Research workbench
Structure of the C-terminal domains of dipz from mycobacterium tuberculosis
Analyse Structure of the C-terminal domains of dipz from mycobacterium tuberculosis in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5CYY
- Type
- protein
- Length
- 1,325 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Protein dipz
- UniProt
- P9WG63
- Pockets
- 7 · best druggability 0.77
Structure
x-ray diffraction · 3 distinct chains · 20% helix, 35% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, C | Protein dipz | protein | 333 | 20% helix, 35% strand | P9WG63 |
| B | Protein dipz | protein | 328 | 20% helix, 35% strand | P9WG63 |
| D | Protein dipz | protein | 331 | 20% helix, 35% strand | P9WG63 |
Pockets
7 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 483 | 0.77 | 0.85 | 70 | empty |
| 2 | 461 | 0.75 | 0.84 | 56 | empty |
| 3 | 161 | 0.61 | 0.84 | 21 | empty |
| 4 | 166 | 0.60 | 0.84 | 30 | empty |
| 5 | 202 | 0.48 | 0.75 | 32 | empty |
Interfaces
4 interfaces between chains.
- C–D · 2227 Ų buried · 34 hydrogen bonds · protein-protein
- A–B · 2127 Ų buried · 36 hydrogen bonds · protein-protein
- A–C · 203 Ų buried · 2 hydrogen bonds · protein-protein
- A–D · 135 Ų buried · 1 hydrogen bond · protein-protein
Modifications
Observed in the structure: 6 disulfide (disulfide).
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 P9WG63
- Elsewhere: RCSB PDB 5CYY · PDBe 5CYY · UniProt P9WG63
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