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LETM1 domain-containing protein LETM2, mitochondrial (LETM2)

Homo sapiens — UniProt Q2VYF4

Gene: LETM2Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

LETM1 domain-containing protein LETM2, mitochondrial (LETM2) is a protein from Homo sapiens identified by UniProt accession Q2VYF4, 491 residues long. MolForge cross-references it against 0 known binders and 50 disease associations.

  • UniProt accession: Q2VYF4; gene symbol LETM2.
  • Organism: Homo sapiens.
  • Length: 491 amino acids.
  • Top disease associations (Open Targets): neurodegenerative disease, appendicular lean mass and lysosomal storage disease.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameLETM1 domain-containing protein LETM2, mitochondrial
UniProt accessionQ2VYF4
GeneLETM2
OrganismHomo sapiens
Length491 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 (50)

Diseases linked to this target (Open Targets).

  • neurodegenerative disease · score 0.35
  • appendicular lean mass · score 0.26
  • lysosomal storage disease · score 0.23
  • Parkinson disease · score 0.23
  • Alzheimer disease · score 0.23
  • multiple sclerosis · score 0.23
  • Red cell distribution width · score 0.18
  • lean body mass · score 0.17
  • lymphocyte count · score 0.16
  • mean platelet volume · score 0.14

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q2VYF4-F1alphafoldPREDICTED61.84—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q2VYF4.

Amino-acid sequence (491 residues)

MAFYSYNSVL AIARTRFPSH FVHPTCSSYS PSCAFLHLPD SHLNKTCMKN YESKKYSDPS QPGNTVLHPG TRLIQKLHTS TCWLQEVPGK PQLEQATKHP QVTSPQATKE TGMEIKEGKQ SYRQKIMDEL KYYYNGFYLL WIDAKVAARM VWRLLHGQVL TRRERRRLLR TCVDFFRLVP FMVFLIVPFM EFLLPVFLKL FPEMLPSTFE SESKKEEKQK KKMAVKLELA KFLQETMTEM ARRNRAKMGD ASTQLSSYVK QVQTGHKPST KEIVRFSKLF EDQLALEHLD RPQLVALCKL LELQTFGTNN LLRFQLLMKL KSIKADDEII AKEGVTALSV SELQAACRAR GMRSLGLTEE QLRQQLTEWQ DLHLKENVPP SLLLLSRTFY LIDVKPKPIE IPLSGEAPKT DILVELPTFT ESKENMVDLA PQLKGTKDED FIQPPPVTSS PITPSTPISL PKGPITSSEE PTLQAKSQMT AQNSKASSKG A

Frequently asked questions

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

Which diseases are associated with LETM2?

The strongest Open Targets associations for LETM2 are neurodegenerative disease, appendicular lean mass, lysosomal storage disease, Parkinson disease and Alzheimer disease.

How long is the LETM2 protein?

The Homo sapiens LETM2 protein (UniProt Q2VYF4) is 491 amino acids long.

Browse: Targets: L · 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

UniProtQ2VYF4
GeneLETM2
OrganismHomo sapiens
Length491
Binders0
Diseases50
View on UniProt