SMUG1
Single-strand selective monofunctional uracil DNA glycosylase
Also known as: FDG, HMUDG, SMUG1_HUMAN, UNG3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q53HV7
- Gene
- SMUG1
- Ensembl
- ENSG00000123415
- Chromosome
- 12
- Canonical length
- 270 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli fibrillar center,Cytosol
OverviewNCBI Gene
This gene encodes a protein that participates in base excision repair by removing uracil from single- and double-stranded DNA. Many alternatively spliced transcript variants exist for this gene; the full-length nature is known for some but not all of the variants. [provided by RefSeq, Aug 2011]
Canonical amino-acid sequenceUniProt
270 residues, UniProt reviewed canonical sequence.
>Q53HV7|SMUG1
1 MPQAFLLGSI HEPAGALMEP QPCPGSLAES FLEEELRLNA ELSQLQFSEP VGIIYNPVEY
61 AWEPHRNYVT RYCQGPKEVL FLGMNPGPFG MAQTGVPFGE VSMVRDWLGI VGPVLTPPQE
121 HPKRPVLGLE CPQSEVSGAR FWGFFRNLCG QPEVFFHHCF VHNLCPLLFL APSGRNLTPA
181 ELPAKQREQL LGICDAALCR QVQLLGVRLV VGVGRLAEQR ARRALAGLMP EVQVEGLLHP
241 SPRNPQANKG WEAVAKERLN ELGLLPLLLKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SMUG1 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.27
- Highest tissue expression
- 45 nTPM
Expression across tissuesHPA
Tissue
- liver: 45 nTPM
- epididymis: 38 nTPM
- choroid plexus: 35 nTPM
- esophagus: 34 nTPM
- kidney: 32 nTPM
- stomach: 29 nTPM
Single-cell type
- esophageal apical cells: 167 nCPM
- extravillous trophoblasts: 123 nCPM
- esophageal suprabasal cells: 118 nCPM
- syncytiotrophoblasts: 115 nCPM
- migrating cytotrophoblasts: 110 nCPM
- cytotrophoblasts: 107 nCPM
Immune cell
- basophil: 90 nTPM
- eosinophil: 57 nTPM
- memory B-cell: 50 nTPM
- classical monocyte: 46 nTPM
- neutrophil: 46 nTPM
- plasmacytoid DC: 46 nTPM
Brain region
- white matter: 35 nTPM
- medulla oblongata: 35 nTPM
- choroid plexus: 33 nTPM
- thalamus: 33 nTPM
- spinal cord: 32 nTPM
- basal ganglia: 31 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)
- 1.08
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.86
- DepMap mean gene effect
- -0.17
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- DNA binding
- DNA N-glycosylase activity
- identical protein binding
- oxidized pyrimidine nucleobase lesion DNA N-glycosylase activity
- uracil DNA N-glycosylase activity
- single-strand selective uracil DNA N-glycosylase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Uracil-DNA glycosylase-like
- Uracil-DNA glycosylase-like domain superfamily
- Uracil DNA glycosylase superfamily
- Single-strand selective monofunctional uracil DNA glycosylase
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SMUG1 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 SMUG1 as an antibody target. Whether an autoantibody or antibody against SMUG1 could matter depends on whether native SMUG1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SMUG1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label SMUG1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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