Syntaxin-1B (STX1B)

Homo sapiens — UniProt P61266

Gene: STX1BHomo sapiensSwissProt reviewed

About Syntaxin-1B

Syntaxin-1B (STX1B) is a protein from Homo sapiens identified by UniProt accession P61266, 288 residues long. MolForge cross-references it against 0 known binders and 120 disease associations.

Target properties

Protein nameSyntaxin-1B
UniProt accessionP61266
GeneSTX1B
OrganismHomo sapiens
Length288 residues
Molecular weight—
EC numbers—
Target classUNCLASSIFIED
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 (120)

Diseases linked to this target (Open Targets).

  • Generalized epilepsy with febrile seizures-plus · score 0.79
  • genetic disorder · score 0.47
  • generalized epilepsy with febrile seizures plus · score 0.45
  • Neurodevelopmental disorder · score 0.37
  • botulism · score 0.37
  • Epileptic encephalopathy · score 0.27
  • body mass index · score 0.20
  • lean body mass · score 0.20
  • fat body mass · score 0.18
  • body fat percentage · score 0.18

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P61266-F1alphafoldPREDICTED84.12—

Amino-acid sequence (288 residues)

MKDRTQELRS AKDSDDEEEV VHVDRDHFMD EFFEQVEEIR GCIEKLSEDV EQVKKQHSAI LAAPNPDEKT KQELEDLTAD IKKTANKVRS KLKAIEQSIE QEEGLNRSSA DLRIRKTQHS TLSRKFVEVM TEYNATQSKY RDRCKDRIQR QLEITGRTTT NEELEDMLES GKLAIFTDDI KMDSQMTKQA LNEIETRHNE IIKLETSIRE LHDMFVDMAM LVESQGEMID RIEYNVEHSV DYVERAVSDT KKAVKYQSKA RRKKIMIIIC CVVLGVVLAS SIGGTLGL

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Quick facts

UniProtP61266
GeneSTX1B
OrganismHomo sapiens
Length288
Binders0
Diseases120
View on UniProt