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The crystal structure of sensory box histidine KINASE/RESPONSE regulator domain from chlorobium tepidum tls
Analyse The crystal structure of sensory box histidine KINASE/RESPONSE regulator domain… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3ICY
- Type
- protein
- Length
- 236 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Sensor protein
- EC
- 2.7.13.3
- UniProt
- Q8KAU2
- Pockets
- 3 · best druggability 0.52
Structure
x-ray diffraction · 1 distinct chain · 31% helix, 39% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | Sensor protein (EC 2.7.13.3) | protein | 118 | 31% helix, 39% strand | Q8KAU2 |
Ligands and binding sites
- GOL · Glycerol · additive · 4 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 255 | 0.52 | 0.75 | 33 | empty |
| 2 | 65 | 0.30 | 0.74 | 13 | empty |
| 3 | 68 | 0.27 | 0.72 | 15 | GOL |
Interfaces
1 interface between chains.
- A–B · 545 Ų buried · 3 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 6 modified (engineered).
Compared structures
- 3ICY · The crystal structure of sensory box histidine kinase/response regulator domain from… · the same entry in another collection · chain B against B, 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 Q8KAU2
- Elsewhere: RCSB PDB 3ICY · PDBe 3ICY · UniProt Q8KAU2
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