Research workbench
AlphaFold monomer V2.0 prediction for DNA-directed RNA polymerases I and III subunit RPAC1 (Q32L22)
Analyse AlphaFold monomer V2.0 prediction for DNA-directed RNA polymerases I and III… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- Accession
- Q32L22
- Type
- protein
- Length
- 346 residues
- Chains
- 1
- Collection
- MolNFT v1 / AlphaFold
- Contract
- 0xBf7491af3407816DFa88a5EA4c82e8A2B1D721eD
- Owner
- 0xb4D2d9c96b0D792d0b77e7147D724cc1F801ae58
- Molecule
- DNA-directed RNA polymerases I and III subunit RPAC1
- UniProt
- Q32L22
- Pockets
- 1 · best druggability 0.57
Structure
1 distinct chain · 29% helix, 34% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | DNA-directed RNA polymerases I and III subunit RPAC1 | protein | 346 | 29% helix, 34% strand | Q32L22 |
Pockets
1 pocket found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 267 | 0.57 | 0.77 | 20 | 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 Q32L22
- Elsewhere: UniProt Q32L22 · AlphaFold DB Q32L22
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