Mitochondrial import receptor subunit TOM22 homolog (TOMM22)

Homo sapiens — UniProt Q9NS69

Gene: TOMM22Homo sapiensSwissProt reviewed

About Mitochondrial import receptor subunit TOM22 homolog

Mitochondrial import receptor subunit TOM22 homolog (TOMM22) is a protein from Homo sapiens identified by UniProt accession Q9NS69, 142 residues long. MolForge cross-references it against 0 known binders and 91 disease associations.

Target properties

Protein nameMitochondrial import receptor subunit TOM22 homolog
UniProt accessionQ9NS69
GeneTOMM22
OrganismHomo sapiens
Length142 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 (91)

Diseases linked to this target (Open Targets).

  • triglyceride measurement · score 0.09
  • Blackfan-Diamond anemia · score 0.08
  • hereditary persistence of fetal hemoglobin-sickle cell disease syndrome · score 0.08
  • alpha thalassemia-intellectual disability syndrome type 1 · score 0.07
  • Alpha-thalassemia - intellectual disability syndrome linked to chromosome 16 · score 0.07
  • delta-beta-thalassemia · score 0.06
  • hemoglobin D disease · score 0.06
  • hemoglobin E-beta-thalassemia syndrome · score 0.06
  • Alpha-thalassemia · score 0.05
  • Beta-thalassemia · score 0.05

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9NS69-F1alphafoldPREDICTED71.15—

Amino-acid sequence (142 residues)

MAAAVAAAGA GEPQSPDELL PKGDAEKPEE ELEEDDDEEL DETLSERLWG LTEMFPERVR SAAGATFDLS LFVAQKMYRF SRAALWIGTT SFMILVLPVV FETEKLQMEQ QQQLQQRQIL LGPNTGLSGG MPGALPSLPG KI

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Quick facts

UniProtQ9NS69
GeneTOMM22
OrganismHomo sapiens
Length142
Binders0
Diseases91
View on UniProt