DDX1
ATP-dependent RNA helicase DDX1
Also known as: DBP-RB, DDX1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q92499
- Gene
- DDX1
- Ensembl
- ENSG00000079785
- Chromosome
- 2
- Canonical length
- 740 aa
- Protein class
- Enzymes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein that acts as an ATP-dependent RNA helicase that has been found to promote coronaviruses replication. [provided by RefSeq, Aug 2021]
Canonical amino-acid sequenceUniProt
740 residues, UniProt reviewed canonical sequence.
>Q92499|DDX1
1 MAAFSEMGVM PEIAQAVEEM DWLLPTDIQA ESIPLILGGG DVLMAAETGS GKTGAFSIPV
61 IQIVYETLKD QQEGKKGKTT IKTGASVLNK WQMNPYDRGS AFAIGSDGLC CQSREVKEWH
121 GCRATKGLMK GKHYYEVSCH DQGLCRVGWS TMQASLDLGT DKFGFGFGGT GKKSHNKQFD
181 NYGEEFTMHD TIGCYLDIDK GHVKFSKNGK DLGLAFEIPP HMKNQALFPA CVLKNAELKF
241 NFGEEEFKFP PKDGFVALSK APDGYIVKSQ HSGNAQVTQT KFLPNAPKAL IVEPSRELAE
301 QTLNNIKQFK KYIDNPKLRE LLIIGGVAAR DQLSVLENGV DIVVGTPGRL DDLVSTGKLN
361 LSQVRFLVLD EADGLLSQGY SDFINRMHNQ IPQVTSDGKR LQVIVCSATL HSFDVKKLSE
421 KIMHFPTWVD LKGEDSVPDT VHHVVVPVNP KTDRLWERLG KSHIRTDDVH AKDNTRPGAN
481 SPEMWSEAIK ILKGEYAVRA IKEHKMDQAI IFCRTKIDCD NLEQYFIQQG GGPDKKGHQF
541 SCVCLHGDRK PHERKQNLER FKKGDVRFLI CTDVAARGID IHGVPYVINV TLPDEKQNYV
601 HRIGRVGRAE RMGLAISLVA TEKEKVWYHV CSSRGKGCYN TRLKEDGGCT IWYNEMQLLS
661 EIEEHLNCTI SQVEPDIKVP VDEFDGKVTY GQKRAAGGGS YKGHVDILAP TVQELAALEK
721 EAQTSFLHLG YLPNQLFRTFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DDX1 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)
- 0.25
- Highest tissue expression
- 148 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 148 nTPM
- tongue: 126 nTPM
- parathyroid gland: 84 nTPM
- heart muscle: 82 nTPM
- kidney: 72 nTPM
- blood vessel: 60 nTPM
Single-cell type
- oocytes: 304 nCPM
- erythrocyte progenitors: 233 nCPM
- early primary spermatocytes: 180 nCPM
- hepatocytes: 156 nCPM
- late primary spermatocytes: 148 nCPM
- cytotrophoblasts: 145 nCPM
Immune cell
- intermediate monocyte: 42 nTPM
- non-classical monocyte: 42 nTPM
- naive CD4 T-cell: 40 nTPM
- NK-cell: 39 nTPM
- myeloid DC: 39 nTPM
- T-reg: 38 nTPM
Brain region
- cerebral cortex: 43 nTPM
- choroid plexus: 36 nTPM
- hypothalamus: 32 nTPM
- white matter: 32 nTPM
- medulla oblongata: 31 nTPM
- pons: 30 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)
- 0.28
- gnomAD pLI
- 0.99
- gnomAD missense Z
- 1.82
- DepMap mean gene effect
- -0.37
- 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
- defense response to virus
- double-strand break repair
- innate immune response
- positive regulation of canonical NF-kappaB signal transduction
- positive regulation of myeloid dendritic cell cytokine production
- protein localization to cytoplasmic stress granule
- regulation of translational initiation
- response to exogenous dsRNA
- spliceosomal complex assembly
- tRNA splicing, via endonucleolytic cleavage and ligation
Molecular functions
- ATP binding
- ATP hydrolysis activity
- chromatin binding
- DNA binding
- DNA/RNA helicase activity
- double-stranded RNA binding
- exonuclease activity
- nuclease activity
- poly(A) binding
- RNA binding
- RNA helicase activity
- transcription coregulator activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Helicase, C-terminal domain-like
- B30.2/SPRY domain
- SPRY domain
- DEAD/DEAH-box helicase domain
- Concanavalin A-like lectin/glucanase domain superfamily
- Helicase superfamily 1/2, ATP-binding domain
- RNA helicase, DEAD-box type, Q motif
- P-loop containing nucleoside triphosphate hydrolase
- B30.2/SPRY domain superfamily
- DEAD/DEAH box helicase
- Helicase conserved C-terminal domain
- SPRY domain
KeywordsUniProt
- Acetylation
- Activator
- Antiviral defense
- ATP-binding
- Cytoplasm
- DNA-binding
- Exonuclease
- Helicase
- Host-virus interaction
- Hydrolase
- Immunity
- Innate immunity
- Isopeptide bond
- Mitochondrion
- mRNA processing
- Nuclease
- Nucleotide-binding
- Nucleus
- Phosphoprotein
- RNA-binding
- Transcription
- Transcription regulation
- tRNA processing
- Ubl conjugation
InteractionsUniProt · HPA
Protein binding partners of DDX1 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 DDX1 as an antibody target. Whether an autoantibody or antibody against DDX1 could matter depends on whether native DDX1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DDX1 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 DDX1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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