SRPRB
Signal recognition particle receptor subunit beta
Also known as: APMCF1, SR-beta, SRPRB_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y5M8
- Gene
- SRPRB
- Ensembl
- ENSG00000144867
- Chromosome
- 3
- Canonical length
- 271 aa
- Protein class
- Predicted membrane proteins
- Subcellular location
- Plasma membrane
OverviewNCBI Gene
The protein encoded by this gene has similarity to mouse protein which is a subunit of the signal recognition particle receptor (SR). This subunit is a transmembrane GTPase belonging to the GTPase superfamily. It anchors alpha subunit, a peripheral membrane GTPase, to the ER membrane. SR is required for the cotranslational targeting of both secretory and membrane proteins to the ER membrane. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
271 residues, UniProt reviewed canonical sequence.
>Q9Y5M8|SRPRB
1 MASADSRRVA DGGGAGGTFQ PYLDTLRQEL QQTDPTLLSV VVAVLAVLLT LVFWKLIRSR
61 RSSQRAVLLV GLCDSGKTLL FVRLLTGLYR DTQTSITDSC AVYRVNNNRG NSLTLIDLPG
121 HESLRLQFLE RFKSSARAIV FVVDSAAFQR EVKDVAEFLY QVLIDSMGLK NTPSFLIACN
181 KQDIAMAKSA KLIQQQLEKE LNTLRVTRSA APSTLDSSST APAQLGKKGK EFEFSQLPLK
241 VEFLECSAKG GRGDVGSADI QDLEKWLAKI ALocalizationUniProt · AlphaFold · HPA
Whether an antibody against SRPRB 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.36
- Highest tissue expression
- 89 nTPM
Expression across tissuesHPA
Tissue
- pancreas: 89 nTPM
- liver: 56 nTPM
- salivary gland: 47 nTPM
- epididymis: 45 nTPM
- choroid plexus: 43 nTPM
- esophagus: 33 nTPM
Single-cell type
- plasma cells: 206 nCPM
- esophageal suprabasal cells: 150 nCPM
- oocytes: 143 nCPM
- pancreatic acinar cells: 129 nCPM
- breast lactating cells: 124 nCPM
- gastric progenitor cells: 115 nCPM
Immune cell
- MAIT T-cell: 73 nTPM
- gdT-cell: 54 nTPM
- plasmacytoid DC: 54 nTPM
- naive CD8 T-cell: 52 nTPM
- total PBMC: 50 nTPM
- memory CD8 T-cell: 48 nTPM
Brain region
- white matter: 35 nTPM
- choroid plexus: 32 nTPM
- midbrain: 27 nTPM
- medulla oblongata: 27 nTPM
- pons: 27 nTPM
- cerebral cortex: 26 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)
- 0.83
- gnomAD pLI
- 0.01
- gnomAD missense Z
- -0.01
- DepMap mean gene effect
- -0.66
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- protein targeting to ER
- SRP-dependent cotranslational protein targeting to membrane, signal sequence recognition
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Small GTPase superfamily, ARF type
- P-loop containing nucleoside triphosphate hydrolase
- Signal recognition particle receptor, beta subunit
- Signal recognition particle receptor beta subunit
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SRPRB 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 SRPRB as an antibody target. Whether an autoantibody or antibody against SRPRB could matter depends on whether native SRPRB is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SRPRB 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 SRPRB as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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