Seroatlas · Human Serome Atlas

PDCD1

Programmed cell death protein 1

Also known as: CD279, hSLE1, PD-1, PD1, PDCD1_HUMAN, SLEB2

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q15116
Gene
PDCD1
Ensembl
ENSG00000188389
Chromosome
2
Canonical length
288 aa
Protein class
CD markers, Disease related genes, FDA approved drug targets, Human disease related genes, Predicted intracellular proteins, Predicted membrane proteins, Transporters

OverviewNCBI Gene

Programmed cell death protein 1 (PDCD1) is an immune-inhibitory receptor expressed in activated T cells; it is involved in the regulation of T-cell functions, including those of effector CD8+ T cells. In addition, this protein can also promote the differentiation of CD4+ T cells into T regulatory cells. PDCD1 is expressed in many types of tumors including melanomas, and has demonstrated to play a role in anti-tumor immunity. Moreover, this protein has been shown to be involved in safeguarding against autoimmunity, however, it can also contribute to the inhibition of effective anti-tumor and anti-microbial immunity. [provided by RefSeq, Aug 2020]

Canonical amino-acid sequenceUniProt

288 residues, UniProt reviewed canonical sequence.

>Q15116|PDCD1
     1  MQIPQAPWPV VWAVLQLGWR PGWFLDSPDR PWNPPTFSPA LLVVTEGDNA TFTCSFSNTS
    61  ESFVLNWYRM SPSNQTDKLA AFPEDRSQPG QDCRFRVTQL PNGRDFHMSV VRARRNDSGT
   121  YLCGAISLAP KAQIKESLRA ELRVTERRAE VPTAHPSPSP RPAGQFQTLV VGVVGGLLGS
   181  LVLLVWVLAV ICSRAARGTI GARRTGQPLK EDPSAVPVFS VDYGELDFQW REKTPEPPVP
   241  CVPEQTEYAT IVFPSGMGTS SPARRGSADG PRSAQPLRPE DGHCSWPL

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against PDCD1 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
1
Mean surface accessibility (rSASA)
0.53
Highest tissue expression
15 nTPM

Expression across tissuesHPA

Tissue

  • lymph node: 15 nTPM
  • spleen: 6.7 nTPM
  • heart muscle: 6.4 nTPM
  • tonsil: 3.8 nTPM
  • small intestine: 3.6 nTPM
  • appendix: 3 nTPM

Single-cell type

  • t-cells: 2 nCPM
  • brain inhibitory neurons: 0.2 nCPM
  • distal convoluted tubule cells: 0.2 nCPM
  • b-cells: 0.1 nCPM
  • lactotrophs: 0.1 nCPM
  • loop of henle epithelial cells: 0.1 nCPM

Immune cell

  • memory CD8 T-cell: 12 nTPM
  • memory CD4 T-cell: 8.7 nTPM
  • MAIT T-cell: 4.8 nTPM
  • gdT-cell: 4.4 nTPM
  • T-reg: 4.3 nTPM
  • total PBMC: 2.1 nTPM

Brain region

  • midbrain: 3.1 nTPM
  • thalamus: 1 nTPM
  • choroid plexus: 0.7 nTPM
  • pons: 0.6 nTPM
  • white matter: 0.6 nTPM
  • basal ganglia: 0.5 nTPM

DiseaseUniProt · ClinVar · IEDB · PubMed

Four sources answering four different questions about PDCD1.

Disease | AllUniProt

Conditions PDCD1 is implicated in, by any mechanism.

ReferencesPubMed · IEDB

Publications for PDCD1 from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.

Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.

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)
0.66
gnomAD pLI
0.42
gnomAD missense Z
1.29
DepMap mean gene effect
-0.04
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

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of PDCD1 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 PDCD1 as an antibody target. Whether an autoantibody or antibody against PDCD1 could matter depends on whether native PDCD1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

PDCD1 is annotated at the cell surface, where native PDCD1 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 PDCD1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/PDCD1. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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