DDX43
Probable ATP-dependent RNA helicase DDX43
Also known as: CT13, DDX43_HUMAN, DKFZp434H2114, HAGE
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NXZ2
- Gene
- DDX43
- Ensembl
- ENSG00000080007
- Chromosome
- 6
- Canonical length
- 648 aa
- Protein class
- Enzymes, Predicted intracellular proteins
OverviewNCBI Gene
The protein encoded by this gene is an ATP-dependent RNA helicase in the DEAD-box family and displays tumor-specific expression. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
648 residues, UniProt reviewed canonical sequence.
>Q9NXZ2|DDX43
1 MSHHGGAPKA STWVVASRRS STVSRAPERR PAEELNRTGP EGYSVGRGGR WRGTSRPPEA
61 VAAGHEELPL CFALKSHFVG AVIGRGGSKI KNIQSTTNTT IQIIQEQPES LVKIFGSKAM
121 QTKAKAVIDN FVKKLEENYN SECGIDTAFQ PSVGKDGSTD NNVVAGDRPL IDWDQIREEG
181 LKWQKTKWAD LPPIKKNFYK ESTATSAMSK VEADSWRKEN FNITWDDLKD GEKRPIPNPT
241 CTFDDAFQCY PEVMENIKKA GFQKPTPIQS QAWPIVLQGI DLIGVAQTGT GKTLCYLMPG
301 FIHLVLQPSL KGQRNRPGML VLTPTRELAL QVEGECCKYS YKGLRSVCVY GGGNRDEQIE
361 ELKKGVDIII ATPGRLNDLQ MSNFVNLKNI TYLVLDEADK MLDMGFEPQI MKILLDVRPD
421 RQTVMTSATW PHSVHRLAQS YLKEPMIVYV GTLDLVAVSS VKQNIIVTTE EEKWSHMQTF
481 LQSMSSTDKV IVFVSRKAVA DHLSSDLILG NISVESLHGD REQRDREKAL ENFKTGKVRI
541 LIATDLASRG LDVHDVTHVY NFDFPRNIEE YVHRIGRTGR AGRTGVSITT LTRNDWRVAS
601 ELINILERAN QSIPEELVSM AERFKAHQQK REMERKMERP QGRPKKFHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DDX43 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.34
- Highest tissue expression
- 18 nTPM
Expression across tissuesHPA
Tissue
- testis: 18 nTPM
- placenta: 4.6 nTPM
- salivary gland: 1.7 nTPM
- seminal vesicle: 1.7 nTPM
- stomach: 1.6 nTPM
- blood vessel: 1.3 nTPM
Single-cell type
- oocytes: 97 nCPM
- undifferentiated spermatogonia: 81 nCPM
- late primary spermatocytes: 62 nCPM
- early primary spermatocytes: 50 nCPM
- differentiating spermatogonia: 47 nCPM
- cytotrophoblasts: 29 nCPM
Immune cell
- gdT-cell: 1 nTPM
- naive B-cell: 1 nTPM
- eosinophil: 0.9 nTPM
- memory B-cell: 0.9 nTPM
- memory CD8 T-cell: 0.9 nTPM
- MAIT T-cell: 0.7 nTPM
Brain region
- white matter: 1.8 nTPM
- medulla oblongata: 1.7 nTPM
- pons: 1.6 nTPM
- cerebral cortex: 1.1 nTPM
- thalamus: 1.1 nTPM
- hypothalamus: 1 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)
- 0.59
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.27
- DepMap mean gene effect
- -0.21
- 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
Molecular functions
Protein domainsUniProt · Pfam · InterPro
- ATP-dependent RNA helicase DEAD-box, conserved site
- Helicase, C-terminal domain-like
- K Homology domain
- K Homology domain, type 1
- DEAD/DEAH-box helicase domain
- Helicase superfamily 1/2, ATP-binding domain
- RNA helicase, DEAD-box type, Q motif
- P-loop containing nucleoside triphosphate hydrolase
- K Homology domain, type 1 superfamily
- KH domain
- DEAD/DEAH box helicase
- Helicase conserved C-terminal domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads DDX43 as an antibody target. Whether an autoantibody or antibody against DDX43 could matter depends on whether native DDX43 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DDX43 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 DDX43 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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