Research workbench
AlphaFold monomer V2.0 prediction for polyribonucleotide nucleotidyltransferase (Q89AF8)
Analyse AlphaFold monomer V2.0 prediction for polyribonucleotide nucleotidyltransferase… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- Accession
- Q89AF8
- Type
- protein
- Length
- 693 residues
- Chains
- 1
- Collection
- MolNFT v1 / AlphaFold
- Contract
- 0xBf7491af3407816DFa88a5EA4c82e8A2B1D721eD
- Owner
- 0x8DD273cF423965BB2D13d0c9e489307D68b23f90
- Molecule
- Polyribonucleotide nucleotidyltransferase
- UniProt
- Q89AF8
- Pockets
- 5 · best druggability 0.75
Structure
1 distinct chain · 35% helix, 30% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Polyribonucleotide nucleotidyltransferase | protein | 693 | 35% helix, 30% strand | Q89AF8 |
Pockets
5 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 858 | 0.75 | 0.79 | 82 | empty |
| 2 | 899 | 0.70 | 0.76 | 85 | empty |
| 3 | 54 | 0.33 | 0.77 | 17 | empty |
| 4 | 60 | 0.30 | 0.75 | 15 | empty |
| 5 | 58 | 0.28 | 0.74 | 18 | 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 Q89AF8
- Elsewhere: UniProt Q89AF8 · AlphaFold DB Q89AF8
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