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Sulfate anion transporter 1 (SLC26A1)

Homo sapiens — UniProt Q9H2B4

Gene: SLC26A1Homo sapiensSwissProt reviewedTransporter

Data last refreshed: (UniProt release unknown)

Key facts

Sulfate anion transporter 1 (SLC26A1) is a protein from Homo sapiens identified by UniProt accession Q9H2B4, 701 residues long. MolForge cross-references it against 0 known binders and 148 disease associations.

  • UniProt accession: Q9H2B4; gene symbol SLC26A1.
  • Organism: Homo sapiens.
  • Length: 701 amino acids.
  • Target class: Transporter.
  • Top disease associations (Open Targets): nephrolithiasis susceptibility caused by SLC26A1, mucopolysaccharidosis type 1 and Hurler syndrome.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameSulfate anion transporter 1
UniProt accessionQ9H2B4
GeneSLC26A1
OrganismHomo sapiens
Length701 residues
Molecular weight—
EC numbers—
Target classTransporter (inferred from UniProt keywords / EC)
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 (148)

Diseases linked to this target (Open Targets).

  • nephrolithiasis susceptibility caused by SLC26A1 · score 0.62
  • mucopolysaccharidosis type 1 · score 0.57
  • Hurler syndrome · score 0.55
  • Hurler-Scheie syndrome · score 0.52
  • Scheie syndrome · score 0.51
  • nephrolithiasis · score 0.51
  • calcium oxalate urolithiasis · score 0.46
  • hypersulfaturia · score 0.45
  • Interstitial pneumonitis · score 0.34
  • mucopolysaccharidosis · score 0.34

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9H2B4-F1alphafoldPREDICTED82.65—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9H2B4.

Amino-acid sequence (701 residues)

MDESPEPLQQ GRGPVPVRRQ RPAPRGLREM LKARLWCSCS CSVLCVRALV QDLLPATRWL RQYRPREYLA GDVMSGLVIG IILVPQAIAY SLLAGLQPIY SLYTSFFANL IYFLMGTSRH VSVGIFSLLC LMVGQVVDRE LQLAGFDPSQ DGLQPGANSS TLNGSAAMLD CGRDCYAIRV ATALTLMTGL YQVLMGVLRL GFVSAYLSQP LLDGFAMGAS VTILTSQLKH LLGVRIPRHQ GPGMVVLTWL SLLRGAGQAN VCDVVTSTVC LAVLLAAKEL SDRYRHRLRV PLPTELLVIV VATLVSHFGQ LHKRFGSSVA GDIPTGFMPP QVPEPRLMQR VALDAVALAL VAAAFSISLA EMFARSHGYS VRANQELLAV GCCNVLPAFL HCFATSAALA KSLVKTATGC RTQLSSVVSA TVVLLVLLAL APLFHDLQRS VLACVIVVSL RGALRKVWDL PRLWRMSPAD ALVWAGTAAT CMLVSTEAGL LAGVILSLLS LAGRTQRPRT ALLARIGDTA FYEDATEFEG LVPEPGVRVF RFGGPLYYAN KDFFLQSLYS LTGLDAGCMA ARRKEGGSET GVGEGGPAQG EDLGPVSTRA ALVPAAAGFH TVVIDCAPLL FLDAAGVSTL QDLRRDYGAL GISLLLACCS PPVRDILSRG GFLGEGPGDT AEEEQLFLSV HDAVQTARAR HRELEATDAH L

Frequently asked questions

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

Which diseases are associated with SLC26A1?

The strongest Open Targets associations for SLC26A1 are nephrolithiasis susceptibility caused by SLC26A1, mucopolysaccharidosis type 1, Hurler syndrome, Hurler-Scheie syndrome and Scheie syndrome.

How long is the SLC26A1 protein?

The Homo sapiens SLC26A1 protein (UniProt Q9H2B4) is 701 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

UniProtQ9H2B4
GeneSLC26A1
OrganismHomo sapiens
Length701
Binders0
Diseases148
View on UniProt