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Protein sprouty homolog 1 (SPRY1)

Homo sapiens — UniProt O43609

Gene: SPRY1Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Protein sprouty homolog 1 (SPRY1) is a protein from Homo sapiens identified by UniProt accession O43609, 319 residues long. MolForge cross-references it against 0 known binders and 212 disease associations.

  • UniProt accession: O43609; gene symbol SPRY1.
  • Organism: Homo sapiens.
  • Length: 319 amino acids.
  • Top disease associations (Open Targets): neurodegenerative disease, heel bone mineral density and genetic disorder.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameProtein sprouty homolog 1
UniProt accessionO43609
GeneSPRY1
OrganismHomo sapiens
Length319 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 (212)

Diseases linked to this target (Open Targets).

  • neurodegenerative disease · score 0.37
  • heel bone mineral density · score 0.37
  • genetic disorder · score 0.27
  • FEV/FVC ratio · score 0.23
  • blood phosphate measurement · score 0.23
  • platelet count · score 0.23
  • hair shape measurement · score 0.23
  • Alzheimer disease · score 0.22
  • lysosomal storage disease · score 0.22
  • Parkinson disease · score 0.22

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-O43609-F1alphafoldPREDICTED62.10—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for O43609.

Amino-acid sequence (319 residues)

MDPQNQHGSG SSLVVIQQPS LDSRQRLDYE REIQPTAILS LDQIKAIRGS NEYTEGPSVV KRPAPRTAPR QEKHERTHEI IPINVNNNYE HRHTSHLGHA VLPSNARGPI LSRSTSTGSA ASSGSNSSAS SEQGLLGRSP PTRPVPGHRS ERAIRTQPKQ LIVDDLKGSL KEDLTQHKFI CEQCGKCKCG ECTAPRTLPS CLACNRQCLC SAESMVEYGT CMCLVKGIFY HCSNDDEGDS YSDNPCSCSQ SHCCSRYLCM GAMSLFLPCL LCYPPAKGCL KLCRRCYDWI HRPGCRCKNS NTVYCKLESC PSRGQGKPS

Frequently asked questions

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

Which diseases are associated with SPRY1?

The strongest Open Targets associations for SPRY1 are neurodegenerative disease, heel bone mineral density, genetic disorder, FEV/FVC ratio and blood phosphate measurement.

How long is the SPRY1 protein?

The Homo sapiens SPRY1 protein (UniProt O43609) is 319 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.

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Quick facts

UniProtO43609
GeneSPRY1
OrganismHomo sapiens
Length319
Binders0
Diseases212
View on UniProt