PPIL3
Peptidyl-prolyl cis-trans isomerase-like 3
Also known as: CyPJ, PPIL3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H2H8
- Gene
- PPIL3
- Ensembl
- ENSG00000240344
- Chromosome
- 2
- Canonical length
- 161 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Nucleoli
OverviewNCBI Gene
This gene encodes a member of the cyclophilin family. Cyclophilins catalyze the cis-trans isomerization of peptidylprolyl imide bonds in oligopeptides. They have been proposed to act either as catalysts or as molecular chaperones in protein-folding events. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2008]
Canonical amino-acid sequenceUniProt
161 residues, UniProt reviewed canonical sequence.
>Q9H2H8|PPIL3
1 MSVTLHTDVG DIKIEVFCER TPKTCENFLA LCASNYYNGC IFHRNIKGFM VQTGDPTGTG
61 RGGNSIWGKK FEDEYSEYLK HNVRGVVSMA NNGPNTNGSQ FFITYGKQPH LDMKYTVFGK
121 VIDGLETLDE LEKLPVNEKT YRPLNDVHIK DITIHANPFA QLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PPIL3 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
- 25 nTPM
Expression across tissuesHPA
Tissue
- ovary: 25 nTPM
- tonsil: 24 nTPM
- thymus: 24 nTPM
- lymph node: 23 nTPM
- spinal cord: 20 nTPM
- bone marrow: 19 nTPM
Single-cell type
- late primary spermatocytes: 141 nCPM
- gastric chief cells: 83 nCPM
- megakaryocytes: 74 nCPM
- extravillous trophoblasts: 73 nCPM
- migrating cytotrophoblasts: 71 nCPM
- decidual stromal cells: 68 nCPM
Immune cell
- memory B-cell: 34 nTPM
- myeloid DC: 30 nTPM
- basophil: 29 nTPM
- T-reg: 29 nTPM
- NK-cell: 29 nTPM
- naive CD8 T-cell: 26 nTPM
Brain region
- white matter: 13 nTPM
- cerebellum: 12 nTPM
- hypothalamus: 12 nTPM
- cerebral cortex: 11 nTPM
- pons: 11 nTPM
- medulla oblongata: 10 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)
- 0.4
- gnomAD pLI
- 0.9
- gnomAD missense Z
- 0.15
- DepMap mean gene effect
- -0.07
- DepMap dependency class
- selective
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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Cyclophilin-type peptidyl-prolyl cis-trans isomerase domain
- Cyclophilin-type peptidyl-prolyl cis-trans isomerase, conserved site
- Cyclophilin-type peptidyl-prolyl cis-trans isomerase
- Cyclophilin-like domain superfamily
- Cyclophilin-type peptidyl-prolyl cis-trans isomerase, cyclophilin A-like
- Cyclophilin type peptidyl-prolyl cis-trans isomerase/CLD
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PPIL3 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 PPIL3 as an antibody target. Whether an autoantibody or antibody against PPIL3 could matter depends on whether native PPIL3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PPIL3 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 PPIL3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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