ARF5
ADP-ribosylation factor 5
Also known as: ARF5_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P84085
- Gene
- ARF5
- Ensembl
- ENSG00000004059
- Chromosome
- 7
- Canonical length
- 180 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
OverviewNCBI Gene
This gene is a member of the human ADP-ribosylation factor (ARF) gene family. These genes encode small guanine nucleotide-binding proteins that stimulate the ADP-ribosyltransferase activity of cholera toxin and play a role in vesicular trafficking and as activators of phospholipase D. The gene products include 6 ARF proteins and 11 ARF-like proteins and constitute 1 family of the RAS superfamily. The ARF proteins are categorized as class I (ARF1, ARF2,and ARF3), class II (ARF4 and ARF5) and class III (ARF6). The members of each class share a common gene organization. [provided by RefSeq, Dec 2010]
Canonical amino-acid sequenceUniProt
180 residues, UniProt reviewed canonical sequence.
>P84085|ARF5
1 MGLTVSALFS RIFGKKQMRI LMVGLDAAGK TTILYKLKLG EIVTTIPTIG FNVETVEYKN
61 ICFTVWDVGG QDKIRPLWRH YFQNTQGLIF VVDSNDRERV QESADELQKM LQEDELRDAV
121 LLVFANKQDM PNAMPVSELT DKLGLQHLRS RTWYVQATCA TQGTGLYDGL DWLSHELSKRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ARF5 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.28
- Highest tissue expression
- 249 nTPM
Expression across tissuesHPA
Tissue
- esophagus: 249 nTPM
- cerebral cortex: 222 nTPM
- skin: 215 nTPM
- basal ganglia: 195 nTPM
- pancreas: 182 nTPM
- amygdala: 177 nTPM
Single-cell type
- esophageal apical cells: 280 nCPM
- oocytes: 263 nCPM
- epididymal principal cells: 230 nCPM
- esophageal suprabasal cells: 207 nCPM
- breast myoepithelial cells: 195 nCPM
- decidual stromal cells: 178 nCPM
Immune cell
- neutrophil: 450 nTPM
- myeloid DC: 410 nTPM
- total PBMC: 382 nTPM
- classical monocyte: 322 nTPM
- basophil: 290 nTPM
- eosinophil: 280 nTPM
Brain region
- cerebral cortex: 134 nTPM
- basal ganglia: 123 nTPM
- hippocampal formation: 112 nTPM
- amygdala: 106 nTPM
- hypothalamus: 104 nTPM
- thalamus: 100 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)
- 0.33
- gnomAD pLI
- 0.94
- gnomAD missense Z
- 2.28
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 8% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- intracellular protein transport
- retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum
- vesicle-mediated transport
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ARF5 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 ARF5 as an antibody target. Whether an autoantibody or antibody against ARF5 could matter depends on whether native ARF5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ARF5 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 ARF5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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