GPKOW
G-patch domain and KOW motifs-containing protein
Also known as: GPATC5, GPATCH5, GPKOW_HUMAN, Mos2, Spp2, T54
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q92917
- Gene
- GPKOW
- Ensembl
- ENSG00000068394
- Chromosome
- X
- Canonical length
- 476 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
This gene encodes a putative RNA-binding protein containing G-patch and KOW (Kyprides, Ouzounis, Woese) domains. The encoded protein interacts directly with protein kinase A and protein kinase X and is also found associated with the spliceosome. [provided by RefSeq, Aug 2013]
Canonical amino-acid sequenceUniProt
476 residues, UniProt reviewed canonical sequence.
>Q92917|GPKOW
1 MADSKEGVLP LTAASTAPIS FGFTRTSARR RLADSGDGAG PSPEEKDFLK TVEGRELQSV
61 KPQEAPKELV IPLIQNGHRR QPPARPPGPS TDTGALADGV VSQAVKELIA ESKKSLEERE
121 NAGVDPTLAI PMIQKGCTPS GEGADSEPRA ETVPEEANYE AVPVEAYGLA MLRGMGWKPG
181 EGIGRTFNQV VKPRVNSLRP KGLGLGANLT EAQALTPTGP SRMPRPDEEQ EKDKEDQPQG
241 LVPGGAVVVL SGPHRGLYGK VEGLDPDNVR AMVRLAVGSR VVTVSEYYLR PVSQQEFDKN
301 TLDLRQQNGT ASSRKTLWNQ ELYIQQDNSE RKRKHLPDRQ DGPAAKSEKA APRSQHWLHR
361 DLRVRFVDNM YKGGQYYNTK MIIEDVLSPD TCVCRTDEGR VLEGLREDML ETLVPKAEGD
421 RVMVVLGPQT GRVGHLLSRD RARSRALVQL PRENQVVELH YDAICQYMGP SDTDDDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GPKOW 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)
- 0.51
- Highest tissue expression
- 35 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 35 nTPM
- midbrain: 26 nTPM
- tongue: 24 nTPM
- choroid plexus: 23 nTPM
- spinal cord: 23 nTPM
- blood vessel: 23 nTPM
Single-cell type
- oocytes: 60 nCPM
- syncytiotrophoblasts: 54 nCPM
- esophageal apical cells: 42 nCPM
- cytotrophoblasts: 34 nCPM
- decidual stromal cells: 27 nCPM
- esophageal suprabasal cells: 27 nCPM
Immune cell
- gdT-cell: 37 nTPM
- non-classical monocyte: 36 nTPM
- naive B-cell: 35 nTPM
- intermediate monocyte: 31 nTPM
- T-reg: 31 nTPM
- MAIT T-cell: 30 nTPM
Brain region
- thalamus: 41 nTPM
- medulla oblongata: 38 nTPM
- midbrain: 37 nTPM
- white matter: 37 nTPM
- cerebellum: 34 nTPM
- spinal cord: 34 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)
- 0.19
- gnomAD pLI
- 1
- gnomAD missense Z
- 0.92
- DepMap mean gene effect
- -1.02
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- via spliceosome
- mRNA splicing
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- G-patch domain
- KOW
- Large ribosomal subunit protein uL2, domain 2
- KOW motif
- Spp2/MOS2, G-patch domain
- G-patch domain and KOW motifs-containing protein, KOW 1
- G-patch domain and KOW motifs-containing protein, KOW 2
- Pre-mRNA-splicing factor Spp2-like
- G-patch domain
- GPKOW C-terminal domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of GPKOW 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 GPKOW as an antibody target. Whether an autoantibody or antibody against GPKOW could matter depends on whether native GPKOW is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GPKOW 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 GPKOW as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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