QPCT
Glutaminyl-peptide cyclotransferase
Also known as: GCT, QC, QPCT_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q16769
- Gene
- QPCT
- Ensembl
- ENSG00000115828
- Chromosome
- 2
- Canonical length
- 361 aa
- Protein class
- Enzymes, Metabolic proteins, Plasma proteins, Predicted intracellular proteins, Predicted secreted proteins
- Subcellular location
- Cytosol
- Secretome location
- Secreted to blood
OverviewNCBI Gene
This gene encodes human pituitary glutaminyl cyclase, which is responsible for the presence of pyroglutamyl residues in many neuroendocrine peptides. The amino acid sequence of this enzyme is 86% identical to that of bovine glutaminyl cyclase. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
361 residues, UniProt reviewed canonical sequence.
>Q16769|QPCT
1 MAGGRHRRVV GTLHLLLLVA ALPWASRGVS PSASAWPEEK NYHQPAILNS SALRQIAEGT
61 SISEMWQNDL QPLLIERYPG SPGSYAARQH IMQRIQRLQA DWVLEIDTFL SQTPYGYRSF
121 SNIISTLNPT AKRHLVLACH YDSKYFSHWN NRVFVGATDS AVPCAMMLEL ARALDKKLLS
181 LKTVSDSKPD LSLQLIFFDG EEAFLHWSPQ DSLYGSRHLA AKMASTPHPP GARGTSQLHG
241 MDLLVLLDLI GAPNPTFPNF FPNSARWFER LQAIEHELHE LGLLKDHSLE GRYFQNYSYG
301 GVIQDDHIPF LRRGVPVLHL IPSPFPEVWH TMDDNEENLD ESTIDNLNKI LQVFVLEYLH
361 LLocalizationUniProt · AlphaFold · HPA
Whether an antibody against QPCT 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.27
- Highest tissue expression
- 162 nTPM
Expression across tissuesHPA
Tissue
- adrenal gland: 162 nTPM
- epididymis: 98 nTPM
- bone marrow: 45 nTPM
- hypothalamus: 35 nTPM
- skin: 34 nTPM
- pituitary gland: 26 nTPM
Single-cell type
- melanocytes: 857 nCPM
- neutrophils: 460 nCPM
- pancreatic islet cells: 281 nCPM
- decidual stromal cells: 129 nCPM
- neutrophil progenitors: 112 nCPM
- neuroendocrine cells: 106 nCPM
Immune cell
- neutrophil: 1,537 nTPM
- classical monocyte: 346 nTPM
- total PBMC: 170 nTPM
- myeloid DC: 125 nTPM
- intermediate monocyte: 39 nTPM
- basophil: 9.8 nTPM
Brain region
- hypothalamus: 52 nTPM
- pons: 24 nTPM
- midbrain: 17 nTPM
- cerebral cortex: 16 nTPM
- thalamus: 15 nTPM
- medulla oblongata: 14 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about QPCT.
Disease | ImmuneIEDB
Conditions an epitope on QPCT was assayed in.
- type 1 diabetes mellitus T 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)
- 1.53
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.94
- DepMap mean gene effect
- -0.03
- 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
- peptidyl-pyroglutamic acid biosynthetic process, using glutaminyl-peptide cyclotransferase
- protein modification process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads QPCT as an antibody target. Whether an autoantibody or antibody against QPCT could matter depends on whether native QPCT is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
QPCT is annotated as secreted, so native QPCT circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label QPCT as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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