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Leiomodin-3 (LMOD3)

Homo sapiens — UniProt Q0VAK6

Gene: LMOD3Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Leiomodin-3 (LMOD3) is a protein from Homo sapiens identified by UniProt accession Q0VAK6, 560 residues long. MolForge cross-references it against 0 known binders and 200 disease associations.

  • UniProt accession: Q0VAK6; gene symbol LMOD3.
  • Organism: Homo sapiens.
  • Length: 560 amino acids.
  • Top disease associations (Open Targets): nemaline myopathy, typical nemaline myopathy and severe congenital nemaline myopathy.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameLeiomodin-3
UniProt accessionQ0VAK6
GeneLMOD3
OrganismHomo sapiens
Length560 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 (200)

Diseases linked to this target (Open Targets).

  • nemaline myopathy · score 0.77
  • typical nemaline myopathy · score 0.37
  • severe congenital nemaline myopathy · score 0.37
  • genetic disorder · score 0.19
  • mean corpuscular volume · score 0.17
  • mean corpuscular hemoglobin · score 0.14
  • mean corpuscular hemoglobin concentration · score 0.13
  • celiac disease · score 0.10
  • cortical surface area measurement · score 0.09
  • Malabsorption · score 0.08

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q0VAK6-F1alphafoldPREDICTED67.81—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q0VAK6.

Amino-acid sequence (560 residues)

MSEHSRNSDQ EELLDEEINE DEILANLSAE ELKELQSEME VMAPDPSLPV GMIQKDQTDK PPTGNFNHKS LVDYMYWEKA SRRMLEEERV PVTFVKSEEK TQEEHEEIEK RNKNMAQYLK EKLNNEIVAN KRESKGSSNI QETDEEDEEE EDDDDDDEGE DDGEESEETN REEEGKAKEQ IRNCENNCQQ VTDKAFKEQR DRPEAQEQSE KKISKLDPKK LALDTSFLKV STRPSGNQTD LDGSLRRVRK NDPDMKELNL NNIENIPKEM LLDFVNAMKK NKHIKTFSLA NVGADENVAF ALANMLRENR SITTLNIESN FITGKGIVAI MRCLQFNETL TELRFHNQRH MLGHHAEMEI ARLLKANNTL LKMGYHFELP GPRMVVTNLL TRNQDKQRQK RQEEQKQQQL KEQKKLIAML ENGLGLPPGM WELLGGPKPD SRMQEFFQPP PPRPPNPQNV PFSQRSEMMK KPSQAPKYRT DPDSFRVVKL KRIQRKSRMP EAREPPEKTN LKDVIKTLKP VPRNRPPPLV EITPRDQLLN DIRHSSVAYL KPVQLPKELA

Frequently asked questions

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

Which diseases are associated with LMOD3?

The strongest Open Targets associations for LMOD3 are nemaline myopathy, typical nemaline myopathy, severe congenital nemaline myopathy, genetic disorder and mean corpuscular volume.

How long is the LMOD3 protein?

The Homo sapiens LMOD3 protein (UniProt Q0VAK6) is 560 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

UniProtQ0VAK6
GeneLMOD3
OrganismHomo sapiens
Length560
Binders0
Diseases200
View on UniProt