PDCL3
Phosducin-like protein 3
Also known as: PDCL3_HUMAN, VIAF1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H2J4
- Gene
- PDCL3
- Ensembl
- ENSG00000115539
- Chromosome
- 2
- Canonical length
- 239 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
This gene encodes a member of the phosducin-like protein family and is a putative modulator of heterotrimeric G proteins. The protein shares extensive amino acid sequence homology with phosducin. Members of the phosducin-like protein family have been shown to bind to the beta-gamma subunits of G proteins. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
239 residues, UniProt reviewed canonical sequence.
>Q9H2J4|PDCL3
1 MQDPNADTEW NDILRKKGIL PPKESLKELE EEAEEEQRIL QQSVVKTYED MTLEELEDHE
61 DEFNEEDERA IEMYRRRRLA EWKATKLKNK FGEVLEISGK DYVQEVTKAG EGLWVILHLY
121 KQGIPLCALI NQHLSGLARK FPDVKFIKAI STTCIPNYPD RNLPTIFVYL EGDIKAQFIG
181 PLVFGGMNLT RDELEWKLSE SGAIMTDLEE NPKKPIEDVL LSSVRRSVLM KRDSDSEGDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PDCL3 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)
- 0.38
- Highest tissue expression
- 59 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 59 nTPM
- urinary bladder: 43 nTPM
- blood vessel: 38 nTPM
- smooth muscle: 36 nTPM
- epididymis: 35 nTPM
- skin: 35 nTPM
Single-cell type
- oocytes: 143 nCPM
- undifferentiated spermatogonia: 85 nCPM
- thymic myoid cells: 68 nCPM
- cytotrophoblasts: 68 nCPM
- esophageal suprabasal cells: 63 nCPM
- smooth muscle cells: 60 nCPM
Immune cell
- non-classical monocyte: 162 nTPM
- intermediate monocyte: 124 nTPM
- myeloid DC: 115 nTPM
- T-reg: 114 nTPM
- naive CD4 T-cell: 98 nTPM
- memory CD4 T-cell: 95 nTPM
Brain region
- midbrain: 28 nTPM
- thalamus: 23 nTPM
- medulla oblongata: 22 nTPM
- white matter: 22 nTPM
- pons: 21 nTPM
- cerebellum: 21 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)
- 1.35
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.45
- DepMap mean gene effect
- -0.38
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- actin cytoskeleton organization
- angiogenesis
- apoptotic process
- negative regulation of protein folding
- negative regulation of ubiquitin-dependent protein catabolic process
- positive regulation of angiogenesis
- positive regulation of endothelial cell proliferation
- positive regulation of gene expression
- protein folding
- protein stabilization
- regulation of peptidyl-tyrosine phosphorylation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PDCL3 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 PDCL3 as an antibody target. Whether an autoantibody or antibody against PDCL3 could matter depends on whether native PDCL3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PDCL3 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 PDCL3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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