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Aspartyl aminopeptidase (DNPEP)

Homo sapiens — UniProt Q9ULA0

Gene: DNPEPHomo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Aspartyl aminopeptidase (DNPEP) is a protein from Homo sapiens identified by UniProt accession Q9ULA0, 485 residues long. MolForge cross-references it against 0 known binders and 38 disease associations.

  • UniProt accession: Q9ULA0; gene symbol DNPEP.
  • Organism: Homo sapiens.
  • Length: 485 amino acids.
  • Top disease associations (Open Targets): neurodegenerative disease, lysosomal storage disease and multiple sclerosis.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameAspartyl aminopeptidase
UniProt accessionQ9ULA0
GeneDNPEP
OrganismHomo sapiens
Length485 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 (38)

Diseases linked to this target (Open Targets).

  • neurodegenerative disease · score 0.43
  • lysosomal storage disease · score 0.36
  • multiple sclerosis · score 0.36
  • Alzheimer disease · score 0.36
  • Parkinson disease · score 0.36
  • neuroinflammatory disorder · score 0.14
  • acute myeloid leukemia · score 0.09
  • myelodysplastic syndrome · score 0.07
  • thrombocytopenia 4 · score 0.05
  • macrothrombocytopenia, isolated, 2, autosomal dominant · score 0.05

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9ULA0-F1alphafoldPREDICTED95.66—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9ULA0.

Amino-acid sequence (485 residues)

MSGHSPTRGA MQVAMNGKAR KEAVQTAAKE LLKFVNRSPS PFHAVAECRN RLLQAGFSEL KETEKWNIKP ESKYFMTRNS STIIAFAVGG QYVPGNGFSL IGAHTDSPCL RVKRRSRRSQ VGFQQVGVET YGGGIWSTWF DRDLTLAGRV IVKCPTSGRL EQQLVHVERP ILRIPHLAIH LQRNINENFG PNTEMHLVPI LATAIQEELE KGTPEPGPLN AVDERHHSVL MSLLCAHLGL SPKDIVEMEL CLADTQPAVL GGAYDEFIFA PRLDNLHSCF CALQALIDSC AGPGSLATEP HVRMVTLYDN EEVGSESAQG AQSLLTELVL RRISASCQHP TAFEEAIPKS FMISADMAHA VHPNYLDKHE ENHRPLFHKG PVIKVNSKQR YASNAVSEAL IREVANKVKV PLQDLMVRND TPCGTTIGPI LASRLGLRVL DLGSPQLAMH SIREMACTTG VLQTLTLFKG FFELFPSLSH NLLVD

Frequently asked questions

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

Which diseases are associated with DNPEP?

The strongest Open Targets associations for DNPEP are neurodegenerative disease, lysosomal storage disease, multiple sclerosis, Alzheimer disease and Parkinson disease.

How long is the DNPEP protein?

The Homo sapiens DNPEP protein (UniProt Q9ULA0) is 485 amino acids long.

Browse: Targets: D · 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

UniProtQ9ULA0
GeneDNPEP
OrganismHomo sapiens
Length485
Binders0
Diseases38
View on UniProt