Research workbench
Mycobacterium tuberculosis lexa C-domain II
Analyse Mycobacterium tuberculosis lexa C-domain II in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6A2R
- Type
- protein
- Length
- 594 residues
- Chains
- 6
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Lexa repressor
- EC
- 3.4.21.88
- UniProt
- P9WHR7
- Pockets
- 1 · best druggability 0.33
Structure
x-ray diffraction · 1 distinct chain · 9% helix, 41% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C, D, E, F | Lexa repressor (EC 3.4.21.88) | protein | 99 | 9% helix, 41% strand | P9WHR7 |
Ligands and binding sites
- PEG · Di(hydroxyethyl)ether · additive · 2 copies · chains A, B, C, D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
1 pocket found on a 1 Å grid, 0 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 96 | 0.33 | 0.73 | 18 | empty |
Interfaces
7 interfaces between chains.
- C–D · 1316 Ų buried · 14 hydrogen bonds · protein-protein
- E–F · 1306 Ų buried · 14 hydrogen bonds · protein-protein
- A–B · 1290 Ų buried · 14 hydrogen bonds · protein-protein
- C–E · 215 Ų buried · 3 hydrogen bonds · protein-protein
- A–C · 121 Ų buried · 3 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 6 modified (artifact).
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 P9WHR7
- Elsewhere: RCSB PDB 6A2R · PDBe 6A2R · UniProt P9WHR7
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