PRR5L
Proline-rich protein 5-like
Also known as: FLJ14213, PROTOR-2, PRR5L_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6MZQ0
- Gene
- PRR5L
- Ensembl
- ENSG00000135362
- Chromosome
- 11
- Canonical length
- 368 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Cytokinetic bridge,Cytosol
OverviewNCBI Gene
Enables ubiquitin protein ligase binding activity. Involved in several processes, including TORC2 signaling; regulation of fibroblast migration; and regulation of primary metabolic process. Part of TORC2 complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
368 residues, UniProt reviewed canonical sequence.
>Q6MZQ0|PRR5L
1 MTRGFAPILP VEFHKMGSFR RPRPRFMSSP VLSDLPRFQA ARQALQLSSS SAWNSVQTAV
61 INVFKGGGLQ SNELYALNEN IRRLLKSELG SFITDYFQNQ LLAKGLFFVE EKIKLCEGEN
121 RIEVLAEVWD HFFTETLPTL QAIFYPVQGQ ELTIRQISLL GFRDLVLLKV KLGDLLLLAQ
181 SKLPSSIVQM LLILQSVHEP TGPSESYLQL EELVKQVVSP FLGISGDRSF SGPTYTLARR
241 HSRVRPKVTV LNYASPITAV SRPLNEMVLT PLTEQEGEAY LEKCGSVRRH TVANAHSDIQ
301 LLAMATMMHS GLGEEASSEN KCLLLPPSFP PPHRQCSSEP NITDNPDGLE EGARGSQEGS
361 ELNCASLSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PRR5L 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.5
- Highest tissue expression
- 34 nTPM
Expression across tissuesHPA
Tissue
- spleen: 34 nTPM
- colon: 33 nTPM
- rectum: 26 nTPM
- spinal cord: 25 nTPM
- lung: 13 nTPM
- ovary: 12 nTPM
Single-cell type
- oligodendrocytes: 341 nCPM
- salivary ionocytes: 116 nCPM
- salivary duct cells: 109 nCPM
- nk-cells: 104 nCPM
- colonocytes: 88 nCPM
- lymphatic endothelial cells: 80 nCPM
Immune cell
- basophil: 36 nTPM
- gdT-cell: 35 nTPM
- memory CD8 T-cell: 30 nTPM
- eosinophil: 25 nTPM
- non-classical monocyte: 25 nTPM
- intermediate monocyte: 21 nTPM
Brain region
- white matter: 100 nTPM
- medulla oblongata: 85 nTPM
- pons: 63 nTPM
- basal ganglia: 63 nTPM
- spinal cord: 57 nTPM
- midbrain: 56 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)
- 0.64
- gnomAD pLI
- 0.07
- gnomAD missense Z
- 1.23
- DepMap mean gene effect
- 0.17
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cellular response to oxidative stress
- negative regulation of protein phosphorylation
- negative regulation of signal transduction
- phosphatidylinositol 3-kinase/protein kinase B signal transduction
- positive regulation of intracellular protein transport
- positive regulation of mRNA catabolic process
- positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction
- regulation of fibroblast migration
- TORC2 signaling
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PRR5L 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 PRR5L as an antibody target. Whether an autoantibody or antibody against PRR5L could matter depends on whether native PRR5L is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PRR5L 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 PRR5L as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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