Research workbench
Crystal structure of dnde from escherichia COLI B7A involved in DNA phosphorothioation modification
Analyse Crystal structure of dnde from escherichia COLI B7A involved in DNA… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4LRV
- Type
- protein
- Length
- 1,675 residues
- Chains
- 16
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- DNA sulfur modification protein dnde
- UniProt
- B3HI59
- Pockets
- 20 · best druggability 0.86
Structure
x-ray diffraction · 12 distinct chains · 62% helix, 5% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, D | DNA sulfur modification protein dnde | protein | 107 | 58% helix, 6% strand | B3HI59 |
| B, J | DNA sulfur modification protein dnde | protein | 106 | 62% helix, 6% strand | B3HI59 |
| C | DNA sulfur modification protein dnde | protein | 105 | 62% helix, 4% strand | B3HI59 |
| E | DNA sulfur modification protein dnde | protein | 102 | 65% helix, 5% strand | B3HI59 |
| F | DNA sulfur modification protein dnde | protein | 104 | 63% helix, 5% strand | B3HI59 |
| G, H, O | DNA sulfur modification protein dnde | protein | 106 | 62% helix, 4% strand | B3HI59 |
| I | DNA sulfur modification protein dnde | protein | 102 | 64% helix, 4% strand | B3HI59 |
| K | DNA sulfur modification protein dnde | protein | 104 | 63% helix, 5% strand | B3HI59 |
| L | DNA sulfur modification protein dnde | protein | 100 | 64% helix, 4% strand | B3HI59 |
| M | DNA sulfur modification protein dnde | protein | 106 | 60% helix, 5% strand | B3HI59 |
| N | DNA sulfur modification protein dnde | protein | 104 | 63% helix, 5% strand | B3HI59 |
| P | DNA sulfur modification protein dnde | protein | 104 | 62% helix, 6% strand | B3HI59 |
Pockets
20 pockets found on a 1 Å grid, 12 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1078 | 0.86 | 0.87 | 109 | empty |
| 2 | 919 | 0.85 | 0.86 | 84 | empty |
| 3 | 705 | 0.80 | 0.84 | 90 | empty |
| 4 | 405 | 0.72 | 0.83 | 63 | empty |
| 5 | 190 | 0.68 | 0.86 | 35 | empty |
Interfaces
40 interfaces between chains.
- A–M · 720 Ų buried · 12 hydrogen bonds · protein-protein
- B–K · 705 Ų buried · 9 hydrogen bonds · protein-protein
- N–O · 677 Ų buried · 13 hydrogen bonds · protein-protein
- F–P · 660 Ų buried · 10 hydrogen bonds · protein-protein
- I–J · 641 Ų buried · 11 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 48 modified (engineered).
Compared structures
- 4LRV · Crystal structure of DndE from Escherichia coli B7A involved in DNA phosphorothioation… · the same entry in another collection · chain A against A, TM-score 1.00
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 B3HI59
- Elsewhere: RCSB PDB 4LRV · PDBe 4LRV · UniProt B3HI59
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