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The crystal structure of a tetr transcription regulator from silicibacter pomeroyi dss
Analyse The crystal structure of a tetr transcription regulator from silicibacter… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3DPJ
- Type
- protein
- Length
- 1,530 residues
- Chains
- 8
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Transcription regulator, tetr family
- UniProt
- Q5LS67
- Pockets
- 17 · best druggability 0.74
Structure
x-ray diffraction · 4 distinct chains · 77% helix, 0% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, C | Transcription regulator, tetr family | protein | 194 | 79% helix, 1% strand | Q5LS67 |
| B, D | Transcription regulator, tetr family | protein | 190 | 74% helix, 0% strand | Q5LS67 |
| E, G | Transcription regulator, tetr family | protein | 193 | 79% helix, 0% strand | Q5LS67 |
| F, H | Transcription regulator, tetr family | protein | 188 | 76% helix, 0% strand | Q5LS67 |
Ligands and binding sites
- EDO · 1,2-ethanediol · additive · 30 copies · chains A, F, B, C, H, D, G, E
- MES · 2-(N-morpholino)-ethanesulfonic acid · additive · 8 copies · chains A, B, C, D, E, F, G, H
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
17 pockets found on a 1 Å grid, 15 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 135 | 0.74 | 0.93 | 33 | EDO |
| 2 | 864 | 0.73 | 0.78 | 73 | EDO |
| 3 | 280 | 0.73 | 0.86 | 24 | MES |
| 4 | 826 | 0.73 | 0.78 | 71 | EDO |
| 5 | 267 | 0.71 | 0.85 | 26 | MES, EDO |
Interfaces
14 interfaces between chains.
- E–F · 1627 Ų buried · 23 hydrogen bonds · protein-protein
- G–H · 1617 Ų buried · 18 hydrogen bonds · protein-protein
- C–D · 1558 Ų buried · 16 hydrogen bonds · protein-protein
- A–B · 1555 Ų buried · 16 hydrogen bonds · protein-protein
- D–G · 385 Ų buried · 8 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 52 modified (engineered).
Compared structures
- 3DPJ · The crystal structure of a TetR transcription regulator from Silicibacter pomeroyi DSS · 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 Q5LS67
- Elsewhere: RCSB PDB 3DPJ · PDBe 3DPJ · UniProt Q5LS67
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