Research workbench
AlphaFold monomer V2.0 prediction for peptidyl-tRNA hydrolase (B2S1C9)
Analyse AlphaFold monomer V2.0 prediction for peptidyl-tRNA hydrolase (B2S1C9) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- Accession
- B2S1C9
- Type
- protein
- Length
- 188 residues
- Chains
- 1
- Collection
- MolNFT v1 / AlphaFold
- Contract
- 0xBf7491af3407816DFa88a5EA4c82e8A2B1D721eD
- Owner
- 0x6DAA77C4263E74E745cA9c4D8E291e57e8991Cf5
- Molecule
- Peptidyl-tRNA hydrolase
- UniProt
- B2S1C9
- Pockets
- 2 · best druggability 0.55
Structure
1 distinct chain · 42% helix, 23% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Peptidyl-tRNA hydrolase | protein | 188 | 42% helix, 23% strand | B2S1C9 |
Pockets
2 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 77 | 0.55 | 0.86 | 18 | empty |
| 2 | 122 | 0.44 | 0.77 | 27 | 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 B2S1C9
- Elsewhere: UniProt B2S1C9 · AlphaFold DB B2S1C9
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