AGPAT3
1-acyl-sn-glycerol-3-phosphate acyltransferase gamma
Also known as: LPAAT-gamma, LPAAT3, LPLAT3, PLCC_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NRZ7
- Gene
- AGPAT3
- Ensembl
- ENSG00000160216
- Chromosome
- 21
- Canonical length
- 376 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins, Predicted membrane proteins, Transporters
OverviewNCBI Gene
The protein encoded by this gene is an acyltransferase that converts lysophosphatidic acid into phosphatidic acid, which is the second step in the de novo phospholipid biosynthetic pathway. The encoded protein may be an integral membrane protein. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
376 residues, UniProt reviewed canonical sequence.
>Q9NRZ7|AGPAT3
1 MGLLAFLKTQ FVLHLLVGFV FVVSGLVINF VQLCTLALWP VSKQLYRRLN CRLAYSLWSQ
61 LVMLLEWWSC TECTLFTDQA TVERFGKEHA VIILNHNFEI DFLCGWTMCE RFGVLGSSKV
121 LAKKELLYVP LIGWTWYFLE IVFCKRKWEE DRDTVVEGLR RLSDYPEYMW FLLYCEGTRF
181 TETKHRVSME VAAAKGLPVL KYHLLPRTKG FTTAVKCLRG TVAAVYDVTL NFRGNKNPSL
241 LGILYGKKYE ADMCVRRFPL EDIPLDEKEA AQWLHKLYQE KDALQEIYNQ KGMFPGEQFK
301 PARRPWTLLN FLSWATILLS PLFSFVLGVF ASGSPLLILT FLGFVGAASF GVRRLIGVTE
361 IEKGSSYGNQ EFKKKELocalizationUniProt · AlphaFold · HPA
Whether an antibody against AGPAT3 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)
- 0.24
- Highest tissue expression
- 58 nTPM
Expression across tissuesHPA
Tissue
- retina: 58 nTPM
- skeletal muscle: 57 nTPM
- liver: 51 nTPM
- spinal cord: 50 nTPM
- kidney: 50 nTPM
- small intestine: 49 nTPM
Single-cell type
- rod photoreceptor cells: 323 nCPM
- early spermatids: 314 nCPM
- late spermatids: 293 nCPM
- cone photoreceptor cells: 255 nCPM
- proximal tubule cells: 239 nCPM
- myonuclei: 202 nCPM
Immune cell
- non-classical monocyte: 9.6 nTPM
- intermediate monocyte: 7.4 nTPM
- myeloid DC: 3.8 nTPM
- classical monocyte: 3.3 nTPM
- T-reg: 3 nTPM
- eosinophil: 2.2 nTPM
Brain region
- medulla oblongata: 131 nTPM
- thalamus: 124 nTPM
- spinal cord: 123 nTPM
- white matter: 119 nTPM
- basal ganglia: 118 nTPM
- cerebellum: 109 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about AGPAT3.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 48 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)
- 0.14
- gnomAD pLI
- 1
- gnomAD missense Z
- 2.54
- DepMap mean gene effect
- 0.05
- 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
- CDP-diacylglycerol biosynthetic process
- phosphatidic acid biosynthetic process
- phospholipid biosynthetic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads AGPAT3 as an antibody target. Whether an autoantibody or antibody against AGPAT3 could matter depends on whether native AGPAT3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
AGPAT3 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 AGPAT3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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