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Translation initiation factor eIF2B subunit gamma (EIF2B3)

Homo sapiens — UniProt Q9NR50

Gene: EIF2B3Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Translation initiation factor eIF2B subunit gamma (EIF2B3) is a protein from Homo sapiens identified by UniProt accession Q9NR50, 452 residues long. MolForge cross-references it against 0 known binders and 61 disease associations.

  • UniProt accession: Q9NR50; gene symbol EIF2B3.
  • Organism: Homo sapiens.
  • Length: 452 amino acids.
  • Top disease associations (Open Targets): CACH syndrome, leukoencephalopathy with vanishing white matter and leukoencephalopathy with vanishing white matter 1.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameTranslation initiation factor eIF2B subunit gamma
UniProt accessionQ9NR50
GeneEIF2B3
OrganismHomo sapiens
Length452 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 (61)

Diseases linked to this target (Open Targets).

  • CACH syndrome · score 0.62
  • leukoencephalopathy with vanishing white matter · score 0.56
  • leukoencephalopathy with vanishing white matter 1 · score 0.44
  • ovarioleukodystrophy · score 0.37
  • late infantile CACH syndrome · score 0.37
  • congenital or early infantile CACH syndrome · score 0.37
  • juvenile or adult CACH syndrome · score 0.37
  • genetic disorder · score 0.19
  • platelet component distribution width · score 0.11
  • Blackfan-Diamond anemia · score 0.08

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9NR50-F1alphafoldPREDICTED72.53—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9NR50.

Amino-acid sequence (452 residues)

MEFQAVVMAV GGGSRMTDLT SSIPKPLLPV GNKPLIWYPL NLLERVGFEE VIVVTTRDVQ KALCAEFKMK MKPDIVCIPD DADMGTADSL RYIYPKLKTD VLVLSCDLIT DVALHEVVDL FRAYDASLAM LMRKGQDSIE PVPGQKGKKK AVEQRDFIGV DSTGKRLLFM ANEADLDEEL VIKGSILQKH PRIRFHTGLV DAHLYCLKKY IVDFLMENGS ITSIRSELIP YLVRKQFSSA SSQQGQEEKE EDLKKKELKS LDIYSFIKEA NTLNLAPYDA CWNACRGDRW EDLSRSQVRC YVHIMKEGLC SRVSTLGLYM EANRQVPKLL SALCPEEPPV HSSAQIVSKH LVGVDSLIGP ETQIGEKSSI KRSVIGSSCL IKDRVTITNC LLMNSVTVEE GSNIQGSVIC NNAVIEKGAD IKDCLIGSGQ RIEAKAKRVN EVIVGNDQLM EI

Frequently asked questions

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

Which diseases are associated with EIF2B3?

The strongest Open Targets associations for EIF2B3 are CACH syndrome, leukoencephalopathy with vanishing white matter, leukoencephalopathy with vanishing white matter 1, ovarioleukodystrophy and late infantile CACH syndrome.

How long is the EIF2B3 protein?

The Homo sapiens EIF2B3 protein (UniProt Q9NR50) is 452 amino acids long.

Browse: Targets: E · 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

UniProtQ9NR50
GeneEIF2B3
OrganismHomo sapiens
Length452
Binders0
Diseases61
View on UniProt