PEX11A
Peroxisomal membrane protein 11A
Also known as: MGC119947, MGC138534, PEX11alpha, PMP28, PX11A_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75192
- Gene
- PEX11A
- Ensembl
- ENSG00000166821
- Chromosome
- 15
- Canonical length
- 247 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins, Predicted membrane proteins, Transporters
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene is a member of the PEX11 family, which is composed of membrane elongation factors involved in regulation of peroxisome maintenance and proliferation. This gene product interacts with peroxisomal membrane protein 19 and may respond to outside stimuli to increase peroxisome abundance. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2012]
Canonical amino-acid sequenceUniProt
247 residues, UniProt reviewed canonical sequence.
>O75192|PEX11A
1 MDAFTRFTNQ TQGRDRLFRA TQYTCMLLRY LLEPKAGKEK VVMKLKKLES SVSTGRKWFR
61 LGNVVHAIQA TEQSIHATDL VPRLCLTLAN LNRVIYFICD TILWVRSVGL TSGINKEKWR
121 TRAAHHYYYS LLLSLVRDLY EISLQMKRVT CDRAKKEKSA SQDPLWFSVA EEETEWLQSF
181 LLLLFRSLKQ HPPLLLDTVK NLCDILNPLD QLGIYKSNPG IIGLGGLVSS IAGMITVAYP
241 QMKLKTRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PEX11A 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
- 2
- Mean surface accessibility (rSASA)
- 0.33
- Highest tissue expression
- 37 nTPM
Expression across tissuesHPA
Tissue
- liver: 37 nTPM
- adipose tissue: 24 nTPM
- breast: 19 nTPM
- prostate: 17 nTPM
- skeletal muscle: 17 nTPM
- duodenum: 15 nTPM
Single-cell type
- late spermatids: 60 nCPM
- prostatic club cells: 57 nCPM
- adipocytes: 50 nCPM
- hepatocytes: 48 nCPM
- late primary spermatocytes: 42 nCPM
- prostatic hillock cells: 39 nCPM
Immune cell
- gdT-cell: 3.6 nTPM
- NK-cell: 3 nTPM
- naive CD8 T-cell: 2.6 nTPM
- eosinophil: 2.3 nTPM
- naive CD4 T-cell: 2.2 nTPM
- MAIT T-cell: 2 nTPM
Brain region
- choroid plexus: 21 nTPM
- hypothalamus: 13 nTPM
- basal ganglia: 11 nTPM
- midbrain: 11 nTPM
- thalamus: 11 nTPM
- amygdala: 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)
- 1.49
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.1
- DepMap mean gene effect
- 0.05
- 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
- brown fat cell differentiation
- peroxisome fission
- peroxisome membrane biogenesis
- peroxisome organization
- regulation of peroxisome size
- signal transduction
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PEX11A 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 PEX11A as an antibody target. Whether an autoantibody or antibody against PEX11A could matter depends on whether native PEX11A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PEX11A 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 PEX11A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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