SART1
U4/U6.U5 tri-snRNP-associated protein 1
Also known as: Ara1, HAF, SNRNP110, Snu66, SNUT1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O43290
- Gene
- SART1
- Ensembl
- ENSG00000175467
- Chromosome
- 11
- Canonical length
- 800 aa
- Protein class
- Cancer-related genes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nuclear speckles,Golgi apparatus
OverviewNCBI Gene
This gene encodes two proteins, the SART1(800) protein expressed in the nucleus of the majority of proliferating cells, and the SART1(259) protein expressed in the cytosol of epithelial cancers. The SART1(259) protein is translated by the mechanism of -1 frameshifting during posttranscriptional regulation; its full-length sequence is not published yet. The two encoded proteins are thought to be involved in the regulation of proliferation. Both proteins have tumor-rejection antigens. The SART1(259) protein possesses tumor epitopes capable of inducing HLA-A2402-restricted cytotoxic T lymphocytes in cancer patients. This SART1(259) antigen may be useful in specific immunotherapy for cancer patients and may serve as a paradigmatic tool for the diagnosis and treatment of patients with atopy. The SART1(259) protein is found to be essential for the recruitment of the tri-snRNP to the pre-spliceosome in the spliceosome assembly pathway. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
800 residues, UniProt reviewed canonical sequence.
>O43290|SART1
1 MGSSKKHRGE KEAAGTTAAA GTGGATEQPP RHREHKKHKH RSGGSGGSGG ERRKRSRERG
61 GERGSGRRGA EAEARSSTHG RERSQAEPSE RRVKREKRDD GYEAAASSKT SSGDASSLSI
121 EETNKLRAKL GLKPLEVNAI KKEAGTKEEP VTADVINPMA LRQREELREK LAAAKEKRLL
181 NQKLGKIKTL GEDDPWLDDT AAWIERSRQL QKEKDLAEKR AKLLEEMDQE FGVSTLVEEE
241 FGQRRQDLYS ARDLQGLTVE HAIDSFREGE TMILTLKDKG VLQEEEDVLV NVNLVDKERA
301 EKNVELRKKK PDYLPYAEDE SVDDLAQQKP RSILSKYDEE LEGERPHSFR LEQGGTADGL
361 RERELEEIRA KLRLQAQSLS TVGPRLASEY LTPEEMVTFK KTKRRVKKIR KKEKEVVVRA
421 DDLLPLGDQT QDGDFGSRLR GRGRRRVSEV EEEKEPVPQP LPSDDTRVEN MDISDEEEGG
481 APPPGSPQVL EEDEAELELQ KQLEKGRRLR QLQQLQQLRD SGEKVVEIVK KLESRQRGWE
541 EDEDPERKGA IVFNATSEFC RTLGEIPTYG LAGNREEQEE LMDFERDEER SANGGSESDG
601 EENIGWSTVN LDEEKQQQDF SASSTTILDE EPIVNRGLAA ALLLCQNKGL LETTVQKVAR
661 VKAPNKSLPS AVYCIEDKMA IDDKYSRREE YRGFTQDFKE KDGYKPDVKI EYVDETGRKL
721 TPKEAFRQLS HRFHGKGSGK MKTERRMKKL DEEALLKKMS SSDTPLGTVA LLQEKQKAQK
781 TPYIVLSGSG KSMNANTITKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SART1 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)
- 0.6
- Highest tissue expression
- 39 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 39 nTPM
- skeletal muscle: 33 nTPM
- spleen: 28 nTPM
- skin: 28 nTPM
- ovary: 25 nTPM
- endometrium: 25 nTPM
Single-cell type
- neutrophils: 71 nCPM
- syncytiotrophoblasts: 62 nCPM
- erythrocyte progenitors: 53 nCPM
- retinal pigment epithelial cells: 51 nCPM
- early primary spermatocytes: 47 nCPM
- cytotrophoblasts: 47 nCPM
Immune cell
- eosinophil: 8.1 nTPM
- T-reg: 5.4 nTPM
- memory CD4 T-cell: 4.8 nTPM
- memory CD8 T-cell: 4.4 nTPM
- gdT-cell: 4.3 nTPM
- neutrophil: 4 nTPM
Brain region
- white matter: 23 nTPM
- basal ganglia: 22 nTPM
- medulla oblongata: 22 nTPM
- cerebral cortex: 21 nTPM
- midbrain: 21 nTPM
- hypothalamus: 21 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about SART1.
Disease | ImmuneIEDB
Conditions an epitope on SART1 was assayed in.
- prostate cancer B and T cell
- prostate adenocarcinoma B and T cell
- melanoma T cell
- cholangiocarcinoma T cell
- pancreatic adenocarcinoma T cell
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)
- 0.34
- gnomAD pLI
- 0.88
- gnomAD missense Z
- 2.3
- DepMap mean gene effect
- -1.11
- DepMap dependency class
- common
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
- mRNA cis splicing, via spliceosome
- mRNA splicing, via spliceosome
- positive regulation of cytotoxic T cell differentiation
- spliceosomal snRNP assembly
- maturation of 5S rRNA
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- SNU66/SART1 family
- HIND motif
- SART-1 family
- HIND motif
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SART1 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 SART1 as an antibody target. Whether an autoantibody or antibody against SART1 could matter depends on whether native SART1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SART1 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 SART1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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