AGPAT5
1-acyl-sn-glycerol-3-phosphate acyltransferase epsilon
Also known as: FLJ11210, LPAAT-e, LPAAT-epsilon, LPLAT5, PLCE_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NUQ2
- Gene
- AGPAT5
- Ensembl
- ENSG00000155189
- Chromosome
- 8
- Canonical length
- 364 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted membrane proteins
- Subcellular location
- Mitochondria
OverviewNCBI Gene
This gene encodes a member of the 1-acylglycerol-3-phosphate O-acyltransferase family. This integral membrane protein converts lysophosphatidic acid to phosphatidic acid, the second step in de novo phospholipid biosynthesis. A pseudogene of this gene is present on the Y chromosome. [provided by RefSeq, Aug 2014]
Canonical amino-acid sequenceUniProt
364 residues, UniProt reviewed canonical sequence.
>Q9NUQ2|AGPAT5
1 MLLSLVLHTY SMRYLLPSVV LLGTAPTYVL AWGVWRLLSA FLPARFYQAL DDRLYCVYQS
61 MVLFFFENYT GVQILLYGDL PKNKENIIYL ANHQSTVDWI VADILAIRQN ALGHVRYVLK
121 EGLKWLPLYG CYFAQHGGIY VKRSAKFNEK EMRNKLQSYV DAGTPMYLVI FPEGTRYNPE
181 QTKVLSASQA FAAQRGLAVL KHVLTPRIKA THVAFDCMKN YLDAIYDVTV VYEGKDDGGQ
241 RRESPTMTEF LCKECPKIHI HIDRIDKKDV PEEQEHMRRW LHERFEIKDK MLIEFYESPD
301 PERRKRFPGK SVNSKLSIKK TLPSMLILSG LTAGMLMTDA GRKLYVNTWI YGTLLGCLWV
361 TIKALocalizationUniProt · AlphaFold · HPA
Whether an antibody against AGPAT5 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
- 3
- Mean surface accessibility (rSASA)
- 0.25
- Highest tissue expression
- 19 nTPM
Expression across tissuesHPA
Tissue
- spinal cord: 19 nTPM
- basal ganglia: 14 nTPM
- amygdala: 14 nTPM
- testis: 13 nTPM
- midbrain: 13 nTPM
- hippocampal formation: 13 nTPM
Single-cell type
- ependymal cells: 155 nCPM
- proximal tubule cells: 104 nCPM
- microglia: 83 nCPM
- oligodendrocyte progenitor cells: 76 nCPM
- other brain neurons: 75 nCPM
- astrocytes: 71 nCPM
Immune cell
- naive B-cell: 5.1 nTPM
- memory B-cell: 4.4 nTPM
- plasmacytoid DC: 4.4 nTPM
- NK-cell: 2.7 nTPM
- intermediate monocyte: 2.4 nTPM
- non-classical monocyte: 2.2 nTPM
Brain region
- white matter: 12 nTPM
- medulla oblongata: 11 nTPM
- spinal cord: 10 nTPM
- midbrain: 10 nTPM
- hypothalamus: 9.9 nTPM
- cerebellum: 9.3 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about AGPAT5.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 82 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
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)
- 0.98
- gnomAD pLI
- 0
- gnomAD missense Z
- -1.66
- DepMap mean gene effect
- 0.08
- 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
- CDP-diacylglycerol biosynthetic process
- hematopoietic progenitor cell differentiation
- phosphatidic acid biosynthetic process
- phosphatidylinositol acyl-chain remodeling
- phospholipid biosynthetic process
- acylglycerol metabolic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads AGPAT5 as an antibody target. Whether an autoantibody or antibody against AGPAT5 could matter depends on whether native AGPAT5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
AGPAT5 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 AGPAT5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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