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Multiple inositol polyphosphate phosphatase 1 (MINPP1)

Homo sapiens — UniProt Q9UNW1

Gene: MINPP1Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Multiple inositol polyphosphate phosphatase 1 (MINPP1) is a protein from Homo sapiens identified by UniProt accession Q9UNW1, 487 residues long. MolForge cross-references it against 0 known binders and 40 disease associations.

  • UniProt accession: Q9UNW1; gene symbol MINPP1.
  • Organism: Homo sapiens.
  • Length: 487 amino acids.
  • Top disease associations (Open Targets): pontocerebellar hypoplasia, follicular thyroid carcinoma and neurodegenerative disease.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameMultiple inositol polyphosphate phosphatase 1
UniProt accessionQ9UNW1
GeneMINPP1
OrganismHomo sapiens
Length487 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 (40)

Diseases linked to this target (Open Targets).

  • pontocerebellar hypoplasia · score 0.61
  • follicular thyroid carcinoma · score 0.58
  • neurodegenerative disease · score 0.42
  • pontocerebellar hypoplasia type 7 · score 0.37
  • Non-syndromic pontocerebellar hypoplasia · score 0.34
  • blood protein measurement · score 0.34
  • follicular thyroid adenoma · score 0.33
  • hepatocellular carcinoma · score 0.08
  • neoplasm · score 0.03
  • glioblastoma · score 0.02

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9UNW1-F1alphafoldPREDICTED89.52—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9UNW1.

Amino-acid sequence (487 residues)

MLRAPGCLLR TSVAPAAALA AALLSSLARC SLLEPRDPVA SSLSPYFGTK TRYEDVNPVL LSGPEAPWRD PELLEGTCTP VQLVALIRHG TRYPTVKQIR KLRQLHGLLQ ARGSRDGGAS STGSRDLGAA LADWPLWYAD WMDGQLVEKG RQDMRQLALR LASLFPALFS RENYGRLRLI TSSKHRCMDS SAAFLQGLWQ HYHPGLPPPD VADMEFGPPT VNDKLMRFFD HCEKFLTEVE KNATALYHVE AFKTGPEMQN ILKKVAATLQ VPVNDLNADL IQVAFFTCSF DLAIKGVKSP WCDVFDIDDA KVLEYLNDLK QYWKRGYGYT INSRSSCTLF QDIFQHLDKA VEQKQRSQPI SSPVILQFGH AETLLPLLSL MGYFKDKEPL TAYNYKKQMH RKFRSGLIVP YASNLIFVLY HCENAKTPKE QFRVQMLLNE KVLPLAYSQE TVSFYEDLKN HYKDILQSCQ TSEECELARA NSTSDEL

Frequently asked questions

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

Which diseases are associated with MINPP1?

The strongest Open Targets associations for MINPP1 are pontocerebellar hypoplasia, follicular thyroid carcinoma, neurodegenerative disease, pontocerebellar hypoplasia type 7 and Non-syndromic pontocerebellar hypoplasia.

How long is the MINPP1 protein?

The Homo sapiens MINPP1 protein (UniProt Q9UNW1) is 487 amino acids long.

Browse: Targets: M · 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

UniProtQ9UNW1
GeneMINPP1
OrganismHomo sapiens
Length487
Binders0
Diseases40
View on UniProt