PADI2
Protein-arginine deiminase type-2
Also known as: KIAA0994, PADI2_HUMAN, PDI2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y2J8
- Gene
- PADI2
- Ensembl
- ENSG00000117115
- Chromosome
- 1
- Canonical length
- 665 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a member of the peptidyl arginine deiminase family of enzymes, which catalyze the post-translational deimination of proteins by converting arginine residues into citrullines in the presence of calcium ions. The family members have distinct substrate specificities and tissue-specific expression patterns. The type II enzyme is the most widely expressed family member. Known substrates for this enzyme include myelin basic protein in the central nervous system and vimentin in skeletal muscle and macrophages. This enzyme is thought to play a role in the onset and progression of neurodegenerative human disorders, including Alzheimer disease and multiple sclerosis, and it has also been implicated in glaucoma pathogenesis. This gene exists in a cluster with four other paralogous genes. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
665 residues, UniProt reviewed canonical sequence.
>Q9Y2J8|PADI2
1 MLRERTVRLQ YGSRVEAVYV LGTYLWTDVY SAAPAGAQTF SLKHSEHVWV EVVRDGEAEE
61 VATNGKQRWL LSPSTTLRVT MSQASTEASS DKVTVNYYDE EGSIPIDQAG LFLTAIEISL
121 DVDADRDGVV EKNNPKKASW TWGPEGQGAI LLVNCDRETP WLPKEDCRDE KVYSKEDLKD
181 MSQMILRTKG PDRLPAGYEI VLYISMSDSD KVGVFYVENP FFGQRYIHIL GRRKLYHVVK
241 YTGGSAELLF FVEGLCFPDE GFSGLVSIHV SLLEYMAQDI PLTPIFTDTV IFRIAPWIMT
301 PNILPPVSVF VCCMKDNYLF LKEVKNLVEK TNCELKVCFQ YLNRGDRWIQ DEIEFGYIEA
361 PHKGFPVVLD SPRDGNLKDF PVKELLGPDF GYVTREPLFE SVTSLDSFGN LEVSPPVTVN
421 GKTYPLGRIL IGSSFPLSGG RRMTKVVRDF LKAQQVQAPV ELYSDWLTVG HVDEFMSFVP
481 IPGTKKFLLL MASTSACYKL FREKQKDGHG EAIMFKGLGG MSSKRITINK ILSNESLVQE
541 NLYFQRCLDW NRDILKKELG LTEQDIIDLP ALFKMDEDHR ARAFFPNMVN MIVLDKDLGI
601 PKPFGPQVEE ECCLEMHVRG LLEPLGLECT FIDDISAYHK FLGEVHCGTN VRRKPFTFKW
661 WHMVPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PADI2 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)
- 0.23
- Highest tissue expression
- 460 nTPM
Expression across tissuesHPA
Tissue
- tongue: 460 nTPM
- skeletal muscle: 292 nTPM
- spinal cord: 236 nTPM
- midbrain: 125 nTPM
- rectum: 87 nTPM
- colon: 84 nTPM
Single-cell type
- cone photoreceptor cells: 232 nCPM
- myonuclei: 231 nCPM
- colonocytes: 226 nCPM
- neutrophils: 219 nCPM
- microglia: 202 nCPM
- oligodendrocytes: 162 nCPM
Immune cell
- neutrophil: 101 nTPM
- eosinophil: 43 nTPM
- classical monocyte: 16 nTPM
- myeloid DC: 12 nTPM
- total PBMC: 6.4 nTPM
- basophil: 1.3 nTPM
Brain region
- white matter: 478 nTPM
- medulla oblongata: 414 nTPM
- spinal cord: 374 nTPM
- midbrain: 319 nTPM
- pons: 318 nTPM
- hypothalamus: 318 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about PADI2.
Disease | ImmuneIEDB
Conditions an epitope on PADI2 was assayed in.
- rheumatoid arthritis 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)
- 0.89
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.49
- DepMap mean gene effect
- 0
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cellular response to leukemia inhibitory factor
- chromatin remodeling
- estrogen receptor signaling pathway
- negative regulation of chemokine-mediated signaling pathway
- substantia nigra development
- transcription initiation-coupled chromatin remodeling
- negative regulation of lymphocyte chemotaxis
Molecular functions
- calcium ion binding
- histone arginine deiminase activity
- histone H3R26 arginine deiminase activity
- nuclear estrogen receptor binding
- protein homodimerization activity
- protein-arginine deiminase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Protein-arginine deiminase
- Cupredoxin
- Protein-arginine deiminase, C-terminal
- Protein-arginine deiminase (PAD), N-terminal
- Protein-arginine deiminase (PAD), central domain
- Protein-arginine deiminase, central domain superfamily
- PAD, N-terminal domain superfamily
- Protein-arginine deiminase (PAD)
- Protein-arginine deiminase (PAD) N-terminal domain
- Protein-arginine deiminase (PAD) middle domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PADI2 as an antibody target. Whether an autoantibody or antibody against PADI2 could matter depends on whether native PADI2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PADI2 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 PADI2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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