Myosin-2 (MYH2)
Homo sapiens — UniProt Q9UKX2
Data last refreshed: (UniProt release unknown)
Key facts
Myosin-2 (MYH2) is a protein from Homo sapiens identified by UniProt accession Q9UKX2, 1941 residues long. MolForge cross-references it against 0 known binders and 104 disease associations.
- UniProt accession: Q9UKX2; gene symbol MYH2.
- Organism: Homo sapiens.
- Length: 1941 amino acids.
- Top disease associations (Open Targets): myopathy, proximal, and ophthalmoplegia, inclusion body myositis and childhood-onset autosomal recessive myopathy with external ophthalmoplegia.
- 3D structure: AlphaFold model available.
Target properties
| Protein name | Myosin-2 |
|---|---|
| UniProt accession | Q9UKX2 |
| Gene | MYH2 |
| Organism | Homo sapiens |
| Length | 1941 residues |
| Molecular weight | — |
| EC numbers | — |
| Target class | — |
| Subcellular location | — |
| Keywords | — |
Druggability
Target tractability assessment (Open Targets + pocket analysis). No approved drug
| Druggability tier | MEDIUM |
|---|---|
| Druggability score | — |
| Pocket score | — |
| Max clinical phase | — |
Disease associations (104)
Diseases linked to this target (Open Targets).
- myopathy, proximal, and ophthalmoplegia · score 0.78
- inclusion body myositis · score 0.57
- childhood-onset autosomal recessive myopathy with external ophthalmoplegia · score 0.44
- hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome · score 0.44
- Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia · score 0.37
- cutaneous Leishmaniasis · score 0.37
- myopathy · score 0.33
- genetic disorder · score 0.19
- glioblastoma multiforme · score 0.18
- endometrial cancer · score 0.18
3D Structure (1)
Experimental (PDB) and predicted (AlphaFold) structures for this protein.
| Structure | Source | Method | Mean pLDDT | Resolution (Å) |
|---|---|---|---|---|
| AF-Q9UKX2-F1 | alphafold | PREDICTED | 73.31 | — |
Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9UKX2.
Amino-acid sequence (1941 residues)
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
Which diseases are associated with MYH2?
The strongest Open Targets associations for MYH2 are myopathy, proximal, and ophthalmoplegia, inclusion body myositis, childhood-onset autosomal recessive myopathy with external ophthalmoplegia, hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome and Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia.
How long is the MYH2 protein?
The Homo sapiens MYH2 protein (UniProt Q9UKX2) is 1941 amino acids long.
Browse: Targets: M · all protein targets A–Z · drugs A–Z.
Sources
- UniProtKB Q9UKX2 — name, gene, function, sequence, keywords (CC BY 4.0)
- AlphaFold DB Q9UKX2 — predicted 3D structure (CC BY 4.0)
- Open Targets Platform — disease associations and tractability (CC0)
How this page is built: methodology · editorial policy & corrections.
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