Hemoglobin subunit gamma-1 (HBG1)

Homo sapiens — UniProt P69891

Gene: HBG1Homo sapiensSwissProt reviewed

About Hemoglobin subunit gamma-1

Hemoglobin subunit gamma-1 (HBG1) is a protein from Homo sapiens identified by UniProt accession P69891, 147 residues long. MolForge cross-references it against 0 known binders and 39 disease associations.

Target properties

Protein nameHemoglobin subunit gamma-1
UniProt accessionP69891
GeneHBG1
OrganismHomo sapiens
Length147 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 (39)

Diseases linked to this target (Open Targets).

  • Hereditary persistence of fetal hemoglobin - beta-thalassemia · score 0.51
  • hereditary persistence of fetal hemoglobin-sickle cell disease syndrome · score 0.46
  • hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome · score 0.37
  • delta-beta-thalassemia · score 0.37
  • Red cell distribution width · score 0.18
  • hemoglobin E disease · score 0.14
  • blood protein measurement · score 0.10
  • reticulocyte count · score 0.07
  • PHF-tau measurement · score 0.06
  • fetal hemoglobin measurement · score 0.05

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P69891-F1alphafoldPREDICTED96.86—

Amino-acid sequence (147 residues)

MGHFTEEDKA TITSLWGKVN VEDAGGETLG RLLVVYPWTQ RFFDSFGNLS SASAIMGNPK VKAHGKKVLT SLGDATKHLD DLKGTFAQLS ELHCDKLHVD PENFKLLGNV LVTVLAIHFG KEFTPEVQAS WQKMVTAVAS ALSSRYH

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Quick facts

UniProtP69891
GeneHBG1
OrganismHomo sapiens
Length147
Binders0
Diseases39
View on UniProt