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 EGAELocalizationUniProt · 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
- Armadillo-like helical
- Armadillo-type fold
- 26S proteasome non-ATPase regulatory subunit 5
- Proteasome non-ATPase 26S subunit
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.
Loading the interactive Seroatlas protein explorer...