ARAP3
Arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 3
Also known as: ARAP3_HUMAN, CENTD3, DRAG1, FLJ21065
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8WWN8
- Gene
- ARAP3
- Ensembl
- ENSG00000120318
- Chromosome
- 5
- Canonical length
- 1544 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
This gene encodes a phosphoinositide binding protein containing ARF-GAP, RHO-GAP, RAS-associating, and pleckstrin homology domains. The ARF-GAP and RHO-GAP domains cooperate in mediating rearrangements in the cell cytoskeleton and cell shape. It is a specific PtdIns(3,4,5)P3/PtdIns(3,4)P2-stimulated Arf6-GAP protein. An alternatively spliced transcript has been found for this gene, but its biological validity has not been determined. [provided by RefSeq, Sep 2015]
Canonical amino-acid sequenceUniProt
1544 residues, UniProt reviewed canonical sequence.
>Q8WWN8|ARAP3
1 MAAPQDLDIA VWLATVHLEQ YADTFRRHGL ATAGAARGLG HEELKQLGIS ATGHRKRILR
61 LLQTGTEEGS LDPKSDSAME PSPSPAPQAQ PPKPVPKPRT VFGGLSGPAT TQRPGLSPAL
121 GGPGVSRSPE PSPRPPPLPT SSSEQSSALN TVEMMPNSIY FGLDSRGRAQ AAQDKAPDSS
181 QISAPTPALR PTTGTVHIMD PGCLYYGVQP VGTPGAPDRR ESRGVCQGRA EHRLSRQDLE
241 AREDAGYASL ELPGDSTLLS PTLETEETSD DLISPYASFS FTADRLTPLL SGWLDKLSPQ
301 GNYVFQRRFV QFNGRSLMYF GSDKDPFPKG VIPLTAIEMT RSSKDNKFQV ITGQRVFVFR
361 TESEAQRDMW CSTLQSCLKE QRLLGHPRPP QPPRPLRTGM LELRGHKAKV FAALSPGELA
421 LYKSEQAFSL GIGICFIELQ GCSVRETKSR SFDLLTPHRC FSFTAESGGA RQSWAAALQE
481 AVTETLSDYE VAEKIWSNRA NRQCADCGSS RPDWAAVNLG VVICKQCAGQ HRALGSGISK
541 VQSLKLDTSV WSNEIVQLFI VLGNDRANRF WAGTLPPGEG LHPDATPGPR GEFISRKYRL
601 GLFRKPHPQY PDHSQLLQAL CAAVARPNLL KNMTQLLCVE AFEGEEPWFP PAPDGSCPGL
661 LPSDPSPGVY NEVVVRATYS GFLYCSPVSN KAGPSPPRRG RDAPPRLWCV LGAALEMFAS
721 ENSPEPLSLI QPQDIVCLGV SPPPTDPGDR FPFSFELILA GGRIQHFGTD GADSLEAWTS
781 AVGKWFSPLS CHQLLGPGLL RLGRLWLRSP SHTAPAPGLW LSGFGLLRGD HLFLCSAPGP
841 GPPAPEDMVH LRRLQEISVV SAADTPDKKE HLVLVETGRT LYLQGEGRLD FTAWNAAIGG
901 AAGGGGTGLQ EQQMSRGDIP IIVDACISFV TQHGLRLEGV YRKGGARARS LRLLAEFRRD
961 ARSVKLRPGE HFVEDVTDTL KRFFRELDDP VTSARLLPRW REAAELPQKN QRLEKYKDVI
1021 GCLPRVNRRT LATLIGHLYR VQKCAALNQM CTRNLALLFA PSVFQTDGRG EHEVRVLQEL
1081 IDGYISVFDI DSDQVAQIDL EVSLITTWKD VQLSQAGDLI MEVYIEQQLP DNCVTLKVSP
1141 TLTAEELTNQ VLEMRGTAAG MDLWVTFEIR EHGELERPLH PKEKVLEQAL QWCQLPEPCS
1201 ASLLLKKVPL AQAGCLFTGI RRESPRVGLL RCREEPPRLL GSRFQERFFL LRGRCLLLLK
1261 EKKSSKPERE WPLEGAKVYL GIRKKLKPPT PWGFTLILEK MHLYLSCTDE DEMWDWTTSI
1321 LKAQHDDQQP VVLRRHSSSD LARQKFGTMP LLPIRGDDSG ATLLSANQTL RRLHNRRTLS
1381 MFFPMKSSQG SVEEQEELEE PVYEEPVYEE VGAFPELIQD TSTSFSTTRE WTVKPENPLT
1441 SQKSLDQPFL SKSSTLGQEE RPPEPPPGPP SKSSPQARGS LEEQLLQELS SLILRKGETT
1501 AGLGSPSQPS SPQSPSPTGL PTQTPGFPTQ PPCTSSPPSS QPLTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ARAP3 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.4
- Highest tissue expression
- 15 nTPM
Expression across tissuesHPA
Tissue
- lung: 15 nTPM
- heart muscle: 14 nTPM
- placenta: 11 nTPM
- adipose tissue: 11 nTPM
- breast: 9.5 nTPM
- cervix: 8.6 nTPM
Single-cell type
- neutrophils: 133 nCPM
- retinal horizontal cells: 128 nCPM
- vascular endothelial cells: 89 nCPM
- lymphatic endothelial cells: 63 nCPM
- prostatic hillock cells: 30 nCPM
- neutrophil progenitors: 28 nCPM
Immune cell
- eosinophil: 3.3 nTPM
- neutrophil: 2.1 nTPM
- classical monocyte: 0.5 nTPM
- non-classical monocyte: 0.4 nTPM
- basophil: 0.3 nTPM
- intermediate monocyte: 0.2 nTPM
Brain region
- cerebral cortex: 14 nTPM
- thalamus: 14 nTPM
- cerebellum: 12 nTPM
- amygdala: 11 nTPM
- basal ganglia: 11 nTPM
- midbrain: 10 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)
- 0.43
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.82
- DepMap mean gene effect
- -0.01
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cytoskeleton organization
- regulation of actin cytoskeleton organization
- signal transduction
- vesicle-mediated transport
Molecular functions
- phosphatidylinositol-3,4,5-trisphosphate binding
- phosphatidylinositol-3,4-bisphosphate binding
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Ras-associating domain
- Rho GTPase-activating protein domain
- Arf GTPase activating protein
- Sterile alpha motif domain
- Pleckstrin homology domain
- Rho GTPase activation protein
- PH-like domain superfamily
- Sterile alpha motif/pointed domain superfamily
- Ubiquitin-like domain superfamily
- ARFGAP/RecO-like zinc finger
- ARAP, RhoGAP domain
- ArfGAP domain superfamily
- Arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein
- PH domain
- RhoGAP domain
- Ras association (RalGDS/AF-6) domain
- Putative GTPase activating protein for Arf
- SAM domain (Sterile alpha motif)
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ARAP3 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 ARAP3 as an antibody target. Whether an autoantibody or antibody against ARAP3 could matter depends on whether native ARAP3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ARAP3 is annotated at the cell surface, where native ARAP3 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label ARAP3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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