PSMG1
Proteasome assembly chaperone 1
Also known as: c21-LRP, DSCR2, LRPC21, PAC1, PSMG1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O95456
- Gene
- PSMG1
- Ensembl
- ENSG00000183527
- Chromosome
- 21
- Canonical length
- 288 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Golgi apparatus,Cytosol
OverviewNCBI Gene
Enables molecular adaptor activity. Involved in chaperone-mediated protein complex assembly. Located in several cellular components, including Golgi apparatus; endoplasmic reticulum; and nucleoplasm. Part of protein folding chaperone complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
288 residues, UniProt reviewed canonical sequence.
>O95456|PSMG1
1 MAATFFGEVV KAPCRAGTED EEEEEEGRRE TPEDREVRLQ LARKREVRLL RRQTKTSLEV
61 SLLEKYPCSK FIIAIGNNAV AFLSSFVMNS GVWEEVGCAK LWNEWCRTTD TTHLSSTEAF
121 CVFYHLKSNP SVFLCQCSCY VAEDQQYQWL EKVFGSCPRK NMQITILTCR HVTDYKTSES
181 TGSLPSPFLR ALKTQNFKDS ACCPLLEQPN IVHDLPAAVL SYCQVWKIPA ILYLCYTDVM
241 KLDLITVEAF KPILSTRSLK GLVKNIPQST EILKKLMTTN EIQSNIYTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PSMG1 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)
- 0.31
- Highest tissue expression
- 38 nTPM
Expression across tissuesHPA
Tissue
- testis: 38 nTPM
- bone marrow: 16 nTPM
- liver: 15 nTPM
- skeletal muscle: 14 nTPM
- esophagus: 12 nTPM
- pancreas: 10 nTPM
Single-cell type
- late primary spermatocytes: 1,403 nCPM
- early spermatids: 539 nCPM
- oocytes: 350 nCPM
- migrating cytotrophoblasts: 143 nCPM
- early primary spermatocytes: 139 nCPM
- esophageal basal cells: 138 nCPM
Immune cell
- memory CD4 T-cell: 15 nTPM
- T-reg: 14 nTPM
- memory CD8 T-cell: 12 nTPM
- MAIT T-cell: 12 nTPM
- myeloid DC: 12 nTPM
- memory B-cell: 12 nTPM
Brain region
- cerebral cortex: 16 nTPM
- hippocampal formation: 14 nTPM
- basal ganglia: 12 nTPM
- white matter: 12 nTPM
- hypothalamus: 12 nTPM
- pons: 11 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)
- 0.92
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.5
- DepMap mean gene effect
- -0.53
- 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
- cerebellar granule cell precursor proliferation
- chaperone-mediated protein complex assembly
- proteasome core complex assembly
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Proteasome assembly chaperone 1
- Proteasome assembly chaperone 4
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PSMG1 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 PSMG1 as an antibody target. Whether an autoantibody or antibody against PSMG1 could matter depends on whether native PSMG1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PSMG1 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 PSMG1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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