PRMT3
Protein arginine N-methyltransferase 3
Also known as: ANM3_HUMAN, HRMT1L3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O60678
- Gene
- PRMT3
- Ensembl
- ENSG00000185238
- Chromosome
- 11
- Canonical length
- 531 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene belongs to the protein arginine methyltransferase (PRMT) family. The encoded enzyme catalyzes the methylation of guanidino nitrogens of arginyl residues of proteins. The enzyme acts on 40S ribosomal protein S2 (rpS2), which is its major in-vivo substrate, and is involved in the proper maturation of the 80S ribosome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]
Canonical amino-acid sequenceUniProt
531 residues, UniProt reviewed canonical sequence.
>O60678|PRMT3
1 MCSLASGATG GRGAVENEED LPELSDSGDE AAWEDEDDAD LPHGKQQTPC LFCNRLFTSA
61 EETFSHCKSE HQFNIDSMVH KHGLEFYGYI KLINFIRLKN PTVEYMNSIY NPVPWEKEEY
121 LKPVLEDDLL LQFDVEDLYE PVSVPFSYPN GLSENTSVVE KLKHMEARAL SAEAALARAR
181 EDLQKMKQFA QDFVMHTDVR TCSSSTSVIA DLQEDEDGVY FSSYGHYGIH EEMLKDKIRT
241 ESYRDFIYQN PHIFKDKVVL DVGCGTGILS MFAAKAGAKK VLGVDQSEIL YQAMDIIRLN
301 KLEDTITLIK GKIEEVHLPV EKVDVIISEW MGYFLLFESM LDSVLYAKNK YLAKGGSVYP
361 DICTISLVAV SDVNKHADRI AFWDDVYGFK MSCMKKAVIP EAVVEVLDPK TLISEPCGIK
421 HIDCHTTSIS DLEFSSDFTL KITRTSMCTA IAGYFDIYFE KNCHNRVVFS TGPQSTKTHW
481 KQTVFLLEKP FSVKAGEALK GKVTVHKNKK DPRSLTVTLT LNNSTQTYGL QLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PRMT3 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)
- 0.33
- Highest tissue expression
- 19 nTPM
Expression across tissuesHPA
Tissue
- thyroid gland: 19 nTPM
- parathyroid gland: 10 nTPM
- skeletal muscle: 10 nTPM
- heart muscle: 9.1 nTPM
- thymus: 9.1 nTPM
- breast: 8.9 nTPM
Single-cell type
- megakaryocyte-erythroid progenitors: 134 nCPM
- erythrocyte progenitors: 101 nCPM
- lactotrophs: 88 nCPM
- pituitary stem cells: 88 nCPM
- choroid plexus epithelial cells: 82 nCPM
- megakaryocyte progenitors: 78 nCPM
Immune cell
- NK-cell: 11 nTPM
- myeloid DC: 9.9 nTPM
- MAIT T-cell: 7.7 nTPM
- intermediate monocyte: 6.1 nTPM
- naive CD4 T-cell: 6.1 nTPM
- memory CD4 T-cell: 5.5 nTPM
Brain region
- white matter: 16 nTPM
- medulla oblongata: 11 nTPM
- basal ganglia: 11 nTPM
- hypothalamus: 11 nTPM
- pons: 11 nTPM
- hippocampal formation: 11 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about PRMT3.
Disease | ImmuneIEDB
Conditions an epitope on PRMT3 was assayed in.
- narcolepsy B cell
- multiple sclerosis B cell
- peripheral nervous system disease B cell
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
- 0.11
- DepMap dependency class
- none
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
- chromatin remodeling
- methylation
- negative regulation of protein ubiquitination
- negative regulation of retinoic acid biosynthetic process
- positive regulation of osteoblast differentiation
- regulation of DNA-templated transcription
- transcription initiation-coupled chromatin remodeling
Molecular functions
- histone H4R3 methyltransferase activity
- histone methyltransferase activity
- methyltransferase activity
- protein-arginine N-methyltransferase activity
- protein-arginine omega-N asymmetric methyltransferase activity
- protein-arginine omega-N monomethyltransferase activity
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Zinc finger C2H2-type
- Protein arginine N-methyltransferase
- S-adenosyl-L-methionine-dependent methyltransferase superfamily
- Zinc finger C2H2 superfamily
- Protein arginine N-methyltransferase domain
- Ribosomal protein L11 methyltransferase (PrmA)
- Arginine methyltransferase oligomerization subdomain
- Protein arginine N-methyltransferase 3, C2H2 zinc finger
- Protein arginine N-methyltransferase 3-like, C2H2 zinc finger domain
- Protein arginine N-methyltransferase 3, C2H2 zinc finger domain
- Protein arginine N-methyltransferase 3, C2H2 zinc finger
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PRMT3 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 PRMT3 as an antibody target. Whether an autoantibody or antibody against PRMT3 could matter depends on whether native PRMT3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PRMT3 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 PRMT3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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