V0 assembly protein 1 (VOA1) is a 265-residue protein from Saccharomyces cerevisiae (strain ATCC 204508 / S288c). This is its AlphaFold structure prediction, created 1 Aug 2025. UniProt accession: P53262.
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The mean pLDDT of this model is 72.3 (confident overall). pLDDT is AlphaFold's per-residue confidence score from 0 to 100. In MolViewer, choose the B-factor color scheme to color the model by pLDDT, because AlphaFold stores it in the B-factor column.
| pLDDT band | Meaning | Share of residues |
|---|---|---|
| Above 90 | Very high: backbone and side chains are usually accurate | 16% |
| 70 to 90 | Confident: backbone generally right | 51% |
| 50 to 70 | Low: treat with caution | 16% |
| Below 50 | Very low: often disordered regions | 18% |
What pLDDT means and how to read it
Accessory component of the V0 complex of vacuolar(H+)-ATPase (V-ATPase), a multisubunit enzyme composed of a peripheral complex (V1) that hydrolyzes ATP and a membrane integral complex (V0) that translocates protons (PubMed:29526695). V-ATPase is responsible for acidifying and maintaining the pH of intracellular compartments (PubMed:29526695). Functions with VMA21 in assembly of the V0 complex (PubMed:18799613)
V-ATPase is a heteromultimeric enzyme composed of a peripheral catalytic V1 complex (components A to H) attached to an integral membrane V0 proton pore complex (components: a, c, c', c'', d, e, f and VOA1) (PubMed:29526695). Interacts with VMA21 (PubMed:18799613). Associates with the assembling V0 complex (PubMed:18799613)
Vacuole membrane, Endoplasmic reticulum membrane
Compare the prediction with experimentally determined structures of the same protein:
| PDB ID | Method | Resolution | Chains and residues |
|---|---|---|---|
| 8EAS | EM | 2.6 Å | b=1-265 |
| 6M0R | EM | 2.7 Å | N=212-263 |
| 7TAP | EM | 2.8 Å | N=1-265 |
| 6O7U | EM | 3.1 Å | b=1-265 |
| 6PE4 | EM | 3.1 Å | B=1-265 |
| 8EAT | EM | 3.1 Å | b=1-265 |
| 8EAU | EM | 3.1 Å | b=1-265 |
| 6O7T | EM | 3.2 Å | b=1-265 |
| 6PE5 | EM | 3.2 Å | B=1-265 |
| 7TAO | EM | 3.2 Å | N=1-265 |
| 9E7L | EM | 3.33 Å | N=1-265 |
| 9E76 | EM | 3.4 Å | N=1-265 |
| 6C6L | EM | 3.5 Å | N=1-265 |
| 7TMR | EM | 3.5 Å | b=1-265 |
| 6M0S | EM | 3.6 Å | N=212-263 |
| 9MJ4 | EM | 3.7 Å | N=1-265 |
| 7TMS | EM | 3.8 Å | b=1-265 |
| 7TMT | EM | 3.8 Å | b=1-265 |
| 7FDA | EM | 4.2 Å | e=1-265 |
| 7FDB | EM | 4.8 Å | e=1-265 |
Showing 20 of 24 experimental structures (best resolution first).
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