HELQ
Helicase POLQ-like
Also known as: Hel308, HELQ_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8TDG4
- Gene
- HELQ
- Ensembl
- ENSG00000163312
- Chromosome
- 4
- Canonical length
- 1101 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear speckles
- Quaternary structure
- Homodimer
OverviewNCBI Gene
HEL308 is a single-stranded DNA-dependent ATPase and DNA helicase (Marini and Wood, 2002 [PubMed 11751861]).[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
1101 residues, UniProt reviewed canonical sequence.
>Q8TDG4|HELQ
1 MDECGSRIRR RVSLPKRNRP SLGCIFGAPT AAELVPGDEG KEEEEMVAEN RRRKTAGVLP
61 VEVQPLLLSD SPECLVLGGG DTNPDLLRHM PTDRGVGDQP NDSEVDMFGD YDSFTENSFI
121 AQVDDLEQKY MQLPEHKKHA TDFATENLCS ESIKNKLSIT TIGNLTELQT DKHTENQSGY
181 EGVTIEPGAD LLYDVPSSQA IYFENLQNSS NDLGDHSMKE RDWKSSSHNT VNEELPHNCI
241 EQPQQNDESS SKVRTSSDMN RRKSIKDHLK NAMTGNAKAQ TPIFSRSKQL KDTLLSEEIN
301 VAKKTVESSS NDLGPFYSLP SKVRDLYAQF KGIEKLYEWQ HTCLTLNSVQ ERKNLIYSLP
361 TSGGKTLVAE ILMLQELLCC RKDVLMILPY VAIVQEKISG LSSFGIELGF FVEEYAGSKG
421 RFPPTKRREK KSLYIATIEK GHSLVNSLIE TGRIDSLGLV VVDELHMIGE GSRGATLEMT
481 LAKILYTSKT TQIIGMSATL NNVEDLQKFL QAEYYTSQFR PVELKEYLKI NDTIYEVDSK
541 AENGMTFSRL LNYKYSDTLK KMDPDHLVAL VTEVIPNYSC LVFCPSKKNC ENVAEMICKF
601 LSKEYLKHKE KEKCEVIKNL KNIGNGNLCP VLKRTIPFGV AYHHSGLTSD ERKLLEEAYS
661 TGVLCLFTCT STLAAGVNLP ARRVILRAPY VAKEFLKRNQ YKQMIGRAGR AGIDTIGESI
721 LILQEKDKQQ VLELITKPLE NCYSHLVQEF TKGIQTLFLS LIGLKIATNL DDIYHFMNGT
781 FFGVQQKVLL KEKSLWEITV ESLRYLTEKG LLQKDTIYKS EEEVQYNFHI TKLGRASFKG
841 TIDLAYCDIL YRDLKKGLEG LVLESLLHLI YLTTPYDLVS QCNPDWMIYF RQFSQLSPAE
901 QNVAAILGVS ESFIGKKASG QAIGKKVDKN VVNRLYLSFV LYTLLKETNI WTVSEKFNMP
961 RGYIQNLLTG TASFSSCVLH FCEELEEFWV YRALLVELTK KLTYCVKAEL IPLMEVTGVL
1021 EGRAKQLYSA GYKSLMHLAN ANPEVLVRTI DHLSRRQAKQ IVSSAKMLLH EKAEALQEEV
1081 EELLRLPSDF PGAVASSTDK ALocalizationUniProt · AlphaFold · HPA
Whether an antibody against HELQ 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)
- 0.35
- Highest tissue expression
- 8.7 nTPM
Expression across tissuesHPA
Tissue
- lymph node: 8.7 nTPM
- adrenal gland: 8.4 nTPM
- tongue: 7.6 nTPM
- thymus: 7.4 nTPM
- tonsil: 7.1 nTPM
- ovary: 7 nTPM
Single-cell type
- adrenal cortex cells: 145 nCPM
- b-cells: 60 nCPM
- myonuclei: 59 nCPM
- microglia: 50 nCPM
- neutrophil progenitors: 49 nCPM
- thymocytes: 48 nCPM
Immune cell
- naive CD4 T-cell: 5.6 nTPM
- naive B-cell: 5.1 nTPM
- naive CD8 T-cell: 4.8 nTPM
- T-reg: 4.5 nTPM
- eosinophil: 3.6 nTPM
- NK-cell: 3.6 nTPM
Brain region
- choroid plexus: 10 nTPM
- cerebellum: 8.5 nTPM
- white matter: 6.2 nTPM
- basal ganglia: 5.5 nTPM
- pons: 5.3 nTPM
- spinal cord: 5.3 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about HELQ.
Disease | ImmuneIEDB
Conditions an epitope on HELQ was assayed in.
- ankylosing spondylitis 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)
- 0.76
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.6
- DepMap mean gene effect
- -0.06
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- DNA double-strand break processing involved in repair via single-strand annealing
- double-strand break repair via alternative nonhomologous end joining
- double-strand break repair via homologous recombination
- double-strand break repair via synthesis-dependent strand annealing
- positive regulation of double-strand break repair via homologous recombination
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Helicase, C-terminal domain-like
- DEAD/DEAH-box helicase domain
- Helicase superfamily 1/2, ATP-binding domain
- P-loop containing nucleoside triphosphate hydrolase
- Winged helix DNA-binding domain superfamily
- DNA polymerase theta-like, helix-turn-helix domain
- POLQ-like, helical domain
- Helicase Hel308/SKI2-like
- DEAD/DEAH box helicase
- Helicase conserved C-terminal domain
- Helix-turn-helix domain
- DNA_pol_Q helicase like region helical domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of HELQ 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 HELQ as an antibody target. Whether an autoantibody or antibody against HELQ could matter depends on whether native HELQ is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HELQ 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 HELQ as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...