Research workbench
Crystal structure of the choline binding domain of SPR1274 in streptococcus pneumoniae
Analyse Crystal structure of the choline binding domain of SPR1274 in streptococcus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3HIA
- Type
- protein
- Length
- 223 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Choline binding protein
- UniProt
- Q8DP99
- Ligands
- PC, SO4
- Pockets
- 3 · best druggability 0.69
Structure
x-ray diffraction · 3 distinct chains · 0% helix, 48% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Choline binding protein | protein | 66 | 0% helix, 50% strand | Q8DP99 |
| B | Choline binding protein | protein | 83 | 0% helix, 51% strand | Q8DP99 |
| C | Choline binding protein | protein | 74 | 0% helix, 45% strand | Q8DP99 |
Ligands and binding sites
- PC · Phosphocholine · ligand · 7 copies · chains A, B, C
- SO4 · Sulfate ion · ion · 3 copies · chains A, B, C
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 354 | 0.69 | 0.82 | 43 | PC, SO4 |
| 2 | 249 | 0.62 | 0.81 | 30 | PC |
| 3 | 83 | 0.38 | 0.77 | 12 | PC |
Interfaces
3 interfaces between chains.
- A–B · 653 Ų buried · 9 hydrogen bonds · protein-protein
- A–C · 404 Ų buried · 4 hydrogen bonds · protein-protein
- B–C · 370 Ų buried · 5 hydrogen bonds · protein-protein
Compared structures
- 3HIA · Crystal structure of the choline binding domain of Spr1274 in Streptococcus pneumoniae · 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 Q8DP99
- Elsewhere: RCSB PDB 3HIA · PDBe 3HIA · UniProt Q8DP99
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