Seroatlas · Human Serome Atlas

PPAT

Amidophosphoribosyltransferase

Also known as: GPAT, PRAT, PUR1_HUMAN

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q06203
Gene
PPAT
Ensembl
ENSG00000128059
Chromosome
4
Canonical length
517 aa
Protein class
Enzymes, Metabolic proteins, Predicted intracellular proteins
Subcellular location
Midbody ring
Quaternary structure
Homotetramer

OverviewNCBI Gene

The protein encoded by this gene is a member of the purine/pyrimidine phosphoribosyltransferase family. It is a regulatory allosteric enzyme that catalyzes the first step of de novo purine nucleotide biosythetic pathway. This gene and PAICS/AIRC gene, a bifunctional enzyme catalyzing steps six and seven of this pathway, are located in close proximity on chromosome 4, and divergently transcribed from an intergenic region. [provided by RefSeq, Mar 2011]

Canonical amino-acid sequenceUniProt

517 residues, UniProt reviewed canonical sequence.

>Q06203|PPAT
     1  MELEELGIRE ECGVFGCIAS GEWPTQLDVP HVITLGLVGL QHRGQESAGI VTSDGSSVPT
    61  FKSHKGMGLV NHVFTEDNLK KLYVSNLGIG HTRYATTGKC ELENCQPFVV ETLHGKIAVA
   121  HNGELVNAAR LRKKLLRHGI GLSTSSDSEM ITQLLAYTPP QEQDDTPDWV ARIKNLMKEA
   181  PTAYSLLIMH RDVIYAVRDP YGNRPLCIGR LIPVSDINDK EKKTSETEGW VVSSESCSFL
   241  SIGARYYREV LPGEIVEISR HNVQTLDIIS RSEGNPVAFC IFEYVYFARP DSMFEDQMVY
   301  TVRYRCGQQL AIEAPVDADL VSTVPESATP AALAYAGKCG LPYVEVLCKN RYVGRTFIQP
   361  NMRLRQLGVA KKFGVLSDNF KGKRIVLVDD SIVRGNTISP IIKLLKESGA KEVHIRVASP
   421  PIKYPCFMGI NIPTKEELIA NKPEFDHLAE YLGANSVVYL SVEGLVSSVQ EGIKFKKQKE
   481  KKHDIMIQEN GNGLECFEKS GHCTACLTGK YPVELEW

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against PPAT 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)
0.24
Highest tissue expression
8.1 nTPM

Expression across tissuesHPA

Tissue

  • testis: 8.1 nTPM
  • lymph node: 7.8 nTPM
  • thymus: 7.7 nTPM
  • tonsil: 7.5 nTPM
  • breast: 6.7 nTPM
  • ovary: 6.7 nTPM

Single-cell type

  • erythrocyte progenitors: 69 nCPM
  • oocytes: 51 nCPM
  • cardiomyocytes: 50 nCPM
  • sertoli cells: 49 nCPM
  • cytotrophoblasts: 48 nCPM
  • differentiating spermatogonia: 48 nCPM

Immune cell

  • NK-cell: 10 nTPM
  • naive CD4 T-cell: 7.8 nTPM
  • memory B-cell: 7.5 nTPM
  • naive CD8 T-cell: 7.1 nTPM
  • naive B-cell: 6.2 nTPM
  • MAIT T-cell: 5.9 nTPM

Brain region

  • pons: 7.1 nTPM
  • white matter: 6.7 nTPM
  • hypothalamus: 6.6 nTPM
  • cerebral cortex: 6.5 nTPM
  • midbrain: 6.5 nTPM
  • thalamus: 6.5 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)
0.3
gnomAD pLI
0.99
gnomAD missense Z
3.06
DepMap mean gene effect
-0.71
DepMap dependency class
common

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

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of PPAT 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 PPAT as an antibody target. Whether an autoantibody or antibody against PPAT could matter depends on whether native PPAT is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

PPAT 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 PPAT as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/PPAT. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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