Research workbench
AlphaFold monomer V2.0 prediction for DNA replication terminus site- binding protein (Q57PG8)
Analyse AlphaFold monomer V2.0 prediction for DNA replication terminus site- binding… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- Accession
- Q57PG8
- Type
- protein
- Length
- 309 residues
- Chains
- 1
- Collection
- MolNFT v1 / AlphaFold
- Contract
- 0xBf7491af3407816DFa88a5EA4c82e8A2B1D721eD
- Owner
- 0x4F3500FD13628563884A773578190b4E4dCd3a28
- Molecule
- DNA replication terminus site-binding protein
- UniProt
- Q57PG8
- Pockets
- 4 · best druggability 0.60
Structure
1 distinct chain · 39% helix, 27% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | DNA replication terminus site-binding protein | protein | 309 | 39% helix, 27% strand | Q57PG8 |
Pockets
4 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 292 | 0.60 | 0.79 | 34 | empty |
| 2 | 117 | 0.40 | 0.75 | 23 | empty |
| 3 | 97 | 0.32 | 0.73 | 15 | empty |
| 4 | 79 | 0.32 | 0.73 | 11 | empty |
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt Q57PG8
- Elsewhere: UniProt Q57PG8 · AlphaFold DB Q57PG8
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