RECQL5
ATP-dependent DNA helicase Q5
Also known as: FLJ90603, RecQ5, RECQ5_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O94762
- Gene
- RECQL5
- Ensembl
- ENSG00000108469
- Chromosome
- 17
- Canonical length
- 991 aa
- Protein class
- Enzymes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
The protein encoded by this gene is a helicase that is important for genome stability. The encoded protein also prevents aberrant homologous recombination by displacing RAD51 from ssDNA. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2011]
Canonical amino-acid sequenceUniProt
991 residues, UniProt reviewed canonical sequence.
>O94762|RECQL5
1 MSSHHTTFPF DPERRVRSTL KKVFGFDSFK TPLQESATMA VVKGNKDVFV CMPTGAGKSL
61 CYQLPALLAK GITIVVSPLI ALIQDQVDHL LTLKVRVSSL NSKLSAQERK ELLADLEREK
121 PQTKILYITP EMAASSSFQP TLNSLVSRHL LSYLVVDEAH CVSQWGHDFR PDYLRLGALR
181 SRLGHAPCVA LTATATPQVQ EDVFAALHLK KPVAIFKTPC FRANLFYDVQ FKELISDPYG
241 NLKDFCLKAL GQEADKGLSG CGIVYCRTRE ACEQLAIELS CRGVNAKAYH AGLKASERTL
301 VQNDWMEEKV PVIVATISFG MGVDKANVRF VAHWNIAKSM AGYYQESGRA GRDGKPSWCR
361 LYYSRNDRDQ VSFLIRKEVA KLQEKRGNKA SDKATIMAFD ALVTFCEELG CRHAAIAKYF
421 GDALPACAKG CDHCQNPTAV RRRLEALERS SSWSKTCIGP SQGNGFDPEL YEGGRKGYGD
481 FSRYDEGSGG SGDEGRDEAH KREWNLFYQK QMQLRKGKDP KIEEFVPPDE NCPLKEASSR
541 RIPRLTVKAR EHCLRLLEEA LSSNRQSTRT ADEADLRAKA VELEHETFRN AKVANLYKAS
601 VLKKVADIHR ASKDGQPYDM GGSAKSCSAQ AEPPEPNEYD IPPASHVYSL KPKRVGAGFP
661 KGSCPFQTAT ELMETTRIRE QAPQPERGGE HEPPSRPCGL LDEDGSEPLP GPRGEVPGGS
721 AHYGGPSPEK KAKSSSGGSS LAKGRASKKQ QLLATAAHKD SQSIARFFCR RVESPALLAS
781 APEAEGACPS CEGVQGPPMA PEKYTGEEDG AGGHSPAPPQ TEECLRERPS TCPPRDQGTP
841 EVQPTPAKDT WKGKRPRSQQ ENPESQPQKR PRPSAKPSVV AEVKGSVSAS EQGTLNPTAQ
901 DPFQLSAPGV SLKEAANVVV KCLTPFYKEG KFASKELFKG FARHLSHLLT QKTSPGRSVK
961 EEAQNLIRHF FHGRARCESE ADWHGLCGPQ RLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RECQL5 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)
- 0.43
- Highest tissue expression
- 22 nTPM
Expression across tissuesHPA
Tissue
- stomach: 22 nTPM
- small intestine: 22 nTPM
- duodenum: 21 nTPM
- kidney: 21 nTPM
- skin: 20 nTPM
- pituitary gland: 20 nTPM
Single-cell type
- esophageal apical cells: 118 nCPM
- foveolar cells: 88 nCPM
- cardiomyocytes: 76 nCPM
- renal collecting duct intercalated cells: 46 nCPM
- renal collecting duct principal cells: 43 nCPM
- salivary duct cells: 41 nCPM
Immune cell
- plasmacytoid DC: 16 nTPM
- basophil: 6 nTPM
- eosinophil: 4.5 nTPM
- naive B-cell: 4.3 nTPM
- intermediate monocyte: 4.1 nTPM
- NK-cell: 4 nTPM
Brain region
- white matter: 35 nTPM
- thalamus: 27 nTPM
- cerebral cortex: 27 nTPM
- basal ganglia: 26 nTPM
- medulla oblongata: 25 nTPM
- midbrain: 24 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)
- 0.98
- gnomAD pLI
- 0
- gnomAD missense Z
- 0
- DepMap mean gene effect
- 0.02
- 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
- cell division
- cellular response to camptothecin
- cellular response to xenobiotic stimulus
- chromosome separation
- DNA metabolic process
- DNA repair
- DNA replication
- double-strand break repair via homologous recombination
- mitotic cell cycle
- negative regulation of double-strand break repair via homologous recombination
- negative regulation of transcription elongation by RNA polymerase II
- replication-born double-strand break repair via sister chromatid exchange
- mitotic DNA-templated DNA replication
Molecular functions
- 3'-5' DNA helicase activity
- ATP binding
- ATP hydrolysis activity
- DNA binding
- DNA helicase activity
- four-way junction helicase activity
- helicase activity
- identical protein binding
- metal ion binding
- RNA polymerase II complex binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Helicase, C-terminal domain-like
- DNA/RNA helicase, ATP-dependent, DEAH-box type, conserved site
- DNA helicase, ATP-dependent, RecQ type
- DEAD/DEAH-box helicase domain
- Set2 Rpb1 interacting domain
- Helicase superfamily 1/2, ATP-binding domain
- P-loop containing nucleoside triphosphate hydrolase
- ATP-dependent DNA helicase RecQ, zinc-binding domain
- DEAD/DEAH box helicase
- Helicase conserved C-terminal domain
- SRI (Set2 Rpb1 interacting) domain
- RecQ zinc-binding
- RecQ helicase-like 5
- RecQ helicase protein-like 5 (RecQ5)
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RECQL5 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 RECQL5 as an antibody target. Whether an autoantibody or antibody against RECQL5 could matter depends on whether native RECQL5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RECQL5 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 RECQL5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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