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Omega-hydroxyceramide transacylase (PNPLA1)

Homo sapiens — UniProt Q8N8W4

Gene: PNPLA1Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Omega-hydroxyceramide transacylase (PNPLA1) is a protein from Homo sapiens identified by UniProt accession Q8N8W4, 532 residues long. MolForge cross-references it against 0 known binders and 77 disease associations.

  • UniProt accession: Q8N8W4; gene symbol PNPLA1.
  • Organism: Homo sapiens.
  • Length: 532 amino acids.
  • Top disease associations (Open Targets): congenital non-bullous ichthyosiform erythroderma, congenital reticular ichthyosiform erythroderma and inherited ichthyosis.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameOmega-hydroxyceramide transacylase
UniProt accessionQ8N8W4
GenePNPLA1
OrganismHomo sapiens
Length532 residues
Molecular weight—
EC numbers—
Target class—
Subcellular location—
Keywords—

Druggability

Target tractability assessment (Open Targets + pocket analysis). No approved drug

Druggability tierMEDIUM
Druggability score—
Pocket score—
Max clinical phase—

Disease associations (77)

Diseases linked to this target (Open Targets).

  • congenital non-bullous ichthyosiform erythroderma · score 0.68
  • congenital reticular ichthyosiform erythroderma · score 0.53
  • inherited ichthyosis · score 0.46
  • autosomal recessive congenital ichthyosis · score 0.38
  • lamellar ichthyosis · score 0.37
  • body height · score 0.36
  • ichthyosis · score 0.34
  • hematocrit · score 0.31
  • red blood cell density measurement · score 0.30
  • erythrocyte count · score 0.30

3D Structure (1)

Experimental (PDB) and predicted (AlphaFold) structures for this protein.

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q8N8W4-F1alphafoldPREDICTED63.77—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q8N8W4.

Amino-acid sequence (532 residues)

MEEQVFKGDP DTPHSISFSG SGFLSFYQAG AVDALRDLAP RMLETAHRFA GTSAGAVIAA LAICGIEMDE YLRVLNVGVA EVKKSFLGPL SPSCKMVQMM RQFLYRVLPE DSYKVTTGKL HVSLTRLTDG ENVVVSEFTS KEELIEALYC SCFVPVYCGL IPPTYRGVRY IDGGFTGMQP CAFWTDAITI STFSGQQDIC PRDCPAIFHD FRMFNCSFQF SLENIARMTH ALFPPDLVIL HDYYYRGYED AVLYLRRLNA VYLNSSSKRV IFPRVEVYCQ IELALGNECP ERSQPSLRAR QASLEGATQP HKEWVPKGDG RGSHGPPVSQ PVQTLEFTCE SPVSAPVSPL EQPPAQPLAS STPLSLSGMP PVSFPAVHKP PSSTPGSSLP TPPPGLSPLS PQQQVQPSGS PARSLHSQAP TSPRPSLGPS TVGAPQTLPR SSLSAFPAQP PVEELGQEQP QAVALLVSSK PKSAVPLVHV KETVSKPYVT ESPAEDSNWV NKVFKKNKQK TSGTRKGFPR HSGSKKPSSK VQ

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

Which diseases are associated with PNPLA1?

The strongest Open Targets associations for PNPLA1 are congenital non-bullous ichthyosiform erythroderma, congenital reticular ichthyosiform erythroderma, inherited ichthyosis, autosomal recessive congenital ichthyosis and lamellar ichthyosis.

How long is the PNPLA1 protein?

The Homo sapiens PNPLA1 protein (UniProt Q8N8W4) is 532 amino acids long.

Browse: Targets: P · all protein targets A–Z · drugs A–Z.

Sources

How this page is built: methodology · editorial policy & corrections.

For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

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Quick facts

UniProtQ8N8W4
GenePNPLA1
OrganismHomo sapiens
Length532
Binders0
Diseases77
View on UniProt