Research workbench
Crystal structure of the bb' fragment of ERP57
Analyse Crystal structure of the bb' fragment of ERP57 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 2H8L
- Type
- protein
- Length
- 694 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Protein disulfide-isomerase A3
- EC
- 5.3.4.1
- UniProt
- P30101
- Pockets
- 13 · best druggability 0.65
Structure
x-ray diffraction · 2 distinct chains · 36% helix, 20% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, C | Protein disulfide-isomerase A3 (EC 5.3.4.1) | protein | 232 | 36% helix, 20% strand | P30101 |
| B | Protein disulfide-isomerase A3 (EC 5.3.4.1) | protein | 230 | 35% helix, 20% strand | P30101 |
Pockets
13 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 576 | 0.65 | 0.76 | 48 | empty |
| 2 | 345 | 0.64 | 0.79 | 45 | empty |
| 3 | 166 | 0.63 | 0.85 | 32 | empty |
| 4 | 183 | 0.60 | 0.82 | 37 | empty |
| 5 | 295 | 0.57 | 0.77 | 25 | empty |
Interfaces
3 interfaces between chains.
- A–B · 669 Ų buried · 14 hydrogen bonds · protein-protein
- A–C · 355 Ų buried · 4 hydrogen bonds · protein-protein
- B–C · 166 Ų buried · 3 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 15 modified (engineered).
Compared structures
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 P30101
- Elsewhere: RCSB PDB 2H8L · PDBe 2H8L · UniProt P30101
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