Seroatlas · Human Serome Atlas

PFDN5

Prefoldin subunit 5

Also known as: MM-1, PFD5, PFD5_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
Q99471
Gene
PFDN5
Ensembl
ENSG00000123349
Chromosome
12
Canonical length
154 aa
Protein class
Predicted intracellular proteins
Subcellular location
Intermediate filaments,Cytosol

OverviewNCBI Gene

This gene encodes a member of the prefoldin alpha subunit family. The encoded protein is one of six subunits of prefoldin, a molecular chaperone complex that binds and stabilizes newly synthesized polypeptides, thereby allowing them to fold correctly. The complex, consisting of two alpha and four beta subunits, forms a double beta barrel assembly with six protruding coiled-coils. The encoded protein may also repress the transcriptional activity of the proto-oncogene c-Myc. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]

Canonical amino-acid sequenceUniProt

154 residues, UniProt reviewed canonical sequence.

>Q99471|PFDN5
     1  MAQSINITEL NLPQLEMLKN QLDQEVEFLS TSIAQLKVVQ TKYVEAKDCL NVLNKSNEGK
    61  ELLVPLTSSM YVPGKLHDVE HVLIDVGTGY YVEKTAEDAK DFFKRKIDFL TKQMEKIQPA
   121  LQEKHAMKQA VMEMMSQKIQ QLTALGAAQA TAKA

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against PFDN5 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)
0.39
Highest tissue expression
1,060 nTPM

Expression across tissuesHPA

Tissue

  • choroid plexus: 1,060 nTPM
  • ovary: 964 nTPM
  • spinal cord: 915 nTPM
  • amygdala: 898 nTPM
  • midbrain: 898 nTPM
  • epididymis: 818 nTPM

Single-cell type

  • papillary tip epithelial cells: 62 nCPM
  • renal collecting duct principal cells: 53 nCPM
  • brain excitatory neurons: 51 nCPM
  • oligodendrocytes: 49 nCPM
  • other brain neurons: 49 nCPM
  • astrocytes: 49 nCPM

Immune cell

  • total PBMC: 8,669 nTPM
  • memory B-cell: 3,723 nTPM
  • naive B-cell: 3,385 nTPM
  • naive CD4 T-cell: 3,158 nTPM
  • classical monocyte: 2,771 nTPM
  • naive CD8 T-cell: 2,541 nTPM

Brain region

  • spinal cord: 301 nTPM
  • thalamus: 284 nTPM
  • white matter: 272 nTPM
  • basal ganglia: 254 nTPM
  • medulla oblongata: 241 nTPM
  • hypothalamus: 239 nTPM

ReferencesPubMed · IEDB

Publications for PFDN5 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)
1.33
gnomAD pLI
0
gnomAD missense Z
0.1
DepMap mean gene effect
-0.78
DepMap dependency class
common

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

Biological processes

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of PFDN5 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 PFDN5 as an antibody target. Whether an autoantibody or antibody against PFDN5 could matter depends on whether native PFDN5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

PFDN5 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 PFDN5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/PFDN5. 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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