Research workbench
Crystal structure of mcsg target APC27401 from shigella flexneri
Analyse Crystal structure of mcsg target APC27401 from shigella flexneri in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1Y2I
- Type
- protein
- Length
- 545 residues
- Chains
- 5
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Hypothetical protein S0862
- UniProt
- Q83LS2
- Pockets
- 6 · best druggability 0.85
Structure
x-ray diffraction · 1 distinct chain · 28% helix, 44% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C, D, E | Hypothetical protein S0862 | protein | 109 | 28% helix, 44% strand | Q83LS2 |
Pockets
6 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1103 | 0.85 | 0.87 | 97 | empty |
| 2 | 103 | 0.39 | 0.75 | 13 | empty |
| 3 | 105 | 0.38 | 0.75 | 18 | empty |
| 4 | 90 | 0.36 | 0.75 | 14 | empty |
| 5 | 87 | 0.34 | 0.74 | 15 | empty |
Interfaces
5 interfaces between chains.
- D–E · 1468 Ų buried · 28 hydrogen bonds · protein-protein
- A–E · 1461 Ų buried · 23 hydrogen bonds · protein-protein
- C–D · 1448 Ų buried · 26 hydrogen bonds · protein-protein
- A–B · 1442 Ų buried · 26 hydrogen bonds · protein-protein
- B–C · 1441 Ų buried · 24 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 Q83LS2
- Elsewhere: RCSB PDB 1Y2I · PDBe 1Y2I · UniProt Q83LS2
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