SHFL
Shiftless antiviral inhibitor of ribosomal frameshifting protein
Also known as: C19orf66, FLJ11286, IRAV, RyDEN, SFL, SHFL_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NUL5
- Gene
- SHFL
- Ensembl
- ENSG00000130813
- Chromosome
- 19
- Canonical length
- 291 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
This gene is an interferon stimulated gene (ISG) that inhibits viral replication. The encoded protein binds nucleic acids and inhibits programmed -1 ribosomal frameshifting required for translation by many RNA viruses. Viruses inhibited by the protein include Zika virus, dengue virus and the coronaviruses, SARS-CoV and SARS-CoV2. [provided by RefSeq, Aug 2021]
Canonical amino-acid sequenceUniProt
291 residues, UniProt reviewed canonical sequence.
>Q9NUL5|SHFL
1 MSQEGVELEK SVRRLREKFH GKVSSKKAGA LMRKFGSDHT GVGRSIVYGV KQKDGQELSN
61 DLDAQDPPED MKQDRDIQAV ATSLLPLTEA NLRMFQRAQD DLIPAVDRQF ACSSCDHVWW
121 RRVPQRKEVS RCRKCRKRYE PVPADKMWGL AEFHCPKCRH NFRGWAQMGS PSPCYGCGFP
181 VYPTRILPPR WDRDPDRRST HTHSCSAADC YNRREPHVPG TSCAHPKSRK QNHLPKVLHP
241 SNPHISSGST VATCLSQGGL LEDLDNLILE DLKEEEEEEE EVEDEEGGPR ELocalizationUniProt · AlphaFold · HPA
Whether an antibody against SHFL 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)
- 0.29
- Highest tissue expression
- 101 nTPM
Expression across tissuesHPA
Tissue
- liver: 101 nTPM
- choroid plexus: 26 nTPM
- ovary: 24 nTPM
- hypothalamus: 22 nTPM
- cerebral cortex: 22 nTPM
- kidney: 21 nTPM
Single-cell type
- hepatocytes: 102 nCPM
- late spermatids: 58 nCPM
- ovarian stromal cells: 53 nCPM
- breast lactating cells: 50 nCPM
- decidual stromal cells: 49 nCPM
- t-cells: 49 nCPM
Immune cell
- NK-cell: 33 nTPM
- MAIT T-cell: 31 nTPM
- memory CD8 T-cell: 25 nTPM
- gdT-cell: 23 nTPM
- T-reg: 22 nTPM
- non-classical monocyte: 20 nTPM
Brain region
- hypothalamus: 15 nTPM
- spinal cord: 14 nTPM
- white matter: 12 nTPM
- cerebral cortex: 12 nTPM
- thalamus: 12 nTPM
- basal ganglia: 11 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)
- 0.64
- gnomAD pLI
- 0.14
- DepMap mean gene effect
- -0.12
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- defense response to virus
- innate immune response
- negative regulation of translational frameshifting
- negative regulation of viral genome replication
- regulation of translational termination
- response to interferon-beta
- response to type I interferon
- response to type II interferon
- response to type III interferon
- viral translational frameshifting
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Shiftless antiviral inhibitor of ribosomal frameshifting
- Uncharacterised protein UPF0515
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SHFL 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 SHFL as an antibody target. Whether an autoantibody or antibody against SHFL could matter depends on whether native SHFL is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SHFL 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 SHFL as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...