GPAT3
Glycerol-3-phosphate acyltransferase 3
Also known as: AGPAT10, AGPAT9, GPAT3_HUMAN, HMFN0839, LPAAT-theta, MAG1, MGC11324
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q53EU6
- Gene
- GPAT3
- Ensembl
- ENSG00000138678
- Chromosome
- 4
- Canonical length
- 434 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted membrane proteins
OverviewNCBI Gene
This gene encodes a member of the lysophosphatidic acid acyltransferase protein family. The encoded protein is an enzyme which catalyzes the conversion of glycerol-3-phosphate to lysophosphatidic acid in the synthesis of triacylglycerol. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jan 2012]
Canonical amino-acid sequenceUniProt
434 residues, UniProt reviewed canonical sequence.
>Q53EU6|GPAT3
1 MEGAELAGKI LSTWLTLVLG FILLPSVFGV SLGISEIYMK ILVKTLEWAT IRIEKGTPKE
61 SILKNSASVG IIQRDESPME KGLSGLRGRD FELSDVFYFS KKGLEAIVED EVTQRFSSEE
121 LVSWNLLTRT NVNFQYISLR LTMVWVLGVI VRYCVLLPLR VTLAFIGISL LVIGTTLVGQ
181 LPDSSLKNWL SELVHLTCCR ICVRALSGTI HYHNKQYRPQ KGGICVANHT SPIDVLILTT
241 DGCYAMVGQV HGGLMGIIQR AMVKACPHVW FERSEMKDRH LVTKRLKEHI ADKKKLPILI
301 FPEGTCINNT SVMMFKKGSF EIGGTIHPVA IKYNPQFGDA FWNSSKYNMV SYLLRMMTSW
361 AIVCDVWYMP PMTREEGEDA VQFANRVKSA IAIQGGLTEL PWDGGLKRAK VKDIFKEEQQ
421 KNYSKMIVGN GSLSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GPAT3 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)
- 0.29
- Highest tissue expression
- 83 nTPM
Expression across tissuesHPA
Tissue
- kidney: 83 nTPM
- duodenum: 38 nTPM
- skeletal muscle: 36 nTPM
- small intestine: 34 nTPM
- heart muscle: 24 nTPM
- parathyroid gland: 22 nTPM
Single-cell type
- cdc: 787 nCPM
- renal collecting duct intercalated cells: 731 nCPM
- distal convoluted tubule cells: 398 nCPM
- mast cells: 332 nCPM
- neutrophils: 315 nCPM
- cardiomyocytes: 281 nCPM
Immune cell
- basophil: 183 nTPM
- neutrophil: 91 nTPM
- myeloid DC: 81 nTPM
- classical monocyte: 33 nTPM
- intermediate monocyte: 28 nTPM
- non-classical monocyte: 24 nTPM
Brain region
- choroid plexus: 20 nTPM
- pons: 12 nTPM
- medulla oblongata: 9.1 nTPM
- cerebellum: 8.1 nTPM
- midbrain: 6.9 nTPM
- cerebral cortex: 6 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)
- 1.11
- gnomAD pLI
- 0
- DepMap mean gene effect
- 0
- 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
- CDP-diacylglycerol biosynthetic process
- glycerol-3-phosphate metabolic process
- phosphatidic acid biosynthetic process
- regulation of TOR signaling
- triglyceride biosynthetic process
Molecular functions
- 1-acylglycerol-3-phosphate O-acyltransferase activity
- glycerol-3-phosphate O-acyltransferase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of GPAT3 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 GPAT3 as an antibody target. Whether an autoantibody or antibody against GPAT3 could matter depends on whether native GPAT3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GPAT3 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 GPAT3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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