Seroatlas · Human Serome Atlas

PSMD5

26S proteasome non-ATPase regulatory subunit 5

Also known as: KIAA0072, PSMD5_HUMAN, S5B

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

Protein identityUniProt · HPA

UniProt accession
Q16401
Gene
PSMD5
Ensembl
ENSG00000095261
Chromosome
9
Canonical length
504 aa
Protein class
Plasma proteins, Predicted intracellular proteins
Subcellular location
Nucleoplasm,Centrosome,Basal body,Cytosol,Connecting piece,Mid piece

OverviewNCBI Gene

The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. This gene encodes a non-ATPase subunit of the 19S regulator base that functions as a chaperone protein during 26S proteasome assembly. [provided by RefSeq, Jul 2012]

Canonical amino-acid sequenceUniProt

504 residues, UniProt reviewed canonical sequence.

>Q16401|PSMD5
     1  MAAQALALLR EVARLEAPLE ELRALHSVLQ AVPLNELRQQ AAELRLGPLF SLLNENHREK
    61  TTLCVSILER LLQAMEPVHV ARNLRVDLQR GLIHPDDSVK ILTLSQIGRI VENSDAVTEI
   121  LNNAELLKQI VYCIGGENLS VAKAAIKSLS RISLTQAGLE ALFESNLLDD LKSVMKTNDI
   181  VRYRVYELII EISSVSPESL NYCTTSGLVT QLLRELTGED VLVRATCIEM VTSLAYTHHG
   241  RQYLAQEGVI DQISNIIVGA DSDPFSSFYL PGFVKFFGNL AVMDSPQQIC ERYPIFVEKV
   301  FEMIESQDPT MIGVAVDTVG ILGSNVEGKQ VLQKTGTRFE RLLMRIGHQS KNAPVELKIR
   361  CLDAISSLLY LPPEQQTDDL LRMTESWFSS LSRDPLELFR GISSQPFPEL HCAALKVFTA
   421  IANQPWAQKL MFNSPGFVEY VVDRSVEHDK ASKDAKYELV KALANSKTIA EIFGNPNYLR
   481  LRTYLSEGPY YVKPVSTTAV EGAE

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against PSMD5 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)
0.25
Highest tissue expression
22 nTPM

Expression across tissuesHPA

Tissue

  • breast: 22 nTPM
  • bone marrow: 19 nTPM
  • liver: 19 nTPM
  • skin: 19 nTPM
  • tonsil: 18 nTPM
  • smooth muscle: 17 nTPM

Single-cell type

  • neutrophil progenitors: 92 nCPM
  • adrenal cortex cells: 76 nCPM
  • rod photoreceptor cells: 69 nCPM
  • pdcs: 67 nCPM
  • erythrocyte progenitors: 67 nCPM
  • myonuclei: 66 nCPM

Immune cell

  • T-reg: 33 nTPM
  • memory CD8 T-cell: 24 nTPM
  • non-classical monocyte: 24 nTPM
  • memory CD4 T-cell: 23 nTPM
  • memory B-cell: 22 nTPM
  • naive CD4 T-cell: 22 nTPM

Brain region

  • white matter: 26 nTPM
  • cerebellum: 25 nTPM
  • hypothalamus: 21 nTPM
  • pons: 20 nTPM
  • thalamus: 20 nTPM
  • midbrain: 20 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)
1.04
gnomAD pLI
0
gnomAD missense Z
0.29
DepMap mean gene effect
-0.04
DepMap dependency class
selective

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

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of PSMD5 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 PSMD5 as an antibody target. Whether an autoantibody or antibody against PSMD5 could matter depends on whether native PSMD5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

PSMD5 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 PSMD5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/PSMD5. 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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