Skip to content

Sphingomyelin phosphodiesterase (SMPD1)

Homo sapiens — UniProt P17405

Gene: SMPD1Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Sphingomyelin phosphodiesterase (SMPD1) is a protein from Homo sapiens identified by UniProt accession P17405, 631 residues long. MolForge cross-references it against 3 known binders and 350 disease associations.

  • UniProt accession: P17405; gene symbol SMPD1.
  • Organism: Homo sapiens.
  • Length: 631 amino acids.
  • Top disease associations (Open Targets): Niemann-Pick disease type A, Niemann-Pick disease type B and Niemann-Pick disease.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameSphingomyelin phosphodiesterase
UniProt accessionP17405
GeneSMPD1
OrganismHomo sapiens
Length631 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 (350)

Diseases linked to this target (Open Targets).

  • Niemann-Pick disease type A · score 0.86
  • Niemann-Pick disease type B · score 0.85
  • Niemann-Pick disease · score 0.58
  • neurodegenerative disease · score 0.53
  • Parkinson disease · score 0.52
  • lysosomal storage disease · score 0.52
  • multiple sclerosis · score 0.52
  • Alzheimer disease · score 0.52
  • genetic disorder · score 0.47
  • acid sphingomyelinase deficiency · score 0.46

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P17405-F1alphafoldPREDICTED88.02—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for P17405.

Amino-acid sequence (631 residues)

MPRYGASLRQ SCPRSGREQG QDGTAGAPGL LWMGLVLALA LALALALALS DSRVLWAPAE AHPLSPQGHP ARLHRIVPRL RDVFGWGNLT CPICKGLFTA INLGLKKEPN VARVGSVAIK LCNLLKIAPP AVCQSIVHLF EDDMVEVWRR SVLSPSEACG LLLGSTCGHW DIFSSWNISL PTVPKPPPKP PSPPAPGAPV SRILFLTDLH WDHDYLEGTD PDCADPLCCR RGSGLPPASR PGAGYWGEYS KCDLPLRTLE SLLSGLGPAG PFDMVYWTGD IPAHDVWHQT RQDQLRALTT VTALVRKFLG PVPVYPAVGN HESTPVNSFP PPFIEGNHSS RWLYEAMAKA WEPWLPAEAL RTLRIGGFYA LSPYPGLRLI SLNMNFCSRE NFWLLINSTD PAGQLQWLVG ELQAAEDRGD KVHIIGHIPP GHCLKSWSWN YYRIVARYEN TLAAQFFGHT HVDEFEVFYD EETLSRPLAV AFLAPSATTY IGLNPGYRVY QIDGNYSGSS HVVLDHETYI LNLTQANIPG AIPHWQLLYR ARETYGLPNT LPTAWHNLVY RMRGDMQLFQ TFWFLYHKGH PPSEPCGTPC RLATLCAQLS ARADSPALCR HLMPDGSLPE AQSLWPRPLF C

Frequently asked questions

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

Which diseases are associated with SMPD1?

The strongest Open Targets associations for SMPD1 are Niemann-Pick disease type A, Niemann-Pick disease type B, Niemann-Pick disease, neurodegenerative disease and Parkinson disease.

How long is the SMPD1 protein?

The Homo sapiens SMPD1 protein (UniProt P17405) is 631 amino acids long.

Browse: Targets: S · 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.

Explore Sphingomyelin phosphodiesterase with MolForge

Find binders, run structure-based screening, and map this target across diseases and approved drugs with our AI-powered platform.

Browse all targets

Quick facts

UniProtP17405
GeneSMPD1
OrganismHomo sapiens
Length631
Binders3
Diseases350
View on UniProt