polarity. Alternative splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Dec 2010]
Canonical amino-acid sequenceUniProt
757 residues, UniProt reviewed canonical sequence.
>Q9HCE7|SMURF1
1 MSNPGTRRNG SSIKIRLTVL CAKNLAKKDF FRLPDPFAKI VVDGSGQCHS TDTVKNTLDP
61 KWNQHYDLYV GKTDSITISV WNHKKIHKKQ GAGFLGCVRL LSNAISRLKD TGYQRLDLCK
121 LNPSDTDAVR GQIVVSLQTR DRIGTGGSVV DCRGLLENEG TVYEDSGPGR PLSCFMEEPA
181 PYTDSTGAAA GGGNCRFVES PSQDQRLQAQ RLRNPDVRGS LQTPQNRPHG HQSPELPEGY
241 EQRTTVQGQV YFLHTQTGVS TWHDPRIPSP SGTIPGGDAA FLYEFLLQGH TSEPRDLNSV
301 NCDELGPLPP GWEVRSTVSG RIYFVDHNNR TTQFTDPRLH HIMNHQCQLK EPSQPLPLPS
361 EGSLEDEELP AQRYERDLVQ KLKVLRHELS LQQPQAGHCR IEVSREEIFE ESYRQIMKMR
421 PKDLKKRLMV KFRGEEGLDY GGVAREWLYL LCHEMLNPYY GLFQYSTDNI YMLQINPDSS
481 INPDHLSYFH FVGRIMGLAV FHGHYINGGF TVPFYKQLLG KPIQLSDLES VDPELHKSLV
541 WILENDITPV LDHTFCVEHN AFGRILQHEL KPNGRNVPVT EENKKEYVRL YVNWRFMRGI
601 EAQFLALQKG FNELIPQHLL KPFDQKELEL IIGGLDKIDL NDWKSNTRLK HCVADSNIVR
661 WFWQAVETFD EERRARLLQF VTGSTRVPLQ GFKALQGSTG AAGPRLFTIH LIDANTDNLP
721 KAHTCFNRID IPPYESYEKL YEKLLTAVEE TCGFAVELocalizationUniProt · AlphaFold · HPA
Whether an antibody against SMURF1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.37
- Highest tissue expression
- 34 nTPM
Expression across tissuesHPA
Tissue
- blood vessel: 34 nTPM
- esophagus: 21 nTPM
- testis: 19 nTPM
- ovary: 19 nTPM
- skin: 19 nTPM
- lung: 17 nTPM
Single-cell type
- renal collecting duct intercalated cells: 472 nCPM
- microglia: 254 nCPM
- oligodendrocytes: 249 nCPM
- urothelial cells: 233 nCPM
- papillary tip epithelial cells: 202 nCPM
- esophageal apical cells: 185 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- white matter: 6.5 nTPM
- medulla oblongata: 5.6 nTPM
- cerebral cortex: 5.3 nTPM
- pons: 5 nTPM
- hippocampal formation: 4.7 nTPM
- choroid plexus: 4.5 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.36
- gnomAD pLI
- 0.61
- gnomAD missense Z
- 2.76
- DepMap mean gene effect
- -0.11
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 9% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- BMP signaling pathway
- cell differentiation
- ectoderm development
- negative regulation of activin receptor signaling pathway
- negative regulation of BMP signaling pathway
- negative regulation of transforming growth factor beta receptor signaling pathway
- positive regulation of axon extension
- positive regulation of dendrite extension
- positive regulation of ubiquitin-dependent protein catabolic process
- proteasome-mediated ubiquitin-dependent protein catabolic process
- protein export from nucleus
- protein localization to plasma membrane
- protein polyubiquitination
- protein targeting to vacuole involved in autophagy
- receptor catabolic process
- substrate localization to autophagosome
- ubiquitin-dependent protein catabolic process
- Wnt signaling pathway, planar cell polarity pathway
- engulfment of target by autophagosome
Molecular functions
- activin receptor binding
- I-SMAD binding
- phospholipid binding
- R-SMAD binding
- SMAD binding
- transforming growth factor beta receptor binding
- ubiquitin protein ligase activity
- ubiquitin-protein transferase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SMURF1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SMURF1 as an antibody target. Whether an autoantibody or antibody against SMURF1 could matter depends on whether native SMURF1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SMURF1 is annotated at the cell surface, where native SMURF1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label SMURF1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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